Locus Specific Mutation Databases |
|
Genes are in order of HUGO
APPROVED GENE DESIGNATION not alias. e.g. "p53" will be found
under "TP53" while "CD40L" or "TNFSF5" will be found under "CD40LG"
and so on.
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Please select the first letter of the Gene: | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | ||
OR | ||||||||||||||||||||||||||||
Specify the HGNC Gene Symbol: |
HGNC GENE SYMBOL OMIM NO. |
DATABASE NAME
INTERNET ADDRESS |
CURATORS |
Go Back To Main Index! | ||
ABCA12
ATP-binding cassette, sub-family A (ABC1), member 12 607800 |
Mutations of the ATP-binding Cassette Transporter A 12 (ABCA12) associated with harlequin ichthyosis, congenital ichthyosiform erythroderma and lamellar ichthyosis
http://www.derm-hokudai.jp/ABCA12/ |
Masashi Akiyama and Kaori Sakai |
ABCA13
ATP-binding cassette, sub-family A (ABC1), member 13 607807 |
LOVD - Leiden Open Variation Database
http://www.LOVD.nl/ABCA13 |
Johan T. den Dunnen and Ben Pickard |
ABCA4
ATP-binding cassette, sub-family A (ABC1), member 4 601691 |
Mutations of the ATP-binding Cassette Transporter Retina
http://www.retina-international.org/sci-news/abcrmut.htm |
Retina International |
ABCB11
ATP-binding cassette, sub-family B (MDR/TAP), member 11 603201 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ABCB11 |
Ammar Husami |
ABCB4
ATP-binding cassette, sub-family B (MDR/TAP), member 4 171060 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ABCB4 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
ABCB7
ATP-binding cassette, sub-family B (MDR/TAP), member 7 300135 |
ABCB7 database at LOVD
http://www.LOVD.nl/ABCB7 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ABCC6
ATP-binding cassette, sub-family C (CFTR/MRP), member 6 603234 |
Mutations of the Multidrug Resistance-associated Protein 6 (ABCC6/ MPR6/ MOAT-E)
http://www.retina-international.org/sci-news/abcc6mut.htm |
Retina International |
ABCC6
ATP-binding cassette, sub-family C (CFTR/MRP), member 6 603234 |
LOVD at NCBI
http://www.ncbi.nlm.nih.gov/lovd/home.php?select_db=ABCC6 |
Sharon Terry and Tim Hefferon |
ABCD1
ATP-binding cassette, sub-family D (ALD), member 1 300371 |
X-linked Adrenoleukodystrophy Database
http://www.x-ald.nl |
Hugo W. Moser Dept. of Neurogenetics Kennedy Krieger Inst. Baltimore, USA. Stephan Kemp, Ronald R.J.A. Wanders Lab. of Genetic Metabolic Diseases Academic Medical Ctr. Amsterdam, The Netherlands. |
ABO
ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 110300 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
ACAD8
acyl-CoA dehydrogenase family, member 8 604773 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=ACAD8 |
Steafnie Kalb |
ACADM
acyl-CoA dehydrogenase, C-4 to C-12 straight chain 607008 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ACADM |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
ACADSB
acyl-CoA dehydrogenase, short/branched chain 600301 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=ACADSB |
Stefanie Kalb |
ACADVL
acyl-CoA dehydrogenase, very long chain 609575 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ACADVL |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
ACE2
angiotensin I converting enzyme (peptidyl-dipeptidase A) 2 300335 |
ACE2 database at LOVD
http://www.LOVD.nl/ACE2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ACHE
acetylcholinesterase (Yt blood group) 100740 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
ACOT9
acyl-CoA thioesterase 9 |
ACOT9 database at LOVD
http://www.LOVD.nl/ACOT9 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ACSL4
acyl-CoA synthetase long-chain family member 4 300157 |
ACSL4 database at LOVD
http://www.LOVD.nl/ACSL4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ACTA1
actin, alpha 1, skeletal muscle 102610 |
Laing Laboratory Skeletal muscle alpha-actin (ACTA1)
http://acta1.waimr.uwa.edu.au/home.php?select_db=ACTA1 |
Nigel Laing and Kristen Nowak |
ACTA1
actin, alpha 1, skeletal muscle 102610 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/ACTA1 |
Kristen Nowak and Nigel Laing |
ACTC1
actin, alpha, cardiac muscle 1 102540 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent. Dept. Mol & Clin Genet. Royal Prince Alfred Hosp. Sydney, Australia |
ACTC1
actin, alpha, cardiac muscle 1 102540 |
Sarcomere Protein Gene Mutation Database
http://genetics.med.harvard.edu/%7Eseidman/cg3/genes/ACTC_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School. |
ACTRT1
actin-related protein T1 300487 |
ACTRT1 database at LOVD
http://www.LOVD.nl/ACTRT1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ACVRL1
activin A receptor type II-like 1 601284 |
Hereditary Hemorrhagic Telangiectasia (HHT) Mutation Database
http://www.hhtmutation.org/ |
Paul Westwood, The Molecular Genetics Service, Edinburgh, UK |
ADA
adenosine deaminase 608958 |
ADAbase: Mutation registry for Adenosine Deaminase Deficiency
http://bioinf.uta.fi/ADAbase/ |
Mauno Vihinen, Michael Hershfield, Univ. of Tampere, Finland |
ADSL
adenylosuccinate lyase 608222 |
Adenylosuccinate Lyase Mutations Database Home Page
http://www.icp.ucl.ac.be/adsldb/ |
Georges Van Den Berghe, Christian De Duve Instutute for Cellular Pathology (ICP), University of Louvain Medical School, Belgium |
AFF2
AF4/FMR2 family, member 2 309548 |
AFF2 database at LOVD
http://www.LOVD.nl/AFF2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AGRN
agrin 103320 |
AGRN - Leiden Muscular Dystrophy pages
http://www.LOVD.nl/AGRN |
ddunnen@LUMC.nl, tom.winder@preventiongenetics.com |
AGTR2
angiotensin II receptor, type 2 300034 |
AGTR2 database at LOVD
http://www.LOVD.nl/AGTR2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AICDA
activation-induced cytidine deaminase 605257 |
AICDA base: Mutation registry for Aid deficiency
http://bioinf.uta.fi/AICDAbase/ |
Anne Durandy, Mauno Vihinen, Univ. of Tampere, Finland |
AIFM1
apoptosis-inducing factor, mitochondrion-associated, 1 300169 |
AIFM1 database at LOVD
http://www.LOVD.nl/AIFM1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AIPL1
aryl hydrocarbon receptor interacting protein-like 1 604392 |
Mutations of the Aryl Hydrocarbon Receptor-interacting Protein-like 1
http://www.retina-international.org/sci-news/aipl1mut.htm |
Retina International |
AIRE
autoimmune regulator 607358 |
AIREbase: Mutation registry for APECED
http://bioinf.uta.fi/AIREbase/ |
Mauno Vihinen, P�rt Peterson, Univ. of Tampere, Finland |
AKAP14
A kinase (PRKA) anchor protein 14 300462 |
AKAP14 database at LOVD
http://www.LOVD.nl/AKAP14 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AKAP4
A kinase (PRKA) anchor protein 4 300185 |
AKAP4 database at LOVD
http://www.LOVD.nl/AKAP4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AKAP9
A kinase (PRKA) anchor protein (yotiao) 9 604001 |
Zhejiang University-Adinovo Center AKAP9 Database
http://www.china-hvp.org/LOVD/?select_db=AKAP9 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
ALB
albumin 103600 |
Albumin mutation database
http://www.albumin.org/ |
Prof. Ulrich Kragh-Hansen, University of Aarhus, Aarhus, Denmark, and Dr. Theodore Peters, Jr., Bassett Healthcare, Cooperstown, NY, USA |
ALDH1A1
aldehyde dehydrogenase 1 family, member A1 100640 |
Human Polymorphisms of ALDH Genes
http://www.aldh.org |
Vasilis Vasiliou, Agi Pappa, Univ. Colorado Health Sci. Center, Denver, U.S.A. |
ALDH2
aldehyde dehydrogenase 2 family (mitochondrial) 100650 |
Human Polymorphisms of ALDH Genes
http://www.aldh.org |
Vasilis Vasiliou, Agi Pappa, Univ. Colorado Health Sci. Center, Denver, U.S.A. |
ALDH3A1
aldehyde dehydrogenase 3 family, member A1 100660 |
Human Polymorphisms of ALDH Genes
http://www.aldh.org/ |
Vasilis Vasiliou, Agi Pappa, Univ. Colorado Health Sci. Center, Denver, U.S.A. |
ALDH4A1
aldehyde dehydrogenase 4 family, member A1 606811 |
Human Polymorphisms of ALDH Genes
http://www.aldh.org/ |
Vasilis Vasiliou, Agi Pappa, Univ. Colorado Health Sci. Center, Denver, U.S.A. |
ALDH5A1
aldehyde dehydrogenase 5 family, member A1 610045 |
Succinic semialdehyde dehydrogenase (ALDH5A1) Variation Database
http://www.lovd.nl/ALDH5A1 |
Gajja Salomons |
ALDH7A1
aldehyde dehydrogenase 7 family, member A1 107323 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
ALDH9A1
aldehyde dehydrogenase 9 family, member A1 602733 |
Human Polymorphisms of ALDH Genes
http://www.aldh.org |
Vasilis Vasiliou, Agi Pappa Univ. Colorado Health Sci. Center, Denver, U.S.A. |
ALDOB
aldolase B, fructose-bisphosphate 229600 |
Hereditary Fructose Intolerance/Aldolase
http://www.bu.edu/aldolase/ |
Dean R. Tolan, Boston Univ., U.S.A. |
ALG1
asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog (S. cerevisiae) 605907 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs Center for Human Genetics Leuven, Belgium |
ALG12
asparagine-linked glycosylation 12, alpha-1,6-mannosyltransferase homolog (S. cerevisiae) 607144 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALG13
asparagine-linked glycosylation 13 homolog (S. cerevisiae) 300776 |
ALG13 database at LOVD
http://www.LOVD.nl/ALG13 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ALG2
asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog (S. cerevisiae) 607905 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALG3
asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae) 608750 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALG6
asparagine-linked glycosylation 6, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) 604566 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALG8
asparagine-linked glycosylation 8, alpha-1,3-glucosyltransferase homolog (S. cerevisiae) 608103 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALG9
asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog (S. cerevisiae) 606941 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
ALOX5AP
arachidonate 5-lipoxygenase-activating protein 603700 |
arachidonate 5-Lipoxygenase-activating protein (ALOX5AP) database
http://lovd.bx.psu.edu/home.php?select_db=ALOX5AP |
Belinda Giardine and Joseph Borg |
ALPL
alkaline phosphatase, liver/bone/kidney 171760 |
Tissue Nonspecific Alkaline Phosphatase Gene Mutation Database
http://www.sesep.uvsq.fr/Database.html |
Etienne Mornet, Laboratoire SESEP, Universite de Versailles, Versailles, France |
AMELX
amelogenin, X-linked 300391 |
AMELX database at LOVD
http://www.LOVD.nl/AMELX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AMMECR1
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 300195 |
AMMECR1 database at LOVD
http://www.LOVD.nl/AMMECR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AMOT
angiomotin 300410 |
AMOT database at LOVD
http://www.LOVD.nl/AMOT |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ANK2
ankyrin 2, neuronal 106410 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
ANK2
ankyrin 2, neuronal 106410 |
Zhejiang University-Adinovo Center ANK2 Database
http://www.china-hvp.org/LOVD/?select_db=ANK2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
ANO5
anoctamin 5 608662 |
ANO5 - Leiden Muscular Dystrophy pages
http://www.LOVD.nl/ANO5 |
Johan T. den Dunnen Leiden Univ. Med Centre |
ANO5
anoctamin 5 608662 |
ANO5 LOVD - Leiden Open Variation Database
http://www.medgen.mcgill.ca/ANO5/home.php?select_db=ANO5 |
V�ronique Bolduc |
AP1S2
adaptor-related protein complex 1, sigma 2 subunit 300629 |
AP1S2 database at LOVD
http://www.LOVD.nl/AP1S2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AP3B1
adaptor-related protein complex 3, beta 1 subunit 603401 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting Int. Albinism Centre Univ. of Minnesota, U.S.A. |
AP3B1
adaptor-related protein complex 3, beta 1 subunit 603401 |
AP3B1base: Mutation registry for Hermansky-Pudlak syndrome 2
http://bioinf.uta.fi/AP3B1base/ |
Mauno Vihinen, Univ. of Tampere, Finland |
AP3B1
adaptor-related protein complex 3, beta 1 subunit 603401 |
Mutations of the Adaptin b3a Gene
http://www.retina-international.org/sci-news/adtb3mut.htm |
Retina International |
APC
adenomatous polyposis coli 611731 |
The UMD APC mutations database
http://www.umd.be/APC/ |
Christophe Beroud, Laboratoire de g�n�tique Mol�culaire et Chromosomique, Montpellier, France Thierry Soussi INSERM, Hopital Necker Enfants Malades, Paris |
APC
adenomatous polyposis coli 611731 |
APC-Database
http://www.LOVD.nl/APC |
Dr. Stefan Aretz and Dr. Waltraut Friedl |
APC
adenomatous polyposis coli 611731 |
Zhejiang University-Adinovo Center APC Database
http://china-hvp.org/LOVD/?select_db=APC |
Ming Qi, PhD, FACMG, Peikuan Cong and Yudong Gao |
APC
adenomatous polyposis coli 611731 |
The APC Mutation Database
http://fap.taenzer.me |
Dr. Stefan Aretz and Dr. Waltraut Friedl |
APEX2
APEX nuclease (apurinic/apyrimidinic endonuclease) 2 300773 |
APEX2 database at LOVD
http://www.LOVD.nl/APEX2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
APLN
apelin 300297 |
APLN database at LOVD
http://www.LOVD.nl/APLN |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
APOO
apolipoprotein O 300753 |
APOO database at LOVD
http://www.LOVD.nl/APOO |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
APOOL
apolipoprotein O-like |
APOOL database at LOVD
http://www.LOVD.nl/APOOL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
APP
amyloid beta (A4) precursor protein 104760 |
Alzheimer Disease & Frontotemporal Dementia Mutation Database
http://www.molgen.ua.ac.be/ADMutations/ |
Marc Cruts Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
AQP1
aquaporin 1 (Colton blood group) 107776 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/projects/mhc/xslcgi.fcgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
AQP2
aquaporin 2 (collecting duct) 107777 |
Nephrogenic diabetes Insipidus
http://www.medicine.mcgill.ca/nephros/ |
Mary Fujiwara, Daniel G. Bichet McGill Uni.& Univ. de Montreal Montreal, Canada |
AQP9
aquaporin 9 602914 |
Aquaporin 9 (AQP9) database
http://lovd.bx.psu.edu/home.php?select_db=AQP9 |
Belinda Giardine and Joseph Borg |
AR
androgen receptor 313700 |
Androgen Receptor
http://androgendb.mcgill.ca/ |
Bruce Gottlieb L. Pinsky Lady Davis Inst. Med. Res., Montreal, Canada |
AR
androgen receptor 313700 |
AR database at LOVD
http://www.LOVD.nl/AR |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARAF
v-raf murine sarcoma 3611 viral oncogene homolog 311010 |
ARAF database at LOVD
http://www.LOVD.nl/ARAF |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARG1
arginase, liver 608313 |
ARG1database at LOVD
http://www.LOVD.nl/ARG1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARG2
arginase, type II 107830 |
Arginase, type II (ARG2) database
http://lovd.bx.psu.edu/home.php?select_db=ARG2 |
Belinda Giardine and Joseph Borg |
ARHGAP4
Rho GTPase activating protein 4 300023 |
ARHGAP4 database at LOVD
http://www.LOVD.nl/ARHGAP4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARHGAP6
Rho GTPase activating protein 6 300118 |
ARHGAP6 database at LOVD
http://www.LOVD.nl/ARHGAP6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARHGEF10
Rho guanine nucleotide exchange factor (GEF) 10 608136 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
ARHGEF6
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6 300267 |
ARHGEF6 database at LOVD
http://www.LOVD.nl/ARHGEF6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX1
armadillo repeat containing, X-linked 1 300362 |
ARMCX1 database at LOVD
http://www.LOVD.nl/ARMCX1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX2
armadillo repeat containing, X-linked 2 300363 |
ARMCX2 database at LOVD
http://www.LOVD.nl/ARMCX2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX3
armadillo repeat containing, X-linked 3 300364 |
ARMCX3 database at LOVD
http://www.LOVD.nl/ARMCX3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX4
armadillo repeat containing, X-linked 4 |
ARMCX4 database at LOVD
http://www.LOVD.nl/ARMCX4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX5
armadillo repeat containing, X-linked 5 |
ARMCX5 database at LOVD
http://www.LOVD.nl/ARMCX5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARMCX6
armadillo repeat containing, X-linked 6 |
ARMCX6 database at LOVD
http://www.LOVD.nl/ARMCX6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARSD
arylsulfatase D 300002 |
ARSD database at LOVD
http://www.LOVD.nl/ARSD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARSE
arylsulfatase E (chondrodysplasia punctata 1) 300180 |
ARSE database at LOVD
http://www.LOVD.nl/ARSE |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ARSF
arylsulfatase F 300003 |
ARSF database at LOVD
http://www.LOVD.nl/ARSF |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ART4
ADP-ribosyltransferase 4 (Dombrock blood group) 110600 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/projects/mhc/xslcgi.fcgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
ASB11
ankyrin repeat and SOCS box-containing 11 300626 |
ASB11 database at LOVD
http://www.LOVD.nl/ASB11 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASB12
ankyrin repeat and SOCS box-containing 12 |
ASB12 database at LOVD
http://www.LOVD.nl/ASB12 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASB9
ankyrin repeat and SOCS box-containing 9 |
ASB9 database at LOVD
http://www.LOVD.nl/ASB9 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASL
argininosuccinate lyase 608310 |
ASL database at LOVD
http://www.LOVD.nl/ASL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASMT
acetylserotonin O-methyltransferase 402500 |
ASMT database at LOVD
http://www.LOVD.nl/ASMT |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASMTL
acetylserotonin O-methyltransferase-like 400011 |
ASMTL database at LOVD
http://www.LOVD.nl/ASMTL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASPA
aspartoacylase (Canavan disease) 608034 |
aspartoacylase (Canavan disease) (ASPA) Variation Database
http://www.LOVD.nl/ASPA |
Gajja Salomons |
ASS1
argininosuccinate synthase 1 603470 |
ASS1 database at LOVD
http://www.LOVD.nl/ASS1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ASS1
argininosuccinate synthase 1 603470 |
Argininosuccinate synthetase 1 (ASS1) database
http://lovd.bx.psu.edu/home.php?select_db=ASS1 |
Belinda Giardine and Joseph Borg |
ATM
ataxia telangiectasia mutated 607585 |
ATM at LOVD
http://www.LOVD.nl/ATM |
Patrick Concannon, Memorial Sloan-Kettering Cancer Center, New York, USA |
ATP11C
ATPase, class VI, type 11C 300516 |
ATP11C database at LOVD
http://www.LOVD.nl/ATP11C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATP1A2
ATPase, Na+/K+ transporting, alpha 2 polypeptide 182340 |
ATP1A2 database at LOVD
http://www.LOVD.nl/ATP1A2 |
Boukje de Vries, LUMC, Leiden, The Netherlands |
ATP1B4
ATPase, Na+/K+ transporting, beta 4 polypeptide |
ATP1B4 database at LOVD
http://www.LOVD.nl/ATP1B4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATP2B3
ATPase, Ca++ transporting, plasma membrane 3 300014 |
ATP2B3 database at LOVD
http://www.LOVD.nl/ATP2B3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATP6AP2
ATPase, H+ transporting, lysosomal accessory protein 2 300556 |
ATP6AP2 database at LOVD
http://www.LOVD.nl/ATP6AP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATP7A
ATPase, Cu++ transporting, alpha polypeptide 300011 |
ATP7A database at LOVD
http://www.LOVD.nl/ATP7A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATP7B
ATPase, Cu++ transporting, beta polypeptide 606882 |
Wilson Disease Mutation Database
http://www.wilsondisease.med.ualberta.ca/database.asp |
Lisa Davies, Diane Cox, Dept Med Gen, Univ Alberta, Canada |
ATP7B
ATPase, Cu++ transporting, beta polypeptide 606882 |
The UMD ATP7B mutations database
http://www.umd.be/ATP7B/ |
Irene Ceballos, Paris, France |
ATP8B1
ATPase, aminophospholipid transporter, class I, type 8B, member 1 602397 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ATP8B1 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
ATRX
alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae) 300032 |
ATRX database at LOVD
http://www.LOVD.nl/ATRX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ATRX
alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae) 300032 |
alpha thalassemia/mental Retardation syndrome X-linked (ATRX) database
http://lovd.bx.psu.edu/home.php?select_db=ATRX |
Belinda Giardine and Joseph Borg |
ATXN3L
ataxin 3-like |
ATXN3L database at LOVD
http://www.LOVD.nl/ATXN3L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AUH
AU RNA binding protein/enoyl-CoA hydratase 600529 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=AUH |
Stefanie Kalb |
AVP
arginine vasopressin 192340 |
Nephrogenic diabetes Insipidus
http://www.medicine.mcgill.ca/nephros/ |
Mary Fujiwara, Daniel G. Bichet McGill Uni.& Univ. de Montreal Montreal, Canada |
AVP
arginine vasopressin 192340 |
nndi ARGININE VASOPRESSIN (AVP)
http://www.medgen.mcgill.ca/nndi/ |
NNDI Administrator and Ellen Buschman |
AVPR2
arginine vasopressin receptor 2 300538 |
Nephrogenic Diabetes Insipidus
http://www.medicine.mcgill.ca/nephros/ |
Mary Fujiwara, Daniel G. Bichet McGill Uni.& Univ. de Montreal Montreal, Canada |
AVPR2
arginine vasopressin receptor 2 300538 |
AVPR2 database at LOVD
http://www.LOVD.nl/AVPR2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AWAT1
acyl-CoA wax alcohol acyltransferase 1 |
AWAT1 database at LOVD
http://www.LOVD.nl/AWAT1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
AWAT2
acyl-CoA wax alcohol acyltransferase 2 |
AWAT2 database at LOVD
http://www.LOVD.nl/AWAT2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
B3GALTL
beta 1,3-galactosyltransferase-like 610308 |
B3GALTL - Peters' Plus syndrome at LOVD
http://www.LOVD.nl/B3GALTL |
Janneke Weiss, LUMC, Leiden, Nederland |
B4GALT1
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1 137060 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
BAG3
BCL2-associated athanogene 3 603883 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/BAG3 |
Johan T. den Dunnen Leiden Univ. Med Centre |
BBS1
Bardet-Biedl syndrome 1 209901 |
Mutations of the Bardet-Biedl Syndrome Type 1 Gene (BBS2L2)
http://www.retina-international.org/sci-news/bbs1mut.htm |
Retina International |
BBS2
Bardet-Biedl syndrome 2 606151 |
Mutations of the Bardet-Biedl Syndrome Type 2 Gene
http://www.retina-international.org/sci-news/bbs2mut.htm |
Retina International |
BBS4
Bardet-Biedl syndrome 4 600374 |
Mutations of the Bardet-Biedl Syndrome Type 4 Gene
http://www.retina-international.org/sci-news/bbs4mut.htm |
Retina International |
BBS7
Bardet-Biedl syndrome 7 607590 |
Mutations of the Bardet-Biedl Syndrome Type 7 Gene (BBS2L1)
http://www.retina-international.org/sci-news/bbs7mut.htm |
Retina International |
BCAM
basal cell adhesion molecule (Lutheran blood group) 111200 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/projects/mhc/xslcgi.fcgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
BCHE
butyrylcholinesterase 177400 |
ESTHER www server: ESTerases and alpha/beta Hydrolase Enzymes and Relatives
http://bioweb.ensam.inra.fr/ESTHER/general?what=index |
Xavier Cousin, Institut National de la Recherche, Agronomique, Montpellier, France |
BCL11A
B-cell CLL/lymphoma 11A (zinc finger protein) 606557 |
B-cell CLL/lymphoma 11A (BCL11A) database
http://lovd.bx.psu.edu/home.php?select_db=BCL11A |
Belinda Giardine and Joseph Borg |
BCOR
BCL6 co-repressor 300485 |
BCOR database at LOVD
http://www.LOVD.nl/BCOR |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BCORL1
BCL6 co-repressor-like 1 300688 |
BCORL1 database at LOVD
http://www.LOVD.nl/BCORL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BEND2
BEN domain containing 2 |
BEND2 database at LOVD
http://www.LOVD.nl/BEND2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BEST1
bestrophin 1 607854 |
University of Regensburg BEST1 database
http://www-huge.uni-regensburg.de/BEST1_database/home.php |
Heidi L. Schulz, Inst. of Human Genetics, University of Regensburg, Germany |
BEST1
bestrophin 1 607854 |
Mutations of the Bestrophin Gene
http://www.retina-international.org/sci-news/vmd2mut.htm |
Retina International |
BEX2
brain expressed X-linked 2 300691 |
BEX2 database at LOVD
http://www.LOVD.nl/BEX2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BEX4
brain expressed, X-linked 4 300692 |
BEX4 database at LOVD
http://www.LOVD.nl/BEX4 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BFSP1
beaded filament structural protein 1, filensin 603307 |
BFSP1 database at LOVD
http://www.LOVD.nl/BFSP1 |
Johan T. den Dunnen Leiden Univ. Med Centre |
BFSP2
beaded filament structural protein 2, phakinin 603212 |
Human Intermediate Filament Mutation Database
http://www.interfil.org/ |
W.H.I. McLean, Andrew Cassidy, Epithelial Genetics Group, Univ. Department of Human Genetics, Ninewells Hospital in Dundee, UK |
BFSP2
beaded filament structural protein 2, phakinin 603212 |
BFSP2 database at LOVD
http://www.LOVD.nl/BFSP2 |
Johan T. den Dunnen Leiden Univ. Med Centre |
BGN
biglycan 301870 |
BGN database at LOVD
http://www.LOVD.nl/BGN |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BHLHB9
basic helix-loop-helix domain containing, class B, 9 |
BHLHB9 database at LOVD
http://www.LOVD.nl/BHLHB9 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BIN1
bridging integrator 1 601248 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/BIN1 |
Johan T den Dunnen Leiden Univ. Med Centre |
BLM
Bloom syndrome, RecQ helicase-like 604610 |
BLMbase: Mutation registry for Bloom Syndrome
http://bioinf.uta.fi/BLMbase/index.php |
Mauno Vihinen, Univ. of Tampere, Finland |
BLNK
B-cell linker 604515 |
BLNKbase: Mutation registry for BLNK deficiency
http://bioinf.uta.fi/BLNKbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
BMP15
bone morphogenetic protein 15 300247 |
BMP15 database at LOVD
http://www.LOVD.nl/BMP15 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BMP2KL
BMP2 inducible kinase-like |
BMP2KL database at LOVD
http://www.LOVD.nl/BMP2KL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BMX
BMX non-receptor tyrosine kinase 300101 |
BMX database at LOVD
http://www.LOVD.nl/BMX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BRCA1
breast cancer 1, early onset 113705 |
Breast Cancer
http://research.nhgri.nih.gov/bic/ |
Lawrence C. Brody & Breast Cancer Information Core NCHGR/NIH Bethesda, U.S.A. |
BRCA1
breast cancer 1, early onset 113705 |
The UMD BRCA1 mutations database
http://www.umd.be/BRCA1/ |
R. Lidereau |
BRCA1
breast cancer 1, early onset 113705 |
Zhejiang University-Adinovo Center BRCA1 Database
http://www.china-hvp.org/LOVD/?select_db=BRCA1 |
Ming Qi, PhD, FACMG, Peikuan Cong and Min Pan |
BRCA1
breast cancer 1, early onset 113705 |
LOVD - BReast CAncer 1 - literature unclassified variants (BRCA1)
http://chromium.liacs.nl/LOVD2/cancer/home.php?select_db=BRCA1 |
Maaike Vreeswijk and Peter Devilee |
BRCA2
breast cancer 2, early onset 600185 |
Breast Cancer
http://research.nhgri.nih.gov/bic/ |
Lawrence C. Brody & Breast Cancer Information Core NCHGR/NIH Bethesda, U.S.A. |
BRCA2
breast cancer 2, early onset 600185 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen Auerbach, Rockefeller University, New York, USA |
BRCA2
breast cancer 2, early onset 600185 |
Zhejiang University-Adinovo Center BRCA2 Database
http://www.china-hvp.org/LOVD/?select_db=BRCA2 |
Ming Qi, PhD, FACMG, Peikuan Cong and Min Pan |
BRCA2
breast cancer 2, early onset 600185 |
LOVD - BReast CAncer 2 - literature unclassified variants (BRCA2)
http://chromium.liacs.nl/LOVD2/cancer/home.php?select_db=BRCA2 |
Maaike Vreeswijk and Peter Devilee |
BRIP1
BRCA1 interacting protein C-terminal helicase 1 605882 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
BRWD3
bromodomain and WD repeat domain containing 3 300553 |
BRWD3 database at LOVD
http://www.LOVD.nl/BRWD3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
BSCL2
Berardinelli-Seip congenital lipodystrophy 2 (seipin) 606158 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
BSG
basigin (Ok blood group) 109480 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
BTK
Bruton agammaglobulinemia tyrosine kinase 300300 |
BTK base: Mutation registry for X-linked agammaglobulinemia
http://bioinf.uta.fi/BTKbase/ |
Mauno Vihinen, C.I. Edvard Smith, Univ. of Tampere, Finland |
BTK
Bruton agammaglobulinemia tyrosine kinase 300300 |
BTK database at LOVD
http://www.LOVD.nl/BTK |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
C1GALT1C1
C1GALT1-specific chaperone 1 300611 |
C1GALT1C1 database at LOVD
http://www.LOVD.nl/C1GALT1C1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
C1QA
complement component 1, q subcomponent, A chain 120550 |
C1QAbase: Mutation registry for C1qA deficiency
http://bioinf.uta.fi/C1QAbase/index.php |
Mauno Vihinen, Univ. of Tampere, Finland |
C1QB
complement component 1, q subcomponent, B chain 120570 |
C1QBbase: Mutation registry for C1qB deficiency
http://bioinf.uta.fi/C1QBbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C1QC
complement component 1, q subcomponent, C chain 120575 |
C1QGbase: Mutation registry for C1qG deficiency
http://bioinf.uta.fi/C1QGbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C1S
complement component 1, s subcomponent 120580 |
C1Sbase: Mutation registry for C1s deficiency
http://bioinf.uta.fi/C1Sbase/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C2
complement component 2 217000 |
C2base: Mutation registry for C2 deficiency
http://bioinf.uta.fi/C2base/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C3
complement component 3 120700 |
C3base: Mutation registry for C3 deficiency
http://bioinf.uta.fi/C3base/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C5
complement component 5 120900 |
C5base: Mutation registry for C5 deficiency
http://bioinf.uta.fi/C5base/index2.html |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C6
complement component 6 217050 |
C6base: Mutation registry for C6 deficiency
http://bioinf.uta.fi/C6base/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C7
complement component 7 217070 |
C7base: Mutation registry for C7 deficiency
http://bioinf.uta.fi/C7base/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C8B
complement component 8, beta polypeptide 120960 |
C8Bbase: Mutation registry for C8B deficiency
http://bioinf.uta.fi/C8Bbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
C9
complement component 9 120940 |
C9base: Mutation registry for C9 deficiency
http://bioinf.uta.fi/C9base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CA2
carbonic anhydrase II 611492 |
CA2base: Mutation registry for Osteopetrosis with renal tubular acidosis
http://bioinf.uta.fi/CA2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CA5B
carbonic anhydrase VB, mitochondrial 300230 |
CA5B database at LOVD
http://www.LOVD.nl/CA5B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CACNA1A
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 601011 |
CAC1A1A database at LOVD
http://www.LOVD.nl/CACNA1A |
Elles Boon and Boukje de Vries, LUMC, Leiden, Nederland |
CACNA1A
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 601011 |
Familial Hemiplegic Migraine (FHM) Variation Database
http://grenada.lumc.nl/LOVD2/FHM/home.php?select_db=CACNA1A |
Paola Carrera PhD and Stefania Battistini MD PhD |
CACNA1C
calcium channel, voltage-dependent, L type, alpha 1C subunit 114205 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
CACNA1C
calcium channel, voltage-dependent, L type, alpha 1C subunit 114205 |
Zhejiang University-Adinovo Center CACNA1C Database
http://www.china-hvp.org/LOVD/?select_db=CACNA1C |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
CACNA1F
calcium channel, voltage-dependent, L type, alpha 1F subunit 300110 |
Mutations of the L-type Calcium-Channel Gene
http://www.retina-international.org/sci-news/cacnamut.htm |
Retina International |
CACNA1F
calcium channel, voltage-dependent, L type, alpha 1F subunit 300110 |
CACNA1F database at LOVD
http://www.LOVD.nl/CACNA1F |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CACNA1S
calcium channel, voltage-dependent, L type, alpha 1S subunit 114208 |
CACNA1S at LOVD
http://www.LOVD.nl/CACNA1S |
Ieke Ginjaar & Vincent Janmaat, LUMC, Leiden, Netherlands |
CAPN3
calpain 3, (p94) 114240 |
Calpain-3; Limb-Girdle Muscular Dystrophy, type 2A
http://www.LOVD.nl/CAPN3 |
Johan T. den Dunnen Leiden Univ. Med Centre,Leiden, The Netherlands |
CAPN6
calpain 6 300146 |
CAPN6 database at LOVD
http://www.LOVD.nl/CAPN6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CASK
calcium/calmodulin-dependent serine protein kinase (MAGUK family) 300172 |
CASK database at LOVD
http://www.LOVD.nl/CASK |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CASP10
caspase 10, apoptosis-related cysteine peptidase 601762 |
CASP10base: Mutation registry for Autoimmune lymphoproliferative syndrome, type II (ALPS2)
http://bioinf.uta.fi/CASP10base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CASP10
caspase 10, apoptosis-related cysteine peptidase 601762 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=CASP10 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
CASP8
caspase 8, apoptosis-related cysteine peptidase 601763 |
CASP8base: Mutation registry for Caspase 8 deficiency
http://bioinf.uta.fi/CASP8base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CASR
calcium-sensing receptor 601199 |
CASRdb Calcium Sensing Receptor Locus Mutation Database
http://www.casrdb.mcgill.ca |
Svetlana Pidasheva, Geoff Hendy, Manyphong Phommarinh, L.D'Souza-Li, McGill University Healt Centre Montreal, Canada |
CAV3
caveolin 3 601253 |
Limb-Girdle Muscular Dystrophy type 1C
http://www.LOVD.nl/CAV3 |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands |
CAV3
caveolin 3 601253 |
Zhejiang University-Adinovo Center CAV3 Database
http://www.china-hvp.org/LOVD/?select_db=CAV3 |
Ming Qi, PhD, FACMG, Peikuan Cong and Tao Zhang |
CBS
cystathionine-beta-synthase 236200 |
Cystathionine beta-synthase database
http://www.uchsc.edu/cbs/ |
Jan P. Kraus Univ. of Colorado Denver, U.S.A. |
CCDC120
coiled-coil domain containing 120 |
CCDC120 database at LOVD
http://www.LOVD.nl/CCDC120 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CCDC22
coiled-coil domain containing 22 |
CCDC22 database at LOVD
http://www.LOVD.nl/CCDC22 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CCNB3
cyclin B3 300456 |
CCNB3 database at LOVD
http://www.LOVD.nl/CCNB3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CD19
CD19 molecule 107265 |
CD19base: Mutation registry for CD19 deficiency
http://bioinf.uta.fi/CD19base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD247
CD247 molecule 186780 |
CD247base: Mutation registry for Autosomal recessive CD3Zeta deficiency
http://bioinf.uta.fi/CD247base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD3D
CD3d molecule, delta (CD3-TCR complex) 186790 |
CD3Dbase: Mutation registry for Autosomal recessive CD3delta deficiency
http://bioinf.uta.fi/CD3Dbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD3E
CD3e molecule, epsilon (CD3-TCR complex) 186830 |
CD3Ebase: Mutation registry for autosomal recessive CD3epsilon immunodeficiency
http://bioinf.uta.fi/CD3Ebase/ |
Mauno Vihinen, Jose R. Regueiro, Univ. of Tampere, Tampere, Finland |
CD3G
CD3g molecule, gamma (CD3-TCR complex) 186740 |
CD3Gbase: Mutation registry for autosomal recessive CD3gamma immunodeficiency
http://bioinf.uta.fi/CD3Gbase/ |
Mauno Vihinen, Jose R. Regueiro, Univ. of Tampere, Tampere, Finland |
CD40
CD40 molecule, TNF receptor superfamily member 5 109535 |
CD40base: Mutation registry for CD40 deficiency (previously known as TNFRSF5base)
http://bioinf.uta.fi/CD40base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD40LG
CD40 ligand 300386 |
CD40Lbase: Mutation registry for X-linked Hyper-IgM syndrome
http://bioinf.uta.fi/CD40Lbase/ |
Luigi D. Notarangelo, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD40LG
CD40 ligand 300386 |
Immunodeficiency with Increased IgM-The European CD40 Defect Database
http://www.expasy.ch/cd40lbase/cd40lbasestruct.html |
European Society for Immuno deficiencies |
CD40LG
CD40 ligand 300386 |
CD40LG database at LOVD
http://www.LOVD.nl/CD40LG |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CD40LG
CD40 ligand 300386 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=CD40LG |
Ammar Husami and Theru A. Sivakumaran |
CD55
CD55 molecule, decay accelerating factor for complement (Cromer blood group) 125240 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
CD55
CD55 molecule, decay accelerating factor for complement (Cromer blood group) 125240 |
CD55base: Mutation registry for Decay-accelerating factor (CD55) deficiency (previously known as DAFbase)
http://bioinf.uta.fi/CD55base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD59
CD59 molecule, complement regulatory protein 107271 |
CD59base: Mutation registry for CD59 deficiency
http://bioinf.uta.fi/CD59base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD79A
CD79a molecule, immunoglobulin-associated alpha 112205 |
CD79Abase: Mutation registry for Igα deficiency
http://bioinf.uta.fi/CD79Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD8A
CD8a molecule 186910 |
CD8Abase: Mutation registry for CD8 deficiency
http://bioinf.uta.fi/CD8Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CD99
CD99 molecule 450000 |
CD99 database at LOVD
http://www.LOVD.nl/CD99 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CD99L2
CD99 molecule-like 2 |
CD99L2 database at LOVD
http://www.LOVD.nl/CD99L2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CDH23
cadherin-related 23 605516 |
Hereditary Hearing Loss Homepage
http://hereditaryhearingloss.org/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
CDH23
cadherin-related 23 605516 |
Mutations of the Cadherin-related Protein 23 Gene
http://www.retina-international.org/sci-news/cdh23mut.htm |
Retina International |
CDH23
cadherin-related 23 605516 |
Retinal and hearing impairment genetic mutation database
http://www.LOVD.nl/CDH23 |
David Baux |
CDH23
cadherin-related 23 605516 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=CDH23 |
Ammar Husami and Theru A. Sivakumaran |
CDH3
cadherin 3, type 1, P-cadherin (placental) 114021 |
Mutations of the P-Cadherin Gene
http://www.retina-international.org/sci-news/cdh3mut.htm |
Retina International |
CDK16
cyclin-dependent kinase 16 311550 |
PCTK1 database at LOVD
http://www.LOVD.nl/CDK16 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CDKL5
cyclin-dependent kinase-like 5 300203 |
CDKL5 database at LOVD
http://www.LOVD.nl/CDKL5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CDKN2A
cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4) 600160 |
CDKN2a Database Project (a human p16 database with annotation)
https://biodesktop.uvm.edu/perl/p16 |
Marc Greenblatt Univ. of Vermont, Burlington VT, USA |
CDKN2A
cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4) 600160 |
CDKN2A database at LOVD
http://www.LOVD.nl/CDKN2A |
Janneke Weiss, LUMC, Leiden, The Netherlands |
CDR1
cerebellar degeneration-related protein 1, 34kDa 302650 |
CDR1 database at LOVD
http://www.LOVD.nl/CDR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CEBPE
CCAAT/enhancer binding protein (C/EBP), epsilon 600749 |
CEBPEbase: Mutation registry for Neutrophil-specific granule deficiency
http://bioinf.uta.fi/CEBPEbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CENPI
centromere protein I 300065 |
CENPI database at LOVD
http://www.LOVD.nl/CENPI |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CEP290
centrosomal protein 290kDa 610142 |
CEP290base
http://medgen.ugent.be/cep290base/ |
Frauke Coppieters Elfride De Baere |
CFD
complement factor D (adipsin) 134350 |
CFDbase: Mutation registry for Factor D deficiency (previously known as DFbase)
http://bioinf.uta.fi/CFDbase/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CFH
complement factor H 134370 |
CFHbase: Mutation registry for Factor H deficiency (previously known as HF1base)
http://bioinf.uta.fi/CFHbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CFI
complement factor I 217030 |
CFIbase: Mutation registry for Factor I deficiency (previously known as IFbase)
http://bioinf.uta.fi/CFIbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CFL2
cofilin 2 (muscle) 601443 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/CFL2 |
Johan T. den Dunnen Leiden Univ. Med Centre |
CFP
complement factor properdin 300383 |
PFCbase: Mutation registry for properdin deficiency
http://bioinf.uta.fi/PFCbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CFP
complement factor properdin 300383 |
CFP database at LOVD
http://www.LOVD.nl/CFP |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CFTR
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) 602421 |
Cystic Fibrosis
http://www.genet.sickkids.on.ca/cftr/ |
Lap Chee Tsui The Hospital for Sick Children, Toronto, Canada |
CHM
choroideremia (Rab escort protein 1) 300390 |
Mutations of the Rab Escort Protein 1
http://www.retina-international.org/sci-news/repmut.htm |
Retina International |
CHM
choroideremia (Rab escort protein 1) 300390 |
CHM database at LOVD
http://www.LOVD.nl/CHM |
D. Baux, Institut Universitaire de Recherche Clinique UFR M�decine Site NORD, Montpellier, France |
CHMP4B
chromatin modifying protein 4B 610897 |
CHMP4B database at LOVD
http://www.LOVD.nl/CHMP4B |
Johan T den Dunnen Leiden Univ. Med Centre |
CHRDL1
chordin-like 1 300350 |
CHRDL1 database at LOVD
http://www.LOVD.nl/CHRDL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CHRNG
cholinergic receptor, nicotinic, gamma 100730 |
Cholinergic receptor, nicotinic, gamma polypeptide (CHRNG) variation database
http://www.LOVD.nl/CHRNG |
Dr Julie Vogt and Dr Derek Lim |
CIITA
class II, major histocompatibility complex, transactivator 600005 |
CIITAbase: Mutation registry for MHCII transactivating protein deficiency (previously known as MHC2TAbase)
http://bioinf.uta.fi/CIITAbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CITED1
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1 300149 |
CITED1 database at LOVD
http://www.LOVD.nl/CITED1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CLCN1
chloride channel 1, skeletal muscle 118425 |
CLCN1 - Chloride channel 1, skeletal muscle
http://www.LOVD.nl/CLCN1 |
Ieke Ginjaar and Vincent Janmaat, Clinical Genetics, LUMC, Leiden |
CLCN4
chloride channel 4 302910 |
CLCN4 database at LOVD
http://www.LOVD.nl/CLCN4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CLCN5
chloride channel 5 300008 |
CLCN5 database at LOVD
http://www.LOVD.nl/CLCN5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CLCN7
chloride channel 7 602727 |
CLCN7base: Mutation registry for Autosomal dominant osteopetrosis, type 2
http://bioinf.uta.fi/CLCN7base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CLDN14
claudin 14 605608 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
CLDN2
claudin 2 300520 |
CLDN2 database at LOVD
http://www.LOVD.nl/CLDN2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CLIC2
chloride intracellular channel 2 300138 |
CLIC2 database at LOVD
http://www.LOVD.nl/CLIC2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CLN3
ceroid-lipofuscinosis, neuronal 3 607042 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
CLN3
ceroid-lipofuscinosis, neuronal 3 607042 |
Mutations of the CLN3 Gene
http://www.retina-international.org/sci-news/cln3mut.htm |
Retina International |
CLN4
ceroid-lipofuscinosis, neuronal 4 (Kufs disease) 204300 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
CLN5
ceroid-lipofuscinosis, neuronal 5 608102 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
CLN6
ceroid-lipofuscinosis, neuronal 6, late infantile, variant 606725 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
CLN8
ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) 607837 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
CLRN1
clarin 1 606397 |
Mutations of the Usher Syndrome Type 3 Gene (USH3)
http://www.retina-international.org/sci-news/ush3mut.htm |
Retina International |
CLRN1
clarin 1 606397 |
The UMD USH3A mutations database
http://www.umd.be/USH3A/ |
A.-F. Roux and D. Baux |
CLRN1
clarin 1 606397 |
Retinal and hearing impairment genetic mutation database
https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CLRN1 |
David Baux |
CLRN1
clarin 1 606397 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=CLRN1 |
Ammar Husami and Theru A. Sivakumaran |
CNGA1
cyclic nucleotide gated channel alpha 1 123825 |
Mutations of the Cyclic Nucleotide-gated Cation Channel
http://www.retina-international.org/sci-news/cnga1mut.htm |
Retina International |
CNGA2
cyclic nucleotide gated channel alpha 2 300338 |
CNGA2 database at LOVD
http://www.LOVD.nl/CNGA2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CNGA3
cyclic nucleotide gated channel alpha 3 600053 |
Mutations of the Cone Cyclic Nucleotide-gated Cation Channel
http://www.retina-international.org/sci-news/cnga3mut.htm |
Retina International |
CNKSR2
connector enhancer of kinase suppressor of Ras 2 300724 |
CNKSR2 database at LOVD
http://www.LOVD.nl/CNKSR2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CNTN1
contactin 1 600016 |
CNTN1 - Leiden Muscular Dystrophy pages
http://www.LOVD.nl/CNTN1 |
Johan T den Dunnen Leiden Univ. Med Centre |
CNTNAP2
contactin associated protein-like 2 604569 |
Contactin associated protein-like 2 (CNTNAP2) database
http://lovd.bx.psu.edu/home.php?select_db=CNTNAP2 |
Belinda Giardine and Joseph Borg |
COCH
coagulation factor C homolog, cochlin (Limulus polyphemus) 603196 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
COL11A2
collagen, type XI, alpha 2 120290 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
COL1A1
collagen, type I, alpha 1 120150 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
COL1A2
collagen, type I, alpha 2 120160 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
COL3A1
collagen, type III, alpha 1 120180 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
COL3A1
collagen, type III, alpha 1 120180 |
The UMD COL3A1 mutations database
http://www.umd.be/COL3A1/ |
P. Khau van Kien |
COL4A5
collagen, type IV, alpha 5 303630 |
ALPORT syndrome and COL4A5 gene Database
http://www.arup.utah.edu/database/ALPORT/ALPORT_welcome.php |
Genevieve Pont-Kingdon, PhD, ARUP Institute for Clinical and Experimental Pathology(r), Salt Lake City, UT, USA |
COL4A5
collagen, type IV, alpha 5 303630 |
Collagen, type IV, alpha 5 (COL4A5) Mental Retardation Database
http://www.LOVD.nl/COL4A5 |
Judy Savige |
COL4A6
collagen, type IV, alpha 6 303631 |
Collagen, type IV, alpha 6 (COL4A6) Mental Retardation Database
http://www.LOVD.nl/COL4A6 |
Judy Savige |
COL5A1
collagen, type V, alpha 1 120215 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
COL5A2
collagen, type V, alpha 2 120190 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
COL6A1
collagen, type VI, alpha 1 120220 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/COL6A1 |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands and Anne Lampe, University Newcastle upon Tyne, UK |
COL6A2
collagen, type VI, alpha 2 120240 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/COL6A2 |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands and Anne Lampe, University Newcastle upon Tyne, UK |
COL6A3
collagen, type VI, alpha 3 120250 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/COL6A3 |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands and Anne Lampe, University Newcastle upon Tyne, UK |
COL7A1
collagen, type VII, alpha 1 120120 |
Medical Genetics Department Institute of Mother and Child
http://www.col7.info |
Prof. Cezary Kowalewski, Katarzyna Wertheim-Tysarowska, |
COLQ
collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase 603033 |
ESTHER www server: ESTerases and alpha/beta Hydrolase Enzymes & Relatives
http://bioweb.ensam.inra.fr/ESTHER/general?what=index |
Xavier Cousin, Institut National de la Recherche, Agronomique, Montpellier, France |
CPS1
carbamoyl-phosphate synthetase 1, mitochondrial 608307 |
CPS1 database at LOVD
http://www.LOVD.nl/CPS1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CPXCR1
CPX chromosome region, candidate 1 |
CPXCR1 database at LOVD
http://www.LOVD.nl/CPXCR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CR1
complement component (3b/4b) receptor 1 (Knops blood group) 120620 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
CRB1
crumbs homolog 1 (Drosophila) 604210 |
Mutations of the Human Crumbs Homologue 1
http://www.retina-international.org/sci-news/crb1mut.htm |
Retina International |
CREBBP
CREB binding protein 600140 |
CREBBP - Rubinstein-Taybi Syndrome (RSTS)
http://www.LOVD.nl/CREBBP |
Dorien Peters, Clinical Genetics, LUMC, Leiden |
CRTAP
cartilage associated protein 605497 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
CRX
cone-rod homeobox 602225 |
Mutations of the Cone Rod Homeobox Gene
http://www.retina-international.org/sci-news/crxmut.htm |
Retina International |
CRYAA
crystallin, alpha A 123580 |
CRYAA database at LOVD
http://www.LOVD.nl/CRYAA |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYAB
crystallin, alpha B 123590 |
CRYAB database at LOVD
http://www.LOVD.nl/CRYAB |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYBA1
crystallin, beta A1 123610 |
CRYBA1 database at LOVD
http://www.LOVD.nl/CRYBA1 |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYBA4
crystallin, beta A4 123631 |
CRYBA4 database at LOVD
http://www.LOVD.nl/CRYBA4 |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYBB1
crystallin, beta B1 600929 |
CRYBB1 database at LOVD
http://www.LOVD.nl/CRYBB1 |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYBB2
crystallin, beta B2 123620 |
CRYBB2 database at LOVD
http://www.LOVD.nl/CRYBB2 |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYBB3
crystallin, beta B3 123630 |
CRYBB3 database at LOVD
http://www.LOVD.nl/CRYBB3 |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYGC
crystallin, gamma C 123680 |
CRYGC database at LOVD
http://www.LOVD.nl/CRYGC |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYGD
crystallin, gamma D 123690 |
CRYGD database at LOVD
http://www.LOVD.nl/CRYGD |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYGS
crystallin, gamma S 123730 |
CRYGS database at LOVD
http://www.LOVD.nl/CRYGS |
Lars Hansen Institute of Cellular and Molecular Medicine, Section IV, The Panum Institute. University of Copenhagen, Copenhagen, Denmark |
CRYM
crystallin, mu 123740 |
CRYM database at LOVD
http://www.LOVD.nl/CRYM |
Johan T den Dunnen Leiden Univ. Med Centre |
CSAG1
chondrosarcoma associated gene 1 |
CSAG1 database at LOVD
http://www.LOVD.nl/CSAG1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CSAG4
CSAG family, member 4 |
CSAG4 database at LOVD
http://grenada.lumc.nl/LOVD2/MR/home.php?select_db=CSAG4 |
Ing. Ivo F.A.C. Fokkema |
CSF2RA
colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage) 425000 |
CSF2RA database at LOVD
http://www.LOVD.nl/CSF2RA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CSNK2A1
casein kinase 2, alpha 1 polypeptide 115440 |
Casein kinase 2, alpha 1 polypeptide (CSNK2A1) database
http://lovd.bx.psu.edu/home.php?select_db=CSNK2A1 |
Belinda Giardine and Joseph Borg |
CSTF2
cleavage stimulation factor, 3' pre-RNA, subunit 2, 64kDa 600368 |
CSTF2 database at LOVD
http://www.LOVD.nl/CSTF2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CT45A2
cancer/testis antigen family 45, member A2 300793 |
CT45A2 database at LOVD
http://www.LOVD.nl/CT45A2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CT45A5
cancer/testis antigen family 45, member A5 300796 |
CT45A5 database at LOVD
http://www.LOVD.nl/CT45A5 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CTAG2
cancer/testis antigen 2 300396 |
CTAG2 database at LOVD
http://www.LOVD.nl/CTAG2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CTDP1
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 604927 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
CTPS2
CTP synthase II 300380 |
CTPS2 database at LOVD
http://www.LOVD.nl/CTPS2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CTSC
cathepsin C 602365 |
CTSCbase: Mutation registry for Papillon-Lefevre syndrome
http://bioinf.uta.fi/CTSCbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CTSK
cathepsin K 601105 |
Cathepsin K Mutations DataBase
http://www.fmmukq.com/boke1/showxswz.jsp?wbtreeid=1084&articleid=1075&doctorid=1201 |
Xiaohong Duan, Yang Xue |
CUL4B
cullin 4B 300304 |
CUL4B database at LOVD
http://www.LOVD.nl/CUL4B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXCR4
chemokine (C-X-C motif) receptor 4 162643 |
CXCR4base: Mutation registry for WHIM syndrome (warts, hypogammaglobulinemia, immunodeficiency, and myelokathexis)
http://bioinf.uta.fi/CXCR4base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CXorf1
chromosome X open reading frame 1 300565 |
CXorf1 database at LOVD
http://www.LOVD.nl/CXorf1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf21
chromosome X open reading frame 21 |
CXorf21 database at LOVD
http://www.LOVD.nl/CXorf21 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf22
chromosome X open reading frame 22 |
CXorf22 database at LOVD
http://www.LOVD.nl/CXorf22 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf23
chromosome X open reading frame 23 |
CXorf23 database at LOVD
http://www.LOVD.nl/CXorf23 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf24
chromosome X open reading frame 24 |
CXorf24 database at LOVD
http://www.LOVD.nl/CXorf24 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf27
chromosome X open reading frame 27 |
CXorf27 database at LOVD
http://www.LOVD.nl/CXorf27 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf28
chromosome X open reading frame 28 |
CXorf28 database at LOVD
http://www.LOVD.nl/CXorf28 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf30
chromosome X open reading frame 30 |
CXorf30 database at LOVD
http://www.LOVD.nl/CXorf30 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf36
chromosome X open reading frame 36 |
CXorf36 database at LOVD
http://www.LOVD.nl/CXorf36 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf38
chromosome X open reading frame 38 |
CXorf38 database at LOVD
http://www.LOVD.nl/CXorf38 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf41
chromosome X open reading frame 41 |
CXorf41 database at LOVD
http://www.LOVD.nl/CXorf41 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf56
chromosome X open reading frame 56 |
CXorf56 database at LOVD
http://www.LOVD.nl/CXorf56 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf57
chromosome X open reading frame 57 |
CXorf57 database at LOVD
http://www.LOVD.nl/CXorf57 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf58
chromosome X open reading frame 58 |
CXorf58 database at LOVD
http://www.LOVD.nl/CXorf58 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf59
chromosome X open reading frame 59 |
CXorf59 database at LOVD
http://www.LOVD.nl/CXorf59 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf64
chromosome X open reading frame 64 |
CXorf64 database at LOVD
http://www.LOVD.nl/CXorf64 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf65
chromosome X open reading frame 65 |
CXorf65 database at LOVD
http://www.LOVD.nl/CXorf65 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CXorf66
chromosome X open reading frame 66 |
CXorf66 database at LOVD
http://www.LOVD.nl/CXorf66 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
CYBA
cytochrome b-245, alpha polypeptide 608508 |
CYBAbase: Mutation registry for autosomal recessive chronic granulomatous disease (CGD), deficiency of p22phox
http://bioinf.uta.fi/CYBAbase/ |
Dirk Roos, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CYBB
cytochrome b-245, beta polypeptide 300481 |
CYBBbase: Mutation registry for X-linked chronic granulomatous disease (previously known as X-CDGbase)
http://bioinf.uta.fi/CYBBbase/ |
Dirk Roos, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
CYP19A1
cytochrome P450, family 19, subfamily A, polypeptide 1 107910 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP1A1
cytochrome P450, family 1, subfamily A, polypeptide 1 108330 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP1A2
cytochrome P450, family 1, subfamily A, polypeptide 2 124060 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP1B1
cytochrome P450, family 1, subfamily B, polypeptide 1 601771 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingeman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP21A2
cytochrome P450, family 21, subfamily A, polypeptide 2 201910 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP26A1
cytochrome P450, family 26, subfamily A, polypeptide 1 602239 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP27A1
cytochrome P450, family 27, subfamily A, polypeptide 1 606530 |
Cerebrotendinous Xanthomatosis
http://www.LOVD.nl/CYP27A1 |
Jorge Amigo Lechuga and Mar�a Jes�s Sobrido |
CYP2A13
cytochrome P450, family 2, subfamily A, polypeptide 13 608055 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2A6
cytochrome P450, family 2, subfamily A, polypeptide 6 122720 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2B6
cytochrome P450, family 2, subfamily B, polypeptide 6 123930 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2C19
cytochrome P450, family 2, subfamily C, polypeptide 19 124020 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2C8
cytochrome P450, family 2, subfamily C, polypeptide 8 601129 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2C9
cytochrome P450, family 2, subfamily C, polypeptide 9 601130 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2D6
cytochrome P450, family 2, subfamily D, polypeptide 6 124030 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2E1
cytochrome P450, family 2, subfamily E, polypeptide 1 124040 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2F1
cytochrome P450, family 2, subfamily F, polypeptide 1 124070 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2J2
cytochrome P450, family 2, subfamily J, polypeptide 2 601258 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2R1
cytochrome P450, family 2, subfamily R, polypeptide 1 608713 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2S1
cytochrome P450, family 2, subfamily S, polypeptide 1 611529 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP2W1
cytochrome P450, family 2, subfamily W, polypeptide 1 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP3A4
cytochrome P450, family 3, subfamily A, polypeptide 4 124010 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP3A43
cytochrome P450, family 3, subfamily A, polypeptide 43 606534 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP3A5
cytochrome P450, family 3, subfamily A, polypeptide 5 605325 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP3A7
cytochrome P450, family 3, subfamily A, polypeptide 7 605340 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP4A11
cytochrome P450, family 4, subfamily A, polypeptide 11 601310 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP4A22
cytochrome P450, family 4, subfamily A, polypeptide 22 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP4B1
cytochrome P450, family 4, subfamily B, polypeptide 1 124075 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYP4F2
cytochrome P450, family 4, subfamily F, polypeptide 2 604426 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
CYSLTR1
cysteinyl leukotriene receptor 1 300201 |
CYSLTR1 database at LOVD
http://www.LOVD.nl/CYSLTR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
D2HGDH
D-2-hydroxyglutarate dehydrogenase 609186 |
D2HGDH database at LOVD
http://www.LOVD.nl/D2HGDH |
Gajja Salomons |
DACH2
dachshund homolog 2 (Drosophila) 300608 |
DACH2 database at LOVD
http://www.LOVD.nl/DACH2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DAG1
dystroglycan 1 (dystrophin-associated glycoprotein 1) 128239 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/DAG1 |
JT den Dunnen |
DARC
Duffy blood group, chemokine receptor 110700 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
DBH
dopamine beta-hydroxylase (dopamine beta-monooxygenase) 609312 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
DCAF12L1
DDB1 and CUL4 associated factor 12-like 1 |
DCAF12L1 database at LOVD
http://www.LOVD.nl/DCAF12L1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DCAF12L2
DDB1 and CUL4 associated factor 12-like 2 |
DCAF12L2 database at LOVD
http://www.LOVD.nl/DCAF12L2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DCAF8L1
DDB1 and CUL4 associated factor 8-like 1 |
DCAF8L1 database at LOVD
http://www.LOVD.nl/DCAF8L1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DCLRE1C
DNA cross-link repair 1C (PSO2 homolog, S. cerevisiae) 605988 |
DCLRE1Cbase: Mutation registry for Artemis deficiency
http://bioinf.uta.fi/DCLRE1Cbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
DCTN1
dynactin 1 (p150, glued homolog, Drosophila) 601143 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
DDC
dopa decarboxylase (aromatic L-amino acid decarboxylase) 107930 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
DDX3X
DEAD (Asp-Glu-Ala-Asp) box polypeptide 3, X-linked 300160 |
DDX3X database at LOVD
http://www.LOVD.nl/DDX3X |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DDX53
DEAD (Asp-Glu-Ala-Asp) box polypeptide 53 |
DDX53 database at LOVD
http://www.LOVD.nl/DDX53 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DES
desmin 125660 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/DES |
Johan den Dunnen, LUMC, Leiden, Nederland |
DFNA5
deafness, autosomal dominant 5 608798 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
DFNB31
deafness, autosomal recessive 31 607928 |
Retinal and hearing impairment genetic mutation database WHRN
http://www.LOVD.nl/WHRN |
David Baux |
DFNB31
deafness, autosomal recessive 31 607928 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=DFNB31 |
Ammar Husami and Theru A. Sivakumaran |
DHCR7
7-dehydrocholesterol reductase 602858 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=DHCR7 |
Martina Witsch-Baumgartner |
DIAPH1
diaphanous homolog 1 (Drosophila) 602121 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
DIAPH2
diaphanous homolog 2 (Drosophila) 300108 |
DIAPH2 database at LOVD
http://www.LOVD.nl/DIAPH2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DKC1
dyskeratosis congenita 1, dyskerin 300126 |
DKC1base: Mutation registry for Hoyeraal-Hreidarsson syndrome
http://bioinf.uta.fi/DKC1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
DKC1
dyskeratosis congenita 1, dyskerin 300126 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#dkc1 |
Julian J-L Chen at Arizona State University |
DKC1
dyskeratosis congenita 1, dyskerin 300126 |
DKC1 database at LOVD
http://www.LOVD.nl/DKC1 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy � |
DLG3
discs, large homolog 3 (Drosophila) 300189 |
DLG3 database at LOVD
http://www.LOVD.nl/DLG3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DMD
dystrophin 300377 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/DMD |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
DMD
dystrophin 300377 |
The DMD mutations database UMD-DMD France
http://www.umd.be/DMD/W_DMD/index.html |
France Leturcq - H�pital Cochin, Paris and Sylvie Tuffery-Giraud - Universit� Montpellier 1 |
DMD
dystrophin 300377 |
Duchenne Muscular Dystrophy pages (whole exon changes)
http://www.LOVD.nl/DMD_d |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
DNASE1L1
deoxyribonuclease I-like 1 300081 |
DNASE1L1 database at LOVD
http://www.LOVD.nl/DNASE1L1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DNM2
dynamin 2 602378 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
DNM2
dynamin 2 602378 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/DNM2 |
Johan T den Dunnen Leiden Univ. Med Centre |
DNMT3B
DNA (cytosine-5-)-methyltransferase 3 beta 602900 |
DNMT3Bbase: Mutation registry for ICF syndrome
http://bioinf.uta.fi/DNMT3Bbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
DOK7
docking protein 7 610285 |
DOK7 - Leiden Muscular Dystrophy pages
http://www.LOVD.nl/DOK7 |
Tom Winder |
DPAGT1
dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase) 191350 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
DPM1
dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit 603503 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs Center for Human Genetics Leuven, Belgium |
DPM3
dolichyl-phosphate mannosyltransferase polypeptide 3 605951 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/DPM3 |
Johan T den Dunnen Leiden Univ. Med Centre |
DPYD
dihydropyrimidine dehydrogenase 274270 |
UMD Locus Specific Databases
http://www.umd.be/DPYD/ |
Jean Christophe Boyer, Nimes, France |
DRP2
dystrophin related protein 2 300052 |
DRP2 database at LOVD
http://www.LOVD.nl/DRP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DSC2
desmocollin 2 125645 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
DSG2
desmoglein 2 125671 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
DSP
desmoplakin 125647 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
DTNA
dystrobrevin, alpha 601239 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/DTNA |
Johan T. den Dunnen, Leiden Univ.Med Centre, Leiden, The Netherlands |
DUSP21
dual specificity phosphatase 21 300678 |
DUSP21 database at LOVD
http://www.LOVD.nl/DUSP21 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DYNLT3
dynein, light chain, Tctex-type 3 300302 |
DYNLT3 database at LOVD
http://www.LOVD.nl/DYNLT3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
DYSF
dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) 603009 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/DYSF |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands |
Go Back To Main Index! | ||
EDA
ectodysplasin A 300451 |
EDA database at LOVD
http://www.LOVD.nl/EDA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EDA2R
ectodysplasin A2 receptor 300276 |
EDA2R database at LOVD
http://www.LOVD.nl/EDA2R |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EDN3
endothelin 3 131242 |
EDN3 database at LOVD
http://www.LOVD.nl/EDN3 |
Veronique Pingault Laboratoire de Biochimie et G�n�tique, Hopital Henri Mondor Creteil cedex, France |
EDNRB
endothelin receptor type B 131244 |
EDNRB database at LOVD
http://grenada.lumc.nl/LOVD2/WS/home.php?select_db=EDNRB |
Veronique Pingault Laboratoire de Biochimie et G�n�tique, Hopital Henri Mondor Creteil cedex, France |
EFEMP1
EGF-containing fibulin-like extracellular matrix protein 1 601548 |
Mutations of the EGF-containing fibulin-like extracellular matrix protein 1
http://www.retina-international.org/sci-news/efempmut.htm |
Retina International |
EFHC2
EF-hand domain (C-terminal) containing 2 |
EFHC2 database at LOVD
http://www.LOVD.nl/EFHC2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EFNB1
ephrin-B1 300035 |
EFNB1 database at LOVD
http://www.LOVD.nl/EFNB1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EGFL6
EGF-like-domain, multiple 6 300239 |
EGFL6 database at LOVD
http://www.LOVD.nl/EGFL6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EGR2
early growth response 2 129010 |
Mutation Database of Inherited Peripheral Neuropathies
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
EIF2S3
eukaryotic translation initiation factor 2, subunit 3 gamma, 52kDa 300161 |
EIF2S3 database at LOVD
http://www.LOVD.nl/EIF2S3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ELANE
elastase, neutrophil expressed 130130 |
ELA2base: Mutation registry for Cyclic and congenital neutropenia
http://bioinf.uta.fi/ELA2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
ELANE
elastase, neutrophil expressed 130130 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=ELANE |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
ELF4
E74-like factor 4 (ets domain transcription factor) 300775 |
ELF4 database at LOVD
http://www.LOVD.nl/ELF4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ELK1
ELK1, member of ETS oncogene family 311040 |
ELK1 database at LOVD
http://www.LOVD.nl/ELK1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ELOVL4
elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 605512 |
Mutations of the Elongation of Very Long Chain Fatty Acids-like Protein 4 Gene
http://www.retina-international.org/sci-news/elovlmut.htm |
Retina International |
EMD
emerin 300384 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/EMD |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
EMD
emerin 300384 |
The UMD EMD mutations database
http://www.umd.be/EMD/ |
G. Bonne, France |
ENG
endoglin 131195 |
Hereditary Hemorrhagic Telangiectasia (HHT) Mutation Database
http://www.macs.hw.ac.uk/hht/ |
Paul Westwood, The Molecular Genetics Service, Edinburgh, UK |
ENOX2
ecto-NOX disulfide-thiol exchanger 2 300282 |
ENOX2 database at LOVD
http://www.LOVD.nl/ENOX2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EP300
E1A binding protein p300 602700 |
EP300 - Rubinstein-Taybi Syndrome (RSTS)
http://www.LOVD.nl/EP300 |
Dorien Peters, Clinical Genetics, LUMC, Leiden |
EPCAM
epithelial cell adhesion molecule 185535 |
InSiGHT - EPCAM
http://www.LOVD.nl/EPCAM |
Michael Woods, Amanda Dohey and Johan den Dunnen |
ERCC2
excision repair cross-complementing rodent repair deficiency, complementation group 2 126340 |
Excision repair cross-complementing rodent repair deficiency, complementati (ERCC2) database
http://lovd.bx.psu.edu/home.php?select_db=ERCC2 |
Belinda Giardine and Joseph Borg |
ERMAP
erythroblast membrane-associated protein (Scianna blood group) 609017 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Department of Biochemistry, Santosh Patnaik, Department of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
ESCO2
establishment of cohesion 1 homolog 2 (S. cerevisiae) 609353 |
ESCO2 database at LOVD
http://www.LOVD.nl/ESCO2 |
Birgitt Schuele, USA |
ESX1
ESX homeobox 1 300154 |
ESX1 database at LOVD
http://www.LOVD.nl/ESX1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
EXT1
exostoses (multiple) 1 608177 |
Multiple Osteochondroma Mutation Database
http://medgen.ua.ac.be/LOVDv.2.0/home.php?select_db=EXT1 |
Database Administrators |
EXT2
exostoses (multiple) 2 608210 |
Multiple Osteochondroma Mutation Database
http://medgen.ua.ac.be/LOVDv.2.0/home.php?select_db=EXT2 |
Database Administrators |
EYA4
eyes absent homolog 4 (Drosophila) 603550 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
Go Back To Main Index! | ||
F12
coagulation factor XII (Hageman factor) 610619 |
F12base: Mutation registry for Hereditary angioedema type III
http://bioinf.uta.fi/F12base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
F8
coagulation factor VIII, procoagulant component 306700 |
The Haemophilia A Mutation, Structure, Test & Resource Site (HAMSTeRS)
http://hadb.org.uk/ |
Dr Geoffrey Kemball-Cook |
F8
coagulation factor VIII, procoagulant component 306700 |
F8 database at LOVD
http://www.LOVD.nl/F8 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
F8
coagulation factor VIII, procoagulant component 306700 |
F8 Mutation Registry at Hemobase
http://www.hemobase.com/en/Base_de_datos_HA.htm |
Francisco Vidal, Lorena Ramirez |
F9
coagulation factor IX 300746 |
Haemophilia B Mutation Database
http://www.kcl.ac.uk/ip/petergreen/haemBdatabase.html |
P.M Green, F. Giannelli Division of Genetics & Development 7th Floor Guys Tower, GKT School of Medicine, Guy's Hospital London SE1 9RT United Kingdom and consortium |
F9
coagulation factor IX 300746 |
F9 database at LOVD
http://www.LOVD.nl/F9 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
F9
coagulation factor IX 300746 |
F9 Mutation Registry at Hemobase
http://www.hemobase.com/en/Base_de_datos_HB.htm |
Francisco Vidal, Lorena Ramirez |
FAAH2
fatty acid amide hydrolase 2 300654 |
FAAH2 database at LOVD
http://www.LOVD.nl/FAAH2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM120C
family with sequence similarity 120C 300741 |
FAM120C database at LOVD
http://www.LOVD.nl/FAM120C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM122B
family with sequence similarity 122B |
FAM122B database at LOVD
http://www.LOVD.nl/FAM122B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM122C
family with sequence similarity 122C |
FAM122C database at LOVD
http://www.LOVD.nl/FAM122C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM123B
family with sequence similarity 123B 300647 |
FAM123B database at LOVD
http://www.LOVD.nl/FAM123B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM133A
family with sequence similarity 133, member A |
FAM133A database at LOVD
http://www.LOVD.nl/FAM133A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM155B
family with sequence similarity 155, member B |
FAM155B database at LOVD
http://www.LOVD.nl/FAM155B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM3A
family with sequence similarity 3, member A 300492 |
FAM3A database at LOVD
http://www.LOVD.nl/FAM3A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM45B
family with sequence similarity 45, member B |
FAM45B database at LOVD
http://www.LOVD.nl/FAM45B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM46D
family with sequence similarity 46, member D |
FAM46D database at LOVD
http://www.LOVD.nl/FAM46D |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM47A
family with sequence similarity 47, member A |
FAM47A database at LOVD
http://www.LOVD.nl/FAM47A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM47B
family with sequence similarity 47, member B |
FAM47B database at LOVD
http://www.LOVD.nl/FAM47B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM47C
family with sequence similarity 47, member C |
FAM47C database at LOVD
http://www.LOVD.nl/FAM47C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM50A
family with sequence similarity 50, member A 300453 |
FAM50A database at LOVD
http://www.LOVD.nl/FAM50A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM9A
family with sequence similarity 9, member A 300477 |
FAM9A database at LOVD
http://www.LOVD.nl/FAM9A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FAM9C
family with sequence similarity 9, member C 300479 |
FAM9C database at LOVD
http://www.LOVD.nl/FAM9C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FANCA
Fanconi anemia, complementation group A 607139 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCB
Fanconi anemia, complementation group B 300515 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCC
Fanconi anemia, complementation group C 227645 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCD2
Fanconi anemia, complementation group D2 227646 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCE
Fanconi anemia, complementation group E 600901 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCF
Fanconi anemia, complementation group F 603467 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCG
Fanconi anemia, complementation group G 602956 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCI
Fanconi anemia, complementation group I 611360 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCL
Fanconi anemia, complementation group L 608111 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen D. Auerbach, PhD The Rockefeller University, NY Detlev Schindler,MD,PhD University of Wuerzburg, Germany and consortium |
FANCM
Fanconi anemia, complementation group M 609644 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen Auerbach, Rockefeller University, New York, USA |
FAS
Fas (TNF receptor superfamily, member 6) 134637 |
Autoimmune Lymphoproliferative Syndrome Database (ALPSbase): Database of mutations causing human ALPS
http://research.nhgri.nih.gov/ALPS/ |
Jennifer Puck, Stephen Straus, Michael Lenardo, Janet Dale, Joie Davis, Lilia Lei Bi, Jin Wang, NIAID & NHGRI, NIH, U.S.A. |
FAS
Fas (TNF receptor superfamily, member 6) 134637 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=FAS |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
FASLG
Fas ligand (TNF superfamily, member 6) 134638 |
FASLGbase: Mutation registry for Autoimmune lymphoproliferative syndrome, type 1B (ALPS1B) (previously known as TNFSF6base)
http://bioinf.uta.fi/FASLGbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
FASLG
Fas ligand (TNF superfamily, member 6) 134638 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=FASLG |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
FATE1
fetal and adult testis expressed 1 300450 |
FATE1 database at LOVD
http://www.LOVD.nl/FATE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FBN1
fibrillin 1 134797 |
The UMD FBN1 mutations database
http://www.umd.be/FBN1/ |
Gwenaelle Collod-Beroud, Laboratoire de g�n�tique Mol�culaire et Chromosomique, Montpellier, France |
FBN2
fibrillin 2 612570 |
The UMD FBN2 mutations database
http://194.167.35.168/FBN2/ |
G. Collod-B�roud |
FCGR1A
Fc fragment of IgG, high affinity Ia, receptor (CD64) 146760 |
FCGR1Abase: Mutation registry for CD64 deficiency
http://bioinf.uta.fi/FCGR1Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
FCGR3A
Fc fragment of IgG, low affinity IIIa, receptor (CD16a) 146740 |
FCGR3Abase: Mutation registry for Natural killer cell deficiency
http://bioinf.uta.fi/FCGR3Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
FGA
fibrinogen alpha chain 134820 |
A Database For Human Fibrinogen Variants
http://www.geht.org/databaseang/fibrinogen/ |
Michel Hanss, Laboratoire d�h�matologie, Hospices Civils de Lyon, France |
FGB
fibrinogen beta chain 134830 |
A Database For Human Fibrinogen Variants
http://www.geht.org/databaseang/fibrinogen/ |
Michel Hanss, Laboratoire d�h�matologie, Hospices Civils de Lyon, France |
FGD1
FYVE, RhoGEF and PH domain containing 1 300546 |
FGD1 database at LOVD
http://www.LOVD.nl/FGD1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FGG
fibrinogen gamma chain 134850 |
A Database For Human Fibrinogen Variants
http://www.geht.org/databaseang/fibrinogen/ |
Michel Hanss, Laboratoire d�h�matologie, Hospices Civils de Lyon, France |
FH
fumarate hydratase 136850 |
FH database at LOVD
http://www.LOVD.nl/FH |
Jean-Pierre Bayley, LUMC, Leiden |
FHL1
four and a half LIM domains 1 300163 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/FHL1 |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
FIGF
c-fos induced growth factor (vascular endothelial growth factor D) 300091 |
FIGF database at LOVD
http://www.LOVD.nl/FIGF |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FKBP10
FK506 binding protein 10, 65 kDa 607063 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, UK. |
FKRP
fukutin related protein 606596 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/FKRP |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands & Ros�rio dos Santos, Centro de Gen�tica M�dica J., Magalh�es, INSA, Portugal |
FKTN
fukutin 607440 |
FCMD - Fukuyama type congenital muscular dystrophy
http://www.LOVD.nl/FKTN |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands & Ros�rio dos Santos, Centro de Gen�tica M�dica J., Magalh�es, INSA, Portugal |
FLCN
folliculin 607273 |
Folliculin (FLCN) variation database
http://www.lovd.nl/FLCN |
Dr. Derek Lim, Prof. Eamonn Maher, European Birt-Hogg-Dube Consortium, University of Birmingham School of Medicine, UK |
FLCN
folliculin 607273 |
The Folliculin Mutation Database
http://skingenedatabase.com/ |
Database Administration |
FLNA
filamin A, alpha 300017 |
Filamin A, alpha (FLNA) Mental Retardation Database
http://www.LOVD.nl/FLNA |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands |
FLNC
filamin C, gamma 102565 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/FLNC |
Johan T den Dunnen Leiden Univ. Med Centre |
FLT1
fms-related tyrosine kinase 1 (vascular endothelial growth factor/vascular permeability factor receptor) 165070 |
Fms-related tyrosine kinase 1 (FLT1) database
http://lovd.bx.psu.edu/home.php?select_db=FLT1 |
Belinda Giardine and Joseph Borg |
FMO3
flavin containing monooxygenase 3 136132 |
The Homo sapients FMO3 Allelic Variant Database
http://human-fmo3.biochem.ucl.ac.uk/Human_FMO3/ |
Elizabeth A. Shephard, Sarah Addou Dept. Biochem. & Molecular Biol. Univ. College London. UK Ian R. Phillips Sch. Bio. Sc. Queen Mary, Univ. of London , UK |
FMR1
fragile X mental retardation 1 309550 |
FMR1 database at LOVD
http://www.LOVD.nl/FMR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FMR1NB
fragile X mental retardation 1 neighbor |
FMR1NB database at LOVD
http://www.LOVD.nl/FMR1NB |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FOXL2
forkhead box L2 605597 |
The Human FOXL2 Allelic Variant Database
http://medgen.ugent.be/LOVD2/home.php?select_db=FOXL2 |
Diane Beysen, Elfride de Baere Centre for Medical Genetics Gent, Belgium |
FOXN1
forkhead box N1 600838 |
FOXN1base: Mutation registry for T-cell immunodeficiency, congenital alopecia, and nail dystrophy (Previously known as WHNbase)
http://bioinf.uta.fi/FOXN1base/ |
Mauno Vihinen & Claudio Pignata, Univ. of Tampere, Tampere, Finland |
FOXO4
forkhead box O4 300033 |
FOXO4 database at LOVD
http://www.LOVD.nl/FOXO4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FOXP3
forkhead box P3 300292 |
FOXP3base: Mutation registry for Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked; IPEX
http://bioinf.uta.fi/FOXP3base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
FOXP3
forkhead box P3 300292 |
FOXP3 database at LOVD
http://www.LOVD.nl/FOXP3 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FOXP3
forkhead box P3 300292 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=FOXP3 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
FOXR2
forkhead box R2 |
FOXR2 database at LOVD
http://www.LOVD.nl/FOXR2 |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
FRMD7
FERM domain containing 7 300628 |
FRMD7 database at LOVD
http://www.LOVD.nl/FRMD7 |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
FRMPD3
FERM and PDZ domain containing 3 |
FRMPD3 database at LOVD
http://www.LOVD.nl/FRMPD3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FRMPD4
FERM and PDZ domain containing 4 |
FRMPD4 database at LOVD
http://www.LOVD.nl/FRMPD4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FSCN2
fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus) 607643 |
Mutations of the Fascin Gene
http://www.retina-international.org/sci-news/fscn2mut.htm |
Retina International |
FTHL17
ferritin, heavy polypeptide-like 17 300308 |
FTHL17 database at LOVD
http://www.LOVD.nl/FTHL17 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FTSJ1
FtsJ homolog 1 (E. coli) 300499 |
FTSJ1 database at LOVD
http://www.LOVD.nl/FTSJ1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FUNDC1
FUN14 domain containing 1 |
FUNDC1 database at LOVD
http://www.LOVD.nl/FUNDC1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
FUT1
fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group) 211100 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
FUT2
fucosyltransferase 2 (secretor status included) 182100 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry; Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
FUT3
fucosyltransferase 3 (galactoside 3(4)-L-fucosyltransferase, Lewis blood group) 111100 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology,Albert Einstein College of Medicine New York, NY. U.S.A |
FUT6
fucosyltransferase 6 (alpha (1,3) fucosyltransferase) 136836 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
FUT7
fucosyltransferase 7 (alpha (1,3) fucosyltransferase) 602030 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine New York, NY. U.S.A |
Go Back To Main Index! | ||
G6PD
glucose-6-phosphate dehydrogenase 305900 |
G6PD Mutations
http://www.bioinf.org.uk/g6pd/ |
Colin Kwok, Department of Biochemistry, Faculty of Medicine, The University of Hong Kong & Andrew C.R. Martin Department of Biochemistry and Molecular Biology, University College London |
G6PD
glucose-6-phosphate dehydrogenase 305900 |
G6PD database at LOVD
http://www.LOVD.nl/G6PD |
Mental Retardation database |
GAA
glucosidase, alpha; acid 606800 |
GAA - Pompe disease (glycogen storage disease type II)
http://www.LOVD.nl/GAA |
Johan T. den Dunnen, LUMC, The Netherlands, Arnold Reuser & Marian Kroos, EUR, Rotterdam, Nederland |
GAA
glucosidase, alpha; acid 606800 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GAA |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
GAB3
GRB2-associated binding protein 3 300482 |
GAB3 database at LOVD
http://www.LOVD.nl/GAB3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GABRE
gamma-aminobutyric acid (GABA) A receptor, epsilon 300093 |
GABRE database at LOVD
http://www.LOVD.nl/GABRE |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GABRQ
gamma-aminobutyric acid (GABA) receptor, theta 300349 |
GABRQ database at LOVD
http://www.LOVD.nl/GABRQ |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GALT
galactose-1-phosphate uridylyltransferase 606999 |
Galactosaemia
http://www.ich.bris.ac.uk/galtdb/ |
Linda Tyfield, David Carmichael, Inst. Child Health, Univ. Bristol, Bristol, UK |
GALT
galactose-1-phosphate uridylyltransferase 606999 |
Galactose-1-Phosphate Uridyl Transferase (GALT) Mutation Database
http://arup.utah.edu/database/galactosemia/GALT_welcome.php |
Rong Mao and Fernanda Calderon, Department of Pathology, University of Utah, USA. |
GAMT
guanidinoacetate N-methyltransferase 601240 |
Guanidinoacetate N-methyltransferase (GAMT) Variation Database
http://www.LOVD.nl/GAMT |
Gajja Salomons |
GAN
gigaxonin 605379 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
GARS
glycyl-tRNA synthetase 600287 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
GATM
glycine amidinotransferase (L-arginine:glycine amidinotransferase) 602360 |
Guanidinoacetate N-methyltransferase (GAMT) Variation Database
http://www.LOVD.nl/GATM |
Gajja Salomons |
GBA
glucosidase, beta, acid 606463 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GBA |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
GCH1
GTP cyclohydrolase 1 600225 |
GTP Cyclohydrolase I deficiency; BIOMED/BIODEF database
http://www.bh4.org/ |
N. Blau, Univ. Children's Hospital,Zurich, J.L. Dhont- Facult� libre de M�dicine,Lille |
GCK
glucokinase (hexokinase 4) 138079 |
Monogenic Diabetes
http://www.LOVD.nl/GCK |
Monique Losekoot and Vincent Janmaat |
GCNT2
glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) 600429 |
GCNT2 database at LOVD
http://www.LOVD.nl/GCNT2 |
Johan T den Dunnen Leiden Univ. Med Centre |
GDAP1
ganglioside-induced differentiation-associated protein 1 606598 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
GDPD2
glycerophosphodiester phosphodiesterase domain containing 2 |
GDPD2 database at LOVD
http://www.LOVD.nl/GDPD2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GEMIN8
gem (nuclear organelle) associated protein 8 |
GEMIN8 database at LOVD
http://www.LOVD.nl/GEMIN8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GFI1
growth factor independent 1 transcription repressor 600871 |
GFI1base: Mutation registry for SCN and NI-CINA
http://bioinf.uta.fi/GFI1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
GHR
growth hormone receptor 600946 |
LOVD growth
http://www.LOVD.nl/GHR |
LA Metherell and MO Savage |
GIGYF2
GRB10 interacting GYF protein 2 612003 |
PARK11 Parkinson's disease Mutation Database
http://www.LOVD.nl/PARK11 |
The Parkinson's Institute |
GJA1
gap junction protein, alpha 1, 43kDa 121014 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
GJA1
gap junction protein, alpha 1, 43kDa 121014 |
The Connexin-deafness homepage
http://davinci.crg.es/deafness/ |
Ester Ballana, Marina Ventayol, Paolo Gasparini, Xavier Estivill, (CRG) Barcelona Spain |
GJA3
gap junction protein, alpha 3, 46kDa 121015 |
GJA3 database at LOVD
http://www.LOVD.nl/GJA3 |
Johan T den Dunnen Leiden Univ. Med Centre |
GJA8
gap junction protein, alpha 8, 50kDa 600897 |
GJA8 database at LOVD
http://www.LOVD.nl/GJA8 |
Johan T den Dunnen Leiden Univ. Med Centre |
GJB1
gap junction protein, beta 1, 32kDa 304040 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
GJB1
gap junction protein, beta 1, 32kDa 304040 |
The Connexin-deafness homepage
http://davinci.crg.es/deafness/ |
Ester Ballana, Marina Ventayol, Paolo Gasparini, Xavier Estivill, (CRG) Barcelona Spain |
GJB2
gap junction protein, beta 2, 26kDa 121011 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
GJB2
gap junction protein, beta 2, 26kDa 121011 |
The Connexin-deafness homepage
http://davinci.crg.es/deafness/ |
Ester Ballana, Marina Ventayol, Paolo Gasparini, Xavier Estivill, (CRG) Barcelona Spain |
GJB2
gap junction protein, beta 2, 26kDa 121011 |
The UMD DFNB1-GJB2 mutations database
http://www.umd.be/DFNB1-GJB2/ |
A.-F. Roux and D. Baux |
GJB2
gap junction protein, beta 2, 26kDa 121011 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GJB2 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
GJB3
gap junction protein, beta 3, 31kDa 603324 |
The Connexin-deafness homepage
http://davinci.crg.es/deafness/ |
Ester Ballana, Marina Ventayol, Paolo Gasparini, Xavier Estivill, (CRG) Barcelona Spain |
GJB3
gap junction protein, beta 3, 31kDa 603324 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
GJB6
gap junction protein, beta 6, 30kDa 604418 |
The Connexin-deafness homepage
http://davinci.crg.es/deafness/ |
Ester Ballana, Marina Ventayol, R Rabionet, Paolo Gasparini, Xavier Estivill, (CRG) Barcelona Spain |
GJB6
gap junction protein, beta 6, 30kDa 604418 |
Hereditary Hearing Loss Homepage
http://hereditaryhearingloss.org/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
GJB6
gap junction protein, beta 6, 30kDa 604418 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GJB6 |
Ammar Husami and Theru A. Sivakumaran |
GK
glycerol kinase 300474 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/GK |
Johan T. den Dunnen Leiden Univ. Med Centre |
GLA
galactosidase, alpha 300644 |
GLA database at LOVD
http://www.LOVD.nl/GLA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GLA
galactosidase, alpha 300644 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GLA |
Ammar Husami and Theru A. Sivakumaran |
GLOD5
glyoxalase domain containing 5 |
GLOD5 database at LOVD
http://www.LOVD.nl/GLOD5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GLRA1
glycine receptor, alpha 1 138491 |
GLRA1 database at LOVD
http://www.LOVD.nl/GLRA1 |
Ieke Ginjaar & Vincent Janmaat, LUMC, Leiden, The Netherlands |
GLRA2
glycine receptor, alpha 2 305990 |
GLRA2 database at LOVD
http://www.LOVD.nl/GLRA2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GLRA4
glycine receptor, alpha 4 |
GLRA4 database at LOVD
http://www.LOVD.nl/GLRA4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GLUD2
glutamate dehydrogenase 2 300144 |
GLUD2 database at LOVD
http://www.LOVD.nl/GLUD2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GM2A
GM2 ganglioside activator 272750 |
GM2A Locus Database
http://www.hexdb.mcgill.ca |
F. Kaplan, Paulo Cordeiro, McGill University, Montreal, Canada |
GNAS
GNAS complex locus 139320 |
LOVD - Leiden Open Variation Database
http://www.LOVD.nl/GNAS |
Johan T. den Dunnen |
GNAT2
guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2 139340 |
Mutations of the Transducin Subunits
http://www.retina-international.org/sci-news/gntmut.htm |
Retina International |
GNE
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase 603824 |
GNE database at LOVD
http://www.LOVD.nl/GNE |
Johan T den Dunnen Leiden Univ. Med Centre |
GNL3L
guanine nucleotide binding protein-like 3 (nucleolar)-like |
GNL3L database at LOVD
http://www.LOVD.nl/GNL3L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GP1BB
glycoprotein Ib (platelet), beta polypeptide 138720 |
Bernard-Soulier Syndrome database
http://www.bernardsoulier.org/index.html |
Dermot Kenny, Royal College of Surgeons in Ireland |
GP9
glycoprotein IX (platelet) 173515 |
Bernard-Soulier Syndrome database
http://www.bernardsoulier.org/index.html |
Dermot Kenny, Royal College of Surgeons in Ireland |
GPC4
glypican 4 300168 |
GPC4 database at LOVD
http://www.LOVD.nl/GPC4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPKOW
G patch domain and KOW motifs |
GPKOW database at LOVD
http://www.LOVD.nl/GPKOW |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
GPM6B
glycoprotein M6B 300051 |
GPM6B database at LOVD
http://www.LOVD.nl/GPM6B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPM6B
glycoprotein M6B 300051 |
Glycoprotein M6B (GPM6B) database
http://lovd.bx.psu.edu/home.php?select_db=GPM6B |
Belinda Giardine and Joseph Borg |
GPR101
G protein-coupled receptor 101 300393 |
GPR101 database at LOVD
http://www.LOVD.nl/GPR101 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR112
G protein-coupled receptor 112 |
GPR112 database at LOVD
http://www.LOVD.nl/GPR112 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR119
G protein-coupled receptor 119 300513 |
GPR119 database at LOVD
http://www.LOVD.nl/GPR119 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR143
G protein-coupled receptor 143 300500 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota |
GPR143
G protein-coupled receptor 143 300500 |
Mutations of the OA1 Gene
http://www.retina-international.org/sci-news/oa1mut.htm |
Retina International |
GPR173
G protein-coupled receptor 173 300253 |
GPR173 database at LOVD
http://www.LOVD.nl/GPR173 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR174
G protein-coupled receptor 174 |
GPR174 database at LOVD
http://www.LOVD.nl/GPR174 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR50
G protein-coupled receptor 50 300207 |
GPR50 database at LOVD
http://www.LOVD.nl/GPR50 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR64
G protein-coupled receptor 64 300572 |
GPR64 database at LOVD
http://www.LOVD.nl/GPR64 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR82
G protein-coupled receptor 82 300748 |
GPR82 database at LOVD
http://www.LOVD.nl/GPR82 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPR98
G protein-coupled receptor 98 602851 |
Retinal and hearing impairment genetic mutation database
http://www.LOVD.nl/GPR98 |
David Baux, Inserm |
GPR98
G protein-coupled receptor 98 602851 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=GPR98 |
Ammar Husami and Theru A. Sivakumaran |
GPRASP1
G protein-coupled receptor associated sorting protein 1 300417 |
GPRASP1 database at LOVD
http://www.LOVD.nl/GPRASP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GPRASP2
G protein-coupled receptor associated sorting protein 2 |
GPRASP2 database at LOVD
http://www.LOVD.nl/GPRASP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GRIA3
glutamate receptor, ionotrophic, AMPA 3 305915 |
GRIA3 database at LOVD
http://www.LOVD.nl/GRIA3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GRIPAP1
GRIP1 associated protein 1 300408 |
GRIPAP1 database at LOVD
http://www.LOVD.nl/GRIPAP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GRK1
G protein-coupled receptor kinase 1 180381 |
Mutations of the Rhodopsin Kinase Gene
http://www.retina-international.org/sci-news/rhokmut.htm |
Retina International |
GRPR
gastrin-releasing peptide receptor 305670 |
GRPR database at LOVD
http://www.LOVD.nl/GRPR |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GSPT2
G1 to S phase transition 2 300418 |
GSPT2 database at LOVD
http://www.LOVD.nl/GSPT2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GTPBP6
GTP binding protein 6 (putative) 300124 |
GTPBP6 database at LOVD
http://www.LOVD.nl/GTPBP6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GUCY2D
guanylate cyclase 2D, membrane (retina-specific) 600179 |
Mutations of the Retinal Guanylate Cyclase Gene and the Retinal Guanylate Cyclase-activating Protein Gene
http://www.retina-international.org/sci-news/gcmut.htm |
Retina International |
GUCY2F
guanylate cyclase 2F, retinal 300041 |
GUCY2F database at LOVD
http://www.LOVD.nl/GUCY2F |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GYG2
glycogenin 2 300198 |
GYG2 database at LOVD
http://www.LOVD.nl/GYG2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
GYPA
glycophorin A (MNS blood group) 111300 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
GYPB
glycophorin B (MNS blood group) 111740 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
GYPC
glycophorin C (Gerbich blood group) 110750 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
GYPE
glycophorin E (MNS blood group) 138590 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
Go Back To Main Index! | ||
H2BFWT
H2B histone family, member W, testis-specific 300507 |
H2BFWT database at LOVD
http://www.LOVD.nl/H2BFWT |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HAO2
hydroxyacid oxidase 2 (long chain) 605176 |
Hydroxyacid oxidase 2 (long chain) (HAO2) database
http://lovd.bx.psu.edu/home.php?select_db=HAO2 |
Belinda Giardine and Joseph Borg |
HAUS7
HAUS augmin-like complex, subunit 7 300540 |
HAUS7 database at LOVD
http://www.LOVD.nl/HAUS7 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HAX1
HCLS1 associated protein X-1 605998 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=HAX1 |
Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran |
HBA1
hemoglobin, alpha 1 141800 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBA1
hemoglobin, alpha 1 141800 |
Alpha-1 globin (HBA1) database
http://lovd.bx.psu.edu/home.php?select_db=HBA1 |
Belinda Giardine and Joseph Borg |
HBA2
hemoglobin, alpha 2 141850 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBA2
hemoglobin, alpha 2 141850 |
Alpha-2 globin (HBA2) database
http://lovd.bx.psu.edu/home.php?select_db=HBA2 |
Belinda Giardine and Joseph Borg |
HBB
hemoglobin, beta 141900 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBB
hemoglobin, beta 141900 |
Beta globin (HBB) database
http://lovd.bx.psu.edu/home.php?select_db=HBB |
Belinda Giardine and Joseph Borg |
HBD
hemoglobin, delta 142000 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBD
hemoglobin, delta 142000 |
Delta globin (HBD) database
http://lovd.bx.psu.edu/home.php?select_db=HBD |
Belinda Giardine and Joseph Borg |
HBG1
hemoglobin, gamma A 142200 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBG1
hemoglobin, gamma A 142200 |
A-gamma globin (HBG1) database
http://lovd.bx.psu.edu/home.php?select_db=HBG1 |
Belinda Giardine and Joseph Borg |
HBG2
hemoglobin, gamma G 142250 |
HbVar: A Database of Human Hemoglobin Variants and Thalassemias
http://globin.cse.psu.edu/globin/hbvar/menu.html |
Nick Anagnou IMBB, FORTH, Crete, Greece, David Chui, Boston Univ Med Cnt, USA, Ross Hardison, Dept. Biochem & Mol Biol, Penn State Univ USA, George Patrinos, Erasmus MC, the Netherlands, Henri Wajcman INSERM, H�pital Henri Mondor, France |
HBG2
hemoglobin, gamma G 142250 |
G-gamma globin (HBG2) databse
http://lovd.bx.psu.edu/home.php?select_db=HBG2 |
Belinda Giardine and Joseph Borg |
HBS1L
HBS1-like (S. cerevisiae) 612450 |
HBS1-like (HBS1L) database
http://lovd.bx.psu.edu/home.php?select_db=HBS1L |
Belinda Giardine and Joseph Borg |
HCCS
holocytochrome c synthase (cytochrome c heme-lyase) 300056 |
HCCS database at LOVD
http://www.LOVD.nl/HCCS |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HCFC1
host cell factor C1 (VP16-accessory protein) 300019 |
HCFC1 database at LOVD
http://www.LOVD.nl/HCFC1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HDAC6
histone deacetylase 6 300272 |
HDAC6 database at LOVD
http://www.LOVD.nl/HDAC6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HDAC8
histone deacetylase 8 300269 |
HDAC8 database at LOVD
http://www.LOVD.nl/HDAC8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HDHD1A
haloacid dehalogenase-like hydrolase domain containing 1A 306480 |
HDHD1A database at LOVD
http://www.LOVD.nl/HDHD1A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HDX
highly divergent homeobox |
http://www.LOVD.nl/HDX
http://www.LOVD.nl/HAUS7 |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
HEPH
hephaestin 300167 |
HEPH database at LOVD
http://www.LOVD.nl/HEPH |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HEXA
hexosaminidase A (alpha polypeptide) 606869 |
Hexosaminidase A; Tay-Sachs Disease
http://www.hexdb.mcgill.ca |
Feige Kaplan, Manyphong Phommarinh, McGill Univ. Montreal, Canada |
HEXB
hexosaminidase B (beta polypeptide) 606873 |
HEXB Locus Database
http://www.hexdb.mcgill.ca |
F. Kaplan, Paulo Cordeiro, Manyphong Phommarinh, McGill University, Montreal, Canada |
HGD
homogentisate 1,2-dioxygenase 607474 |
AKUdatabaseHomogentisate 1,2 Dioxygenase Locus (HGO) Mutation and Polymorphism Database Home Page
http://www.alkaptonuria.cib.csic.es/index.htm |
Santiago Rodr�guez de C�rdoba & Daniel Beltr�n-Valero de Bernab�Centro de Investigaciones Biol�gicas (CSIC) Vel�zquez, Madrid, Spain (Inactive) |
HGSNAT
heparan-alpha-glucosaminide N-acetyltransferase 610453 |
LOVD - Leiden Open Variation Database
http://www.LOVD.nl/HGSNAT |
St�phanie Durand |
HLA-A
major histocompatibility complex, class I, A 142800 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-B
major histocompatibility complex, class I, B 142830 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-C
major histocompatibility complex, class I, C 142840 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DMA
major histocompatibility complex, class II, DM alpha 142855 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DMB
major histocompatibility complex, class II, DM beta 142856 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DOA
major histocompatibility complex, class II, DO alpha 142930 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DOB
major histocompatibility complex, class II, DO beta 600629 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DPA1
major histocompatibility complex, class II, DP alpha 1 142880 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DPA2
major histocompatibility complex, class II, DP alpha 2 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DPA3
major histocompatibility complex, class II, DP alpha 3 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DPB1
major histocompatibility complex, class II, DP beta 1 142858 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DPB2
major histocompatibility complex, class II, DP beta 2 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DQA1
major histocompatibility complex, class II, DQ alpha 1 146880 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DQA2
major histocompatibility complex, class II, DQ alpha 2 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DQB1
major histocompatibility complex, class II, DQ beta 1 604305 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DQB2
major histocompatibility complex, class II, DQ beta 2 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DQB3
major histocompatibility complex, class II, DQ beta 3 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRA
major histocompatibility complex, class II, DR alpha 142860 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB1
major histocompatibility complex, class II, DR beta 1 142857 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB2
major histocompatibility complex, class II, DR beta 2 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB3
major histocompatibility complex, class II, DR beta 3 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB4
major histocompatibility complex, class II, DR beta 4 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB5
major histocompatibility complex, class II, DR beta 5 604776 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB6
major histocompatibility complex, class II, DR beta 6 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB7
major histocompatibility complex, class II, DR beta 7 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB8
major histocompatibility complex, class II, DR beta 8 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-DRB9
major histocompatibility complex, class II, DR beta 9 (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-E
major histocompatibility complex, class I, E 143010 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-F
major histocompatibility complex, class I, F 143110 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-G
major histocompatibility complex, class I, G 142871 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-H
major histocompatibility complex, class I, H (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-J
major histocompatibility complex, class I, J (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-K
major histocompatibility complex, class I, K (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-L
major histocompatibility complex, class I, L, pseudogene |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-N
major histocompatibility complex, class I, N (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-P
major histocompatibility complex, class I, P (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-S
major histocompatibility complex, class I, S (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-T
major histocompatibility complex, class I, T (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-U
major histocompatibility complex, class I, U (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-V
major histocompatibility complex, class I, V (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-W
major histocompatibility complex, class I, W (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-X
major histocompatibility complex, class I, X (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-Y
major histocompatibility complex, class I, Y (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HLA-Z
major histocompatibility complex, class I, Z (pseudogene) |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
HMGCS2
3-hydroxy-3-methylglutaryl-CoA synthase 2 (mitochondrial) 600234 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=HMGCS2 |
Stefanie Kalb |
HMGN5
high-mobility group nucleosome binding domain 5 300385 |
HMGN5 database at LOVD
http://www.LOVD.nl/HMGN5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HNF1A
HNF1 homeobox A 142410 |
HNF1A at LOVD
http://www.LOVD.nl/HNF1A |
Monique Losekoot, LUMC, Leiden, Netherlands |
HNF4A
hepatocyte nuclear factor 4, alpha 600281 |
HNF4A at LOVD
http://www.LOVD.nl/HNF4A |
Monique Losekoot, LUMC, Leiden, Netherlands |
HNRNPH2
heterogeneous nuclear ribonucleoprotein H2 (H') 300610 |
HNRNPH2 database at LOVD
http://www.LOVD.nl/HNRNPH2 |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
HPRT1
hypoxanthine phosphoribosyltransferase 1 308000 |
Hypoxanthine Guanine Phosphoribosyltransferase 1; Lech-Nyhan Syndrome
http://www.ibiblio.org/dnam/mainpage.html |
Neil Cariello, Univ. Nth Carolina, USA |
HPS1
Hermansky-Pudlak syndrome 1 604982 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota, USA |
HPS1
Hermansky-Pudlak syndrome 1 604982 |
Mutations of the ep-Gene
http://www.retina-international.org/sci-news/epmut.htm |
Retina International |
HPS1
Hermansky-Pudlak syndrome 1 604982 |
Mutations of the HPS Gene
http://www.retina-international.org/sci-news/hpsmut.htm |
Retina International |
HPS3
Hermansky-Pudlak syndrome 3 606118 |
Mutations of the HPS3 Gene
http://www.retina-international.org/sci-news/hps3mut.htm |
Retina International |
HPS3
Hermansky-Pudlak syndrome 3 606118 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota, USA |
HPS4
Hermansky-Pudlak syndrome 4 606682 |
Mutations of the Human light ear Gene (le, HPS4)
http://www.retina-international.org/sci-news/lemut.htm |
Retina International |
HS6ST2
heparan sulfate 6-O-sulfotransferase 2 300545 |
HS6ST2 database at LOVD
http://www.LOVD.nl/HS6ST2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HSD17B10
hydroxysteroid (17-beta) dehydrogenase 10 300256 |
HSD17B10 database at LOVD
http://www.LOVD.nl/HSD17B10 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HSD17B10
hydroxysteroid (17-beta) dehydrogenase 10 300256 |
Innsbruck Metabolic Diseases Pages
http://lovd.i-med.ac.at/home.php?select_db=HSD17B10 |
Johannes Zschocke |
HSF4
heat shock transcription factor 4 602438 |
HSF4 database at LOVD
http://www.LOVD.nl/HSF4 |
Johan T den Dunnen Leiden Univ. Med Centre |
HSN2
hereditary sensory neuropathy, type II 608620 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
HSPB1
heat shock 27kDa protein 1 602195 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
HSPB8
heat shock 22kDa protein 8 608014 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
HTATSF1
HIV-1 Tat specific factor 1 300346 |
HTATSF1 database at LOVD
http://www.LOVD.nl/HTATSF1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HTR2C
5-hydroxytryptamine (serotonin) receptor 2C 312861 |
HTR2C database at LOVD
http://www.LOVD.nl/HTR2C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
HTR3A
5-hydroxytryptamine (serotonin) receptor 3A 182139 |
HTR3A database at Heidelberg University
http://hyg-serv-01.hyg.uni-heidelberg.de/lovd/index.php?select_db=HTR3A |
Steffi Wilke and Dr. Beate Niesler, Heidelberg University |
HUWE1
HECT, UBA and WWE domain containing 1 300697 |
HUWE1 database at LOVD
http://www.LOVD.nl/HUWE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
ICAM4
intercellular adhesion molecule 4 (Landsteiner-Wiener blood group) 111250 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
ICOS
inducible T-cell co-stimulator 604558 |
ICOSbase: Mutation registry for ICOS deficiency
http://bioinf.uta.fi/ICOSbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IDS
iduronate 2-sulfatase 309900 |
IDS database at LOVD
http://www.LOVD.nl/IDS |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IFNGR1
interferon gamma receptor 1 107470 |
IFNGR1base: Mutation registry for IFNγ1-receptor deficiency
http://bioinf.uta.fi/IFNGR1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IFNGR2
interferon gamma receptor 2 (interferon gamma transducer 1) 147569 |
IFNGR2base: Mutation registry for IFNγ2-receptor deficiency
http://bioinf.uta.fi/IFNGR2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IGBP1
immunoglobulin (CD79A) binding protein 1 300139 |
IGBP1 database at LOVD
http://www.LOVD.nl/IGBP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IGF1
insulin-like growth factor 1 (somatomedin C) 147440 |
LOVD growth
http://www.LOVD.nl/IGF1 |
Jan Maarten Wit and Marie-Jose Walenkamp |
IGF1R
insulin-like growth factor 1 receptor 147370 |
LOVD growth
http://www.LOVD.nl/IGF1R |
Roland Pfaeffle and Wieland Kiess |
IGF2
insulin-like growth factor 2 (somatomedin A) 147470 |
LOVD growth
http://www.LOVD.nl/IGF2 |
Irene Netchine and Yves le Bouc |
IGFALS
insulin-like growth factor binding protein, acid labile subunit 601489 |
IGFALS database at LOVD
http://www.LOVD.nl/IGFALS |
H Jasper and HM Domen� |
IGHC
Immunoglobulin heavy constant group |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr/ |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGHD
immunoglobulin heavy constant delta 147170 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGHG2
immunoglobulin heavy constant gamma 2 (G2m marker) 147110 |
IGHG2base: Mutation registry for IgG2 deficiency
http://bioinf.uta.fi/IGHG2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IGHJ2
immunoglobulin heavy joining 2 147010 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGHM
immunoglobulin heavy constant mu 147020 |
IGHMbase: Mutation registry for � heavy-chain deficiency
http://bioinf.uta.fi/IGHMbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IGHMBP2
immunoglobulin mu binding protein 2 600502 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
IGHV@
immunoglobulin heavy variable group 147070 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGKC
immunoglobulin kappa constant 147200 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGKJ@
immunoglobulin kappa joining group 146970 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGKV@
immunoglobulin kappa variable group 146980 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGLC1
immunoglobulin lambda constant 1 (Mcg marker) 147220 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGLJ@
immunoglobulin lambda joining group 147230 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGLL1
immunoglobulin lambda-like polypeptide 1 146770 |
IGLL1base: Mutation registry for λ 5 surrogate light-chain deficiency
http://bioinf.uta.fi/IGLL1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IGLV@
immunoglobulin lambda variable group 147240 |
IMGT; the international ImMunoGeneTics information system �
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
IGSF1
immunoglobulin superfamily, member 1 300137 |
IGSF1 database at LOVD
http://www.LOVD.nl/IGSF1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IKBKAP
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein 603722 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
IKBKG
inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 300248 |
IKBKGbase: Mutation registry for Nemo deficiency
http://bioinf.uta.fi/IKBKGbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IL12B
interleukin 12B (natural killer cell stimulatory factor 2, cytotoxic lymphocyte maturation factor 2, p40) 161561 |
IL12Bbase: Mutation registry for Interleukin-12 (IL-12) p40 deficiency
http://bioinf.uta.fi/IL12Bbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IL12RB1
interleukin 12 receptor, beta 1 601604 |
IL12RB1base: Mutation registry for Interleukin-12 receptor �1 deficiency
http://bioinf.uta.fi/IL12RB1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IL13RA1
interleukin 13 receptor, alpha 1 300119 |
IL13RA1 database at LOVD
http://www.LOVD.nl/IL13RA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IL13RA2
interleukin 13 receptor, alpha 2 300130 |
IL13RA2 database at LOVD
http://www.LOVD.nl/IL13RA2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IL1RAPL1
interleukin 1 receptor accessory protein-like 1 300206 |
IL1RAPL1 database at LOVD
http://www.LOVD.nl/IL1RAPL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IL1RAPL2
interleukin 1 receptor accessory protein-like 2 300277 |
IL1RAPL2 database at LOVD
http://www.LOVD.nl/IL1RAPL2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IL2RA
interleukin 2 receptor, alpha 147730 |
IL2RAbase: Mutation registry for Interleuken 2 receptor α deficiency
http://bioinf.uta.fi/IL2RAbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IL2RG
interleukin 2 receptor, gamma 308380 |
X-Linked Severe Combined Immuno deficiency SCID
http://research.nhgri.nih.gov/apps/scid/IL2RGbase.shtml |
Jeniffer Puck, Joie Davies, Roxanne Fisher, Amy Pepper, NHGRI/NIH, Bethesda |
IL2RG
interleukin 2 receptor, gamma 308380 |
CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=IL2RG |
Ammar Husami and Theru A. Sivakumaran |
IL2RG
interleukin 2 receptor, gamma 308380 |
IL2RG database at LOVD
http://www.LOVD.nl/IL2RG |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IL7R
interleukin 7 receptor 146661 |
IL7Rbase: Mutation registry for Interleukin-7 receptor α deficiency
http://bioinf.uta.fi/IL7Rbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IL9R
interleukin 9 receptor 300007 |
IL9R database at LOVD
http://www.LOVD.nl/IL9R |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IMPDH1
IMP (inosine monophosphate) dehydrogenase 1 146690 |
Mutations of the Inosine Monophosphate DehydrogenaseType 1 Gene
http://www.retina-international.org/sci-news/impdhmut.htm |
Retina International |
INE1
inactivation escape 1 (non-protein coding) 300164 |
INE1 database at LOVD
http://www.LOVD.nl/INE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IQSEC2
IQ motif and Sec7 domain 2 300522 |
IQSEC2 database at LOVD
http://www.LOVD.nl/IQSEC2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IRAK1
interleukin-1 receptor-associated kinase 1 300283 |
IRAK1 database at LOVD
http://www.LOVD.nl/IRAK1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
IRAK4
interleukin-1 receptor-associated kinase 4 606883 |
IRAK4base: Mutation registry for IRAK4 deficiency
http://bioinf.uta.fi/IRAK4base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
IRS4
insulin receptor substrate 4 603510 |
IRS4 database at LOVD
http://www.LOVD.nl/IRS4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ISCU
iron-sulfur cluster scaffold homolog (E. coli) 611911 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/ISCU |
Johan T den Dunnen Leiden Univ. Med Centre |
ITGA2B
integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41) 607759 |
Glanzmann Thrombasthenia Database (GPIIb)
http://sinaicentral.mssm.edu/intranet/research/glanzmann/menu |
Dr. David Wilcox, Mount Sinai School of Medicine, U.S.A. |
ITGA7
integrin, alpha 7 600536 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/ITGA7 |
Johan T den Dunnen Leiden Univ. Med Centre |
ITGB2
integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) 600065 |
ITGB2base: Mutation registry for Leukocyte adhesion deficiency I (LAD-I)
http://bioinf.uta.fi/ITGB2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
ITGB3
integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) 173470 |
Glanzmann Thrombasthenia Database (GPIIIa)
http://sinaicentral.mssm.edu/intranet/research/glanzmann/menu |
Dr. David Wilcox, Mount Sinai School of Medicine, U.S.A. |
ITIH5L
inter-alpha (globulin) inhibitor H5-like |
ITIH5L database at LOVD
http://www.LOVD.nl/ITIH5L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ITM2A
integral membrane protein 2A 300222 |
ITM2A database at LOVD
http://www.LOVD.nl/ITM2A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
JAG1
jagged 1 601920 |
CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=JAG1 |
Ammar Husami and Theru A. Sivakumaran |
JAG1
jagged 1 601920 |
Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)
http://genomed.org/LOVD/ALGS/home.php?select_db=JAG1 |
Ming Qi, PhD, FACMG, Peikuan Cong and Min Pan |
JAK3
Janus kinase 3 600173 |
JAK3base: Mutation registry for autosomal recessive severe combined JAK3 deficiency
http://bioinf.uta.fi/JAK3base/ |
Luigi D. Notarangelo, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
JUP
junction plakoglobin 173325 |
Gene Connection for the Heart; Naxos disease database
http://www.fsm.it/cardmoc/ |
S.G. N. Protonotarios, Naxos, Greece & C. Napolitano, Pavia, Italy |
JUP
junction plakoglobin 173325 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
Go Back To Main Index! | ||
KAL1
Kallmann syndrome 1 sequence 308700 |
KAL1 database at LOVD
http://www.LOVD.nl/KAL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KCND1
potassium voltage-gated channel, Shal-related subfamily, member 1 300281 |
KCND1 database at LOVD
http://www.LOVD.nl/KCND1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KCNE1
potassium voltage-gated channel, Isk-related family, member 1 176261 |
Long QT Syndrome Database
http://www.ssi.dk/graphics/html/lqtsdb/lqtsdb.htm |
Michael Christiansen, Lars A. Larsen, Paal Skytt Andersen, Molecular Cardiology grp, Statens Serum Institut, Copenhagen, Denmark |
KCNE1
potassium voltage-gated channel, Isk-related family, member 1 176261 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
KCNE1
potassium voltage-gated channel, Isk-related family, member 1 176261 |
Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)
http://genomed.org/LOVD/LQTs/home.php?select_db=KCNE1 |
Ming Qi, PhD, FACMG, Peikuan Cong and Tao Zhang |
KCNE1
potassium voltage-gated channel, Isk-related family, member 1 176261 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=KCNE1 |
Ammar Husami and Theru A. Sivakumaran |
KCNE1L
KCNE1-like 300328 |
KCNE1L database at LOVD
http://www.LOVD.nl/KCNE1L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KCNE2
potassium voltage-gated channel, Isk-related family, member 2 603796 |
Long QT Syndrome Database
http://www.ssi.dk/graphics/html/lqtsdb/lqtsdb.htm |
Michael Christiansen, Lars A. Larsen, Paal Skytt Andersen, Molecular Cardiology grp, Statens Serum Institut, Copenhagen, Denmark |
KCNE2
potassium voltage-gated channel, Isk-related family, member 2 603796 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
KCNE2
potassium voltage-gated channel, Isk-related family, member 2 603796 |
Zhejiang University-Adinovo Center KCNE2 Database
http://www.china-hvp.org/LOVD/?select_db=KCNE2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
KCNH2
potassium voltage-gated channel, subfamily H (eag-related), member 2 152427 |
Long QT Syndrome Database
http://www.ssi.dk/graphics/html/lqtsdb/lqtsdb.htm |
Michael Christiansen, Lars A. Larsen, Paal Skytt Andersen, Molecular Cardiology grp, Statens Serum Institut, Copenhagen, Denmark |
KCNH2
potassium voltage-gated channel, subfamily H (eag-related), member 2 152427 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
KCNH2
potassium voltage-gated channel, subfamily H (eag-related), member 2 152427 |
Zhejiang University-Adinovo Center KCNH2 Database
http://www.china-hvp.org/LOVD/?select_db=KCNH2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
KCNJ2
potassium inwardly-rectifying channel, subfamily J, member 2 600681 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
KCNJ2
potassium inwardly-rectifying channel, subfamily J, member 2 600681 |
Zhejiang University-Adinovo Center KCNJ2 Database
http://www.china-hvp.org/LOVD/?select_db=KCNJ2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
KCNQ1
potassium voltage-gated channel, KQT-like subfamily, member 1 607542 |
Long QT Syndrome Database
http://www.ssi.dk/graphics/html/lqtsdb/lqtsdb.htm |
Michael Christiansen, Lars A. Larsen, Paal Skytt Andersen, Molecular Cardiology grp, Statens Serum Institut, Copenhagen, Denmark |
KCNQ1
potassium voltage-gated channel, KQT-like subfamily, member 1 607542 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
S.G. Priori, P.J. Schwartz, Pavia, Italy |
KCNQ1
potassium voltage-gated channel, KQT-like subfamily, member 1 607542 |
Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)
http://genomed.org/LOVD/LQTs/home.php?select_db=KCNQ1 |
Ming Qi, PhD, FACMG, Peikuan Cong and Tao Zhang |
KCNQ1
potassium voltage-gated channel, KQT-like subfamily, member 1 607542 |
CCHMC - Human Genetics Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=KCNQ1 |
Ammar Husami and Theru A. Sivakumaran |
KDM5C
lysine (K)-specific demethylase 5C 314690 |
KDM5C database at LOVD
http://www.LOVD.nl/KDM5C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KDM6A
lysine (K)-specific demethylase 6A 300128 |
KDM6A database at LOVD
http://www.LOVD.nl/KDM6A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KDR
kinase insert domain receptor (a type III receptor tyrosine kinase) 191306 |
Kinase insert domain receptor (KDR) database
http://lovd.bx.psu.edu/home.php?select_db=KDR |
Belinda Giardine and Joseph Borg |
KEL
Kell blood group, metallo-endopeptidase 110900 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
KIAA2022
KIAA2022 300524 |
KIAA2022 database at LOVD
http://www.LOVD.nl/KIAA2022 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KIF1B
kinesin family member 1B 605995 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
KIF4A
kinesin family member 4A 300521 |
KIF4A database at LOVD
http://www.LOVD.nl/KIF4A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KIR2DL1
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1 604936 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DL2
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2 604937 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DL3
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3 604938 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DL4
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4 604945 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DL5A
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A 605305 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DL5B
killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B 605305 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DP1
killer cell immunoglobulin-like receptor, two domains, pseudogene 1 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DS1
killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 1 604952 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DS2
killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2 604953 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DS3
killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 3 604954 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DS4
killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 4 604955 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR2DS5
killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 5 604956 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR3DL1
killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1 604946 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR3DL2
killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2 604947 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR3DL3
killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3 610095 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR3DP1
killer cell immunoglobulin-like receptor, three domains, pseudogene 1 610604 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KIR3DS1
killer cell immunoglobulin-like receptor, three domains, short cytoplasmic tail, 1 604946 |
IPD-KIR Database
http://www.ebi.ac.uk/ipd/kir/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
KL
klotho 604824 |
Klotho (KL) database
http://lovd.bx.psu.edu/home.php?select_db=KL |
Belinda Giardine and Joseph Borg |
KLF1
Kruppel-like factor 1 (erythroid) 600599 |
The Globin Gene Server
http://www.LOVD.nl/KLF1 |
Belinda Giardine and Joseph Borg |
KLHL13
kelch-like 13 (Drosophila) 300655 |
KLHL13 database at LOVD
http://www.LOVD.nl/KLHL13 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KLHL15
kelch-like 15 (Drosophila) |
KLHL15 database at LOVD
http://www.LOVD.nl/KLHL15 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
KLHL4
kelch-like 4 (Drosophila) 300348 |
KLHL4 database at LOVD
http://www.LOVD.nl/KLHL4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
L1CAM
L1 cell adhesion molecule 308840 |
L1CAM Mutation Web Page
http://www.l1cammutationdatabase.info |
Yvonne Vos Department of clinical genetics, University Medical Center Groningen, Groningen , The Netherlands |
L1CAM
L1 cell adhesion molecule 308840 |
NGRL, Manchester L1CAM database
http://ngrl.man.ac.uk/lovd2/home.php?select_db=L1CAM |
Bharathi Kattamuri and Simon Ramsden |
L1CAM
L1 cell adhesion molecule 308840 |
L1 cell adhesion molecule (L1CAM) database at LOVD
http://www.LOVD.nl/L1CAM |
Yvonne Vos, Department of Genetics University Medical Center Groningen,The Netherlands |
L2HGDH
L-2-hydroxyglutarate dehydrogenase 609584 |
L-2-hydroxyglutarate dehydrogenase (L2HGDH) at LOVD
http://www.LOVD.nl/L2HGDH |
Gajja Salomons |
LAMA2
laminin, alpha 2 156225 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/LAMA2 |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands |
LAMP2
lysosomal-associated membrane protein 2 309060 |
LAMP2 database at LOVD
http://www.LOVD.nl/LAMP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LANCL3
LanC lantibiotic synthetase component C-like 3 (bacterial) |
LANCL3 database at LOVD
http://www.LOVD.nl/LANCL3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LARGE
like-glycosyltransferase 603590 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/LARGE |
Johan den Dunnen, LUMC, Leiden, Nederland |
LAS1L
LAS1-like (S. cerevisiae) |
LAS1L database at LOVD
http://www.LOVD.nl/LAS1L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LDB3
LIM domain binding 3 605906 |
LDB3 - Leiden Muscular Dystrophy pages
http://www.LOVD.nl/LDB3 |
Johan den Dunnen and Montse Oliv� |
LDLR
low density lipoprotein receptor 606945 |
Hypercholesterolemia, Familial
http://www.ucl.ac.uk/ldlr/LOVDv.1.1.0/ |
Sarah Leigh, Dept. of Medicine, UCL |
LDLR
low density lipoprotein receptor 606945 |
UMD Locus Specific Databases
http://www.umd.be/LDLR/ |
M. Varret, C. Boileau, INSERM,Hopital Necker, Enfants Malades,Paris |
LDLRAP1
low density lipoprotein receptor adaptor protein 1 605747 |
Leiden Muscular Dystrophy pages
http://www.ucl.ac.uk/ldlr/Current/index.php?select_db=LDLRAP1 |
Sarah Leigh |
LEPRE1
leucine proline-enriched proteoglycan (leprecan) 1 610339 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
LHFPL1
lipoma HMGIC fusion partner-like 1 300566 |
LHFPL1 database at LOVD
http://www.LOVD.nl/LHFPL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LIG1
ligase I, DNA, ATP-dependent 126391 |
LIG1base: Mutation registry for DNA ligase I deficiency
http://bioinf.uta.fi/LIG1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
LIG4
ligase IV, DNA, ATP-dependent 601837 |
LIG4base: Mutation registry for LIG4 syndrome
http://bioinf.uta.fi/LIG4base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
LIM2
lens intrinsic membrane protein 2, 19kDa 154045 |
LIM2 database at LOVD
http://www.LOVD.nl/LIM2 |
Johan T den Dunnen Leiden Univ. Med Centre |
LITAF
lipopolysaccharide-induced TNF factor 603795 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB, University of Antwerp (UA), Belgium |
LMBRD1
LMBR1 domain containing 1 612625 |
Zhejiang University Center for Genetic and Genomic Medicine - LMBRD1
http://www.genomed.org/LOVD/mma/home.php?select_db=LMBRD1 |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
LMNA
lamin A/C 150330 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB, University of Antwerp (UA), Belgium |
LMNA
lamin A/C 150330 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/LMNA |
Johan T. den Dunnen Leiden Univ. Medical Centre Leiden, Netherlands |
LMNA
lamin A/C 150330 |
The LMNA mutations database
http://www.umd.be/LMNA/ |
G. Bonne, France |
LONRF3
LON peptidase N-terminal domain and ring finger 3 |
LONRF3 database at LOVD
http://www.LOVD.nl/LONRF3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LPAR4
lysophosphatidic acid receptor 4 300086 |
LPAR4 database at LOVD
http://www.LOVD.nl/LPAR4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LPIN2
lipin 2 605519 |
INFEVERS: The repertory of Familial Mediterranean Fever & Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Hatem El-Shanti, Paediatrics, Jordan University of Science and Technology, Amman, Jordan |
LRAT
lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase) 604863 |
Mutations of the Lecithin Retinol Acyltransferase Gene
http://www.retina-international.org/sci-news/lratmut.htm |
Retina International |
LRCH2
leucine-rich repeats and calponin homology (CH) domain containing 2 |
LRCH2 database at LOVD
http://www.LOVD.nl/LRCH2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LRP5
low density lipoprotein receptor-related protein 5 603506 |
LOVD - Leiden Open Variation Database
http://www.LOVD.nl/LRP5 |
Wim van Hul |
LRRC8A
leucine rich repeat containing 8 family, member A 608360 |
LRRC8Abase: Mutation registry for Non-Bruton type autosomal dominant agammaglobulinemia
http://bioinf.uta.fi/LRRC8Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
LRRK2
leucine-rich repeat kinase 2 609007 |
LRRK2 Parkinson's disease Mutation Database
http://www.LOVD.nl/LRRK2 |
The Parkinson's Institute |
LUZP4
leucine zipper protein 4 300616 |
LUZP4 database at LOVD
http://www.LOVD.nl/LUZP4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
LYST
lysosomal trafficking regulator 606897 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting Int. Albinism Centre Univ. of Minnesota, U.S.A. |
LYST
lysosomal trafficking regulator 606897 |
LYSTbase: Mutation registry for Chediak-Higashi syndrome (previously known as CHS1base)
http://bioinf.uta.fi/LYSTbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
LYST
lysosomal trafficking regulator 606897 |
Mutations of the Chediak Higashi Syndrome
http://www.retina-international.org/sci-news/chsmut.htm |
Retina International |
Go Back To Main Index! | ||
MAF
v-maf musculoaponeurotic fibrosarcoma oncogene homolog (avian) 177075 |
MAF database at LOVD
http://www.LOVD.nl/MAF |
Johan T den Dunnen Leiden Univ. Med Centre |
MAGEA1
melanoma antigen family A, 1 (directs expression of antigen MZ2-E) 300016 |
MAGEA1 database at LOVD
http://www.LOVD.nl/MAGEA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA11
melanoma antigen family A, 11 300344 |
MAGEA11 database at LOVD
http://www.LOVD.nl/MAGEA11 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA12
melanoma antigen family A, 12 300177 |
MAGEA12 database at LOVD
http://www.LOVD.nl/MAGEA12 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA3
melanoma antigen family A, 3 300174 |
MAGEA3 database at LOVD
http://www.LOVD.nl/MAGEA3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA4
melanoma antigen family A, 4 300175 |
MAGEA4 database at LOVD
http://www.LOVD.nl/MAGEA4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA5
melanoma antigen family A, 5 300340 |
MAGEA5 database at LOVD
http://www.LOVD.nl/MAGEA5 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEA8
melanoma antigen family A, 8 300341 |
MAGEA8 database at LOVD
http://www.LOVD.nl/MAGEA8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB1
melanoma antigen family B, 1 300097 |
MAGEB1 database at LOVD
http://www.LOVD.nl/MAGEB1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB10
melanoma antigen family B, 10 300761 |
MAGEB10 database at LOVD
http://www.LOVD.nl/MAGEB10 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB18
melanoma antigen family B, 18 |
MAGEB18 database at LOVD
http://www.LOVD.nl/MAGEB18 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB2
melanoma antigen family B, 2 300098 |
MAGEB2 database at LOVD
http://www.LOVD.nl/MAGEB2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB3
melanoma antigen family B, 3 300152 |
MAGEB3 database at LOVD
http://www.LOVD.nl/MAGEB3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB4
melanoma antigen family B, 4 300153 |
MAGEB4 database at LOVD
http://www.LOVD.nl/MAGEB4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB5
melanoma antigen family B, 5 300466 |
MAGEB5 database at LOVD
http://www.LOVD.nl/MAGEB5 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEB6
melanoma antigen family B, 6 300467 |
MAGEB6 database at LOVD
http://www.LOVD.nl/MAGEB6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEC1
melanoma antigen family C, 1 300223 |
MAGEC1 database at LOVD
http://www.LOVD.nl/MAGEC1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEC2
melanoma antigen family C, 2 300468 |
MAGEC2 database at LOVD
http://www.LOVD.nl/MAGEC2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEC3
melanoma antigen family C, 3 300469 |
MAGEC3 database at LOVD
http://www.LOVD.nl/MAGEC3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGED1
melanoma antigen family D, 1 300224 |
MAGED1 database at LOVD
http://www.LOVD.nl/MAGED1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGED2
melanoma antigen family D, 2 300470 |
MAGED2 database at LOVD
http://www.LOVD.nl/MAGED2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEE1
melanoma antigen family E, 1 300759 |
MAGEE1 database at LOVD
http://www.LOVD.nl/MAGEE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEE2
melanoma antigen family E, 2 300760 |
MAGEE2 database at LOVD
http://www.LOVD.nl/MAGEE2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGEH1
melanoma antigen family H, 1 300548 |
MAGEH1 database at LOVD
http://www.LOVD.nl/MAGEH1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAGT1
magnesium transporter 1 300715 |
MAGT1 database at LOVD
http://www.LOVD.nl/MAGT1 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAMLD1
mastermind-like domain containing 1 300120 |
MAMLD1 database at LOVD
http://www.LOVD.nl/MAMLD1 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAOA
monoamine oxidase A 309850 |
MAOA database at LOVD
http://www.LOVD.nl/MAOA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAOB
monoamine oxidase B 309860 |
MAOB database at LOVD
http://www.LOVD.nl/MAOB |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAP2K1
mitogen-activated protein kinase kinase 1 176872 |
Mitogen-activated protein kinase kinase 1 (MAP2K1) database
http://lovd.bx.psu.edu/home.php?select_db=MAP2K1 |
Belinda Giardine and Joseph Borg |
MAP3K15
mitogen-activated protein kinase kinase kinase 15 |
MAP3K15 database at LOVD
http://www.LOVD.nl/MAP3K15 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAP3K5
mitogen-activated protein kinase kinase kinase 5 602448 |
Mitogen-activated protein kinase kinase kinase 5 (MAP3K5) database
http://lovd.bx.psu.edu/home.php?select_db=MAP3K5 |
Belinda Giardine and Joseph Borg |
MAP3K7
mitogen-activated protein kinase kinase kinase 7 602614 |
Mitogen-activated protein kinase kinase kinase 7 (MAP3K7)
http://lovd.bx.psu.edu/home.php?select_db=MAP3K7 |
Belinda Giardine and Joseph Borg |
MAP7D2
MAP7 domain containing 2 |
MAP7D2 database at LOVD
http://www.LOVD.nl/MAP7D2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAP7D3
MAP7 domain containing 3 |
MAP7D3 database at LOVD
http://www.LOVD.nl/MAP7D3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MAPT
microtubule-associated protein tau 157140 |
Alzheimer Disease & Frontotemporal Dementia Mutation Database
http://www.molgen.ua.ac.be/FTDMutations/ |
Marc Cruts and Nathalie Brouwers, Neurogenerative Brain Diseases Group, VIB Department of Molecular Genetics, Flanders Institute for Biotechnology and, University of Antwerp - Campus CDE, Belgium |
MASP2
mannan-binding lectin serine peptidase 2 605102 |
MASP2base: Mutation registry for MASP-2 deficiency
http://bioinf.uta.fi/MASP2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
MATR3
matrin 3 164015 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/MATR3 |
Johan T den Dunnen Leiden Univ. Med Centre |
MBNL3
muscleblind-like 3 (Drosophila) 300413 |
MBNL3 database at LOVD
http://www.LOVD.nl/MBNL3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MBTPS2
membrane-bound transcription factor peptidase, site 2 300294 |
Membrane-Bound Transcription factor Peptidase, site 2 (MBTPS2) Mental Retardation Database
http://www.LOVD.nl/MBTPS2 |
Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands |
MCEE
methylmalonyl CoA epimerase 608419 |
Zhejiang University Center for Genetic and Genomic Medicine - MCEE
http://www.genomed.org/LOVD/mma/home.php?select_db=MCEE |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MCF2
MCF.2 cell line derived transforming sequence 311030 |
MCF2 database at LOVD
http://www.LOVD.nl/MCF2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MECP2
methyl CpG binding protein 2 (Rett syndrome) 300005 |
RettBASE
http://mecp2.chw.edu.au/ |
John Christodoulou, Andrew Grimm Children's Hospital, Westmead, Sydney, Australia |
MECP2
methyl CpG binding protein 2 (Rett syndrome) 300005 |
MECP2 database at LOVD
http://www.LOVD.nl/MECP2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MECP2
methyl CpG binding protein 2 (Rett syndrome) 300005 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=MECP2 |
Ammar Husami and Theru A. Sivakumaran |
MED12
mediator complex subunit 12 300188 |
MED12 database at LOVD
http://www.LOVD.nl/MED12 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MED14
mediator complex subunit 14 300182 |
MED14 database at LOVD
http://www.LOVD.nl/MED14 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MEFV
Mediterranean fever 608107 |
INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Isabelle Touitou, Laboratory of Genetics, A de Villeneuve Hospital, Montpellier, France |
MEN1
multiple endocrine neoplasia I 131100 |
The UMD MEN1 mutations database
http://www.umd.be/MEN1/ |
Alain Calender, Genetic Unit and INSERM U45, H�pital Edouard Herriot, LYON, France |
MERTK
c-mer proto-oncogene tyrosine kinase 604705 |
Mutations of the MER Receptor Tyrosine Kinase Gene
http://www.retina-international.org/sci-news/mertkmut.htm |
Retina International |
MFN2
mitofusin 2 608507 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB, University of Antwerp (UA), Belgium |
MFSD8
major facilitator superfamily domain containing 8 611124 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
MGAT2
mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase 602616 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics, Leuven, Belgium |
MICA
MHC class I polypeptide-related sequence A 600169 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
MICB
MHC class I polypeptide-related sequence B 602436 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
MID1
midline 1 (Opitz/BBB syndrome) 300552 |
MID1 database at LOVD
http://www.LOVD.nl/MID1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MID2
midline 2 300204 |
MID2 database at LOVD
http://www.LOVD.nl/MID2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MITF
microphthalmia-associated transcription factor 156845 |
MITF database at LOVD
http://www.LOVD.nl/MITF |
Veronique Pingault Laboratoire de Biochimie et G�n�tique, Hopital Henri Mondor Creteil cedex, France |
MKKS
McKusick-Kaufman syndrome 604896 |
Mutations of the McKusick-Kaufman Gene
http://www.retina-international.org/sci-news/mkksmut.htm |
Retina International |
MLH1
mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) 120436 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC): Amanda Dohey, Hans Vasen, Krista Mahoney, Michael Woods, Paivi Peltom�ki and Rolf Sijmons |
MLH1
mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) 120436 |
Mismatch Repair Genes Variant Database
http://www.med.mun.ca/mmrvariants/ |
Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, Canada |
MLH1
mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) 120436 |
Zhejiang University-Adinovo Center MLH1 Database
http://www.china-hvp.org/LOVD/?select_db=MLH1 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
MLH3
mutL homolog 3 (E. coli) 604395 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC) |
MLH3
mutL homolog 3 (E. coli) 604395 |
Zhejiang University-Adinovo Center MLH3 Database
http://www.china-hvp.org/LOVD/?select_db=MLH3 |
Ming Qi, PhD, FACMG, Peikuan Cong, Shu Zheng, MD, Yudong Gao and Changsong Lin |
MLPH
melanophilin 606526 |
MLPHbase: Mutation registry for Griscelli syndrome, type 3 (GS3)
http://bioinf.uta.fi/MLPHbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
MLYCD
malonyl-CoA decarboxylase 606761 |
MLYCD Allelic Variant Database
http://mlycd.hgu.mrc.ac.uk/ |
Graeme Grimes & Isabel Hanson, MRC Human Genetics Unit, Edinburg, UK |
MMAA
methylmalonic aciduria (cobalamin deficiency) cblA type 607481 |
Zhejiang University Center for Genetic and Genomic Medicine - MMAA
http://www.genomed.org/LOVD/mma/home.php?select_db=MMAA |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MMAB
methylmalonic aciduria (cobalamin deficiency) cblB type 607568 |
Zhejiang University Center for Genetic and Genomic Medicine - MMAB
http://www.genomed.org/LOVD/mma/home.php?select_db=MMAB |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MMACHC
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria 609831 |
Zhejiang University Center for Genetic and Genomic Medicine - MMACHC
http://www.china-hvp.org/LOVD/?select_db=MMACHC |
Ming Qi, PhD, FACMG |
MMADHC
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria 611935 |
Zhejiang University Center for Genetic and Genomic Medicine - MMADHC
http://www.genomed.org/LOVD/mma/home.php?select_db=MMADHC |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MOGS
mannosyl-oligosaccharide glucosidase 601336 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics, Leuven, Belgium |
MORC4
MORC family CW-type zinc finger 4 |
MORC4 database at LOVD
http://www.LOVD.nl/MORC4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MOSPD2
motile sperm domain containing 2 |
MOSPD2 database at LOVD
http://www.LOVD.nl/MOSPD2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MPDU1
mannose-P-dolichol utilization defect 1 604041 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
MPI
mannose phosphate isomerase 154550 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics, Leuven, Belgium |
MPO
myeloperoxidase 606989 |
MPObase: Mutation registry for Myeloperoxidase deficiency
http://bioinf.uta.fi/MPObase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
MPP1
membrane protein, palmitoylated 1, 55kDa 305360 |
MPP1 database at LOVD
http://www.LOVD.nl/MPP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MPZ
myelin protein zero 159440 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
MRE11A
MRE11 meiotic recombination 11 homolog A (S. cerevisiae) 600814 |
MRE11Abase: Mutation registry for Ataxia-telangiectasia-like disorder (ATLD)
http://bioinf.uta.fi/MRE11Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
MSH2
mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) 609309 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC): Amanda Dohey, Hans Vasen, Krista Mahoney, Michael Woods, Paivi Peltom�ki and Rolf Sijmons |
MSH2
mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) 609309 |
Mismatch Repair Genes Variant Database
http://www.med.mun.ca/mmrvariants/ |
Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, Canada |
MSH2
mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) 609309 |
Zhejiang University-Adinovo Center MSH2 Database
http://www.china-hvp.org/LOVD/?select_db=MSH2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Shu Zheng, MD, Yudong Gao and Changsong Lin |
MSH6
mutS homolog 6 (E. coli) 600678 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC) |
MSH6
mutS homolog 6 (E. coli) 600678 |
Mismatch Repair Genes Variant Database
http://www.med.mun.ca/mmrvariants/ |
Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, Canada |
MSH6
mutS homolog 6 (E. coli) 600678 |
MSH6 database at LOVD
http://www.LOVD.nl/MSH6 |
Amanda Dohey & Michael Woods, Memorial University of Newfoundland, Canada |
MSH6
mutS homolog 6 (E. coli) 600678 |
Zhejiang University-Adinovo Center MSH6 Database
http://www.china-hvp.org/LOVD/?select_db=MSH6 |
Ming Qi, PhD, FACMG, Peikuan Cong, Shu Zheng, MD, Yudong Gao and Changsong Lin |
MSL3
male-specific lethal 3 homolog (Drosophila) 300609 |
MSL3 database at LOVD
http://www.LOVD.nl/MSL3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MSN
moesin 309845 |
MSN database at LOVD
http://www.LOVD.nl/MSN |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MSTN
myostatin 601788 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/MSTN |
Willem Hoogaars & Johan den Dunnen |
MT-TS2
mitochondrially encoded tRNA serine 2 (AGU/C) 590085 |
Mutations of the Second Mitochondrial Serine tRNA Gene
http://www.retina-international.org/sci-news/mttsmut.htm |
Retina International |
MTM1
myotubularin 1 300415 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/MTM1 |
Jorge Oliveira & Johan den Dunnen |
MTMR1
myotubularin related protein 1 300171 |
MTMR1 database at LOVD
http://www.LOVD.nl/MTMR1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MTMR14
myotubularin related protein 14 611089 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/MTMR14 |
Johan T den Dunnen Leiden Univ. Med Centre |
MTMR2
myotubularin related protein 2 603557 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
MTMR8
myotubularin related protein 8 |
MTMR8 database at LOVD
http://www.LOVD.nl/MTMR8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MTR
5-methyltetrahydrofolate-homocysteine methyltransferase 156570 |
Zhejiang University Center for Genetic and Genomic Medicine - MTR
http://www.genomed.org/LOVD/mma/home.php?select_db=MTR |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MTRR
5-methyltetrahydrofolate-homocysteine methyltransferase reductase 602568 |
Zhejiang University Center for Genetic and Genomic Medicine - MTRR
http://www.genomed.org/lovd/mma/home.php?select_db=MTRR |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MUM1L1
melanoma associated antigen (mutated) 1-like 1 |
MUM1L1 database at LOVD
http://www.LOVD.nl/MUM1L1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MUT
methylmalonyl CoA mutase 609058 |
Zhejiang University Center for Genetic and Genomic Medicine - MUT
http://www.genomed.org/lovd/mma/home.php?select_db=MUT |
Ming Qi, PhD, FACMG, Peikuan Cong and Yanling Chen |
MUTYH
mutY homolog (E. coli) 604933 |
MUTYH - mutY homolog
http://www.LOVD.nl/MUTYH |
Astrid Out & Carli Tops, LUMC, Leiden, Nederland |
MVK
mevalonate kinase 251170 |
INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Laurence Cuisset & Hans Waterham, G�n�tique D�veloppement et Pathologie Mol�culaire, Institut Cochin de G�n�tique Mol�culaire, Paris, France |
MXRA5
matrix-remodelling associated 5 |
MXRA5 database at LOVD
http://www.LOVD.nl/MXRA5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
MYB
v-myb myeloblastosis viral oncogene homolog (avian) 189990 |
Homo sapiens v-myb myeloblastosis viral oncogene homolog (MYB) database
http://lovd.bx.psu.edu/home.php?select_db=MYB |
Belinda Giardine and Joseph Borg |
MYBPC3
myosin binding protein C, cardiac 600958 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Molecular & Clinical Genetics, Royal Prince Alfred Hospital, Sydney, Australia |
MYBPC3
myosin binding protein C, cardiac 600958 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/MYBPC3_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School |
MYH7
myosin, heavy chain 7, cardiac muscle, beta 160760 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Molecular & Clinical Genetics, Royal Prince Alfred Hospital, Sydney, Australia |
MYH7
myosin, heavy chain 7, cardiac muscle, beta 160760 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/MYH7_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
MYH9
myosin, heavy chain 9, non-muscle 160775 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium, Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
MYL2
myosin, light chain 2, regulatory, cardiac, slow 160781 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Molecular & Clinical Genetics, Royal Prince Alfred Hospital, Sydney, Australia |
MYL2
myosin, light chain 2, regulatory, cardiac, slow 160781 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/MYL2_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
MYL3
myosin, light chain 3, alkali; ventricular, skeletal, slow 160790 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/MYL3_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
MYO15A
myosin XVA 602666 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
MYO5A
myosin VA (heavy chain 12, myoxin) 160777 |
MYO5Abase: Mutation registry for Griscelli syndrome, type 1 (GS1)
http://bioinf.uta.fi/MYO5Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
MYO6
myosin VI 600970 |
Hereditary Hearing Loss Homepage
http://hereditaryhearingloss.org/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
MYO6
myosin VI 600970 |
CCHMC-BMI & UC Hearing Loss Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=MYO6 |
Ammar Husami |
MYO7A
myosin VIIA 276903 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
MYO7A
myosin VIIA 276903 |
Mutations of the Myosin VIIa Gene
http://www.retina-international.org/sci-news/myomut.htm |
Retina International |
MYO7A
myosin VIIA 276903 |
The UMD MYO7A mutations database
http://www.umd.be/MYO7A/ |
A.-F. Roux and D. Baux |
MYO7A
myosin VIIA 276903 |
Retinal and hearing impairment genetic mutation database MYO7A
http://www.LOVD.nl/MYO7A |
david baux |
MYO7A
myosin VIIA 276903 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=MYO7A |
Ammar Husami and Theru A. Sivakumaran |
MYOC
myocilin, trabecular meshwork inducible glucocorticoid response 601652 |
Myocilin allele-specific phenotype database
http://www.myocilin.com/ |
Dr Alex Hewitt & A/Prof Jamie Craig, Department of Ophthalmology, Flinders University, Adelaide, Australia. |
MYOT
myotilin 604103 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/MYOT |
Johan den Dunnen |
Go Back To Main Index! | ||
NAGS
N-acetylglutamate synthase 608300 |
NAGS database at LOVD
http://www.LOVD.nl/NAGS |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NAP1L2
nucleosome assembly protein 1-like 2 300026 |
NAP1L2 database at LOVD
http://www.LOVD.nl/NAP1L2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NAP1L3
nucleosome assembly protein 1-like 3 300117 |
NAP1L3 database at LOVD
http://www.LOVD.nl/NAP1L3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NAP1L6
nucleosome assembly protein 1-like 6 |
NAP1L6 database at LOVD
http://www.LOVD.nl/NAP1L6 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NAT1
N-acetyltransferase 1 (arylamine N-acetyltransferase) 108345 |
Arylamine N-Acetyltransferase(Note- Not really a variation database but useful-lists alleles & nomenclature)
http://louisville.edu/medschool/pharmacology/NAT.html |
David W. Hein, Dept Pharmacology & Toxicology Univ. Sch. Med. Louisville, Kentucky USA; Denis M. Grant, The Hospital for Sick Children, Toronto Canada; Edith Sim, Dept Pharmacology Univ. Oxford, UK |
NAT2
N-acetyltransferase 2 (arylamine N-acetyltransferase) 612182 |
Arylamine N-Acetyltransferase (Note- Not really a variation database but useful-lists alleles & nomenclature)
http://louisville.edu/medschool/pharmacology/NAT.html |
David W. Hein, Dept Pharmacology & Toxicology, Univ. Sch. Med. Louisville, Kentucky, USA; Denis M. Grant, The Hospital for Sick Children, Toronto, Canada; Edith Sim, Dept Pharmacology, Univ. Oxford, UK |
NBN
nibrin 602667 |
NBN - Leiden Open Variation Database
http://www.LOVD.nl/NBN |
Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy |
NCBP2L
nuclear cap binding protein subunit 2-like |
NCBP2L database at LOVD
http://www.LOVD.nl/NCBP2L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NCF1
neutrophil cytosolic factor 1 608512 |
NCF1base: Mutation registry for autosomal recessive chronic granulomatous disease (CGD), deficiency of p47phox
http://bioinf.uta.fi/NCF1base/ |
Dirk Roos, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
NCF2
neutrophil cytosolic factor 2 608515 |
NCF2base: Mutation registry for autosomal recessive chronic granulomatous disease (CGD), deficiency of p67phox
http://bioinf.uta.fi/NCF2base/ |
Dirk Roos, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
NCRNA00105
non-protein coding RNA 105 |
NCRNA00105 database at LOVD
http://www.LOVD.nl/NCRNA00105 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NCRNA00236
non-protein coding RNA 236 |
CXorf25 database at LOVD
http://www.LOVD.nl/CXorf25 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NDP
Norrie disease (pseudoglioma) 300658 |
Mutations of the Norrie Disease Gene
http://www.retina-international.org/sci-news/ndgmut.htm |
Retina International |
NDRG1
N-myc downstream regulated 1 605262 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
NDUFA1
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kDa 300078 |
NDUFA1 database at LOVD
http://www.LOVD.nl/NDUFA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NEB
nebulin 161650 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/NEB |
Katarina Pelin, Tom Winder, Vilma-Lotta Lehtokari & Johan den Dunnen |
NEFL
neurofilament, light polypeptide 162280 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics, Department, Flanders Interuniversity, Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
NF1
neurofibromin 1 162200 |
NF1 @ The Center for Medical Genetics, Ghent University Hospital, Belgium
http://medgen.ugent.be/LOVD2/ |
Ophelia Maertens, Centre for Medical Genetics Gent, Belgium |
NFKBIA
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha 164008 |
NFKBIAbase: Mutation registry for Autosomal dominant anhidrotic ectodermal dysplasia and T-cell immunodeficiency
http://bioinf.uta.fi/NFKBIAbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
NGF
nerve growth factor (beta polypeptide) 162030 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
NHEJ1
nonhomologous end-joining factor 1 611290 |
NHEJ1base: Mutation registry for Combined immunodeficiency (CID) associated with microcephaly and increased cellular sensitivity to IR
http://bioinf.uta.fi/NHEJ1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
NHP2
NHP2 ribonucleoprotein homolog (yeast) 606470 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#nola2 |
Julian J-L Chen at Arizona State University |
NHS
Nance-Horan syndrome (congenital cataracts and dental anomalies) 300457 |
NHS database at LOVD
http://www.LOVD.nl/NHS |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NHSL2
NHS-like 2 |
NHSL2 database at LOVD
http://www.LOVD.nl/NHSL2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NIPBL
Nipped-B homolog (Drosophila) 608667 |
NIPBL - LOVD
http://www.LOVD.nl/NIPBL |
Jorge Oliveira, Unidade de Gen�tica Molecular, Centro de Gen�tica M�dica J. Magalh�es - INSA, Porto, Portugal; Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
NKAP
NFKB activating protein 300766 |
NKAP database at LOVD
http://www.LOVD.nl/NKAP |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NKRF
NFKB repressing factor 300440 |
NKRF database at LOVD
http://www.LOVD.nl/NKRF |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NLGN3
neuroligin 3 300336 |
NLGN3 database at LOVD
http://www.LOVD.nl/NLGN3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NLGN4X
neuroligin 4, X-linked 300427 |
NLGN4X database at LOVD
http://www.LOVD.nl/NLGN4X |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NLRP3
NLR family, pyrin domain containing 3 606416 |
INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Hal Hoffmann, Medicine and Pediatrics, University of California at San Diego, La Jolla,USA |
NLRP7
NLR family, pyrin domain containing 7 609661 |
INFEVERS: The repertory of RMHs sequence variants
http://fmf.igh.cnrs.fr/infevers/ |
Rima Slim, Montreal General Hospital Research Institute, Montreal, Canada |
NOD2
nucleotide-binding oligomerization domain containing 2 605956 |
Crohn's Disease & Blau Syndrome; INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Jean-pierre Hugot & Suzanne Lesage, INSERM 289, Paris, France |
NOG
noggin 602991 |
Sequence alterations in the NOG gene
http://www.LOVD.nl/NOG |
Sarah Emery |
NOP10
NOP10 ribonucleoprotein homolog (yeast) 606471 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#nola3 |
Julian J-L Chen at Arizona State University |
NOS1
nitric oxide synthase 1 (neuronal) 163731 |
Nitric oxide synthase 1 (neuronal) (NOS1) database
http://lovd.bx.psu.edu/home.php?select_db=NOS1 |
Belinda Giardine and Joseph Borg |
NOS2
nitric oxide synthase 2, inducible 163730 |
Nitric oxide synthase 2, inducible (NOS2A) database
http://lovd.bx.psu.edu/home.php?select_db=NOS2A |
Belinda Giardine and Joseph Borg |
NOS3
nitric oxide synthase 3 (endothelial cell) 163729 |
Nitric oxide synthase 3 (endothelial cell) (NOS3) database
http://lovd.bx.psu.edu/home.php?select_db=NOS3 |
Belinda Giardine and Joseph Borg |
NOTCH3
Notch homolog 3 (Drosophila) 600276 |
NOTCH3 - CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical
http://www.LOVD.nl/NOTCH3 |
Elles Boon, LUMC, Leiden, Nederland |
NOX1
NADPH oxidase 1 300225 |
NOX1 database at LOVD
http://www.LOVD.nl/NOX1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NOX3
NADPH oxidase 3 607105 |
NADPH oxidase 3 (NOX3) database
http://lovd.bx.psu.edu/home.php?select_db=NOX3 |
Belinda Giardine and Joseph Borg |
NR0B1
nuclear receptor subfamily 0, group B, member 1 300473 |
NROB1 - adrenal hypoplasia (DAX1)
http://www.LOVD.nl/NROB1 |
Bert Bakker, LUMC, Leiden, Nederland |
NR2E3
nuclear receptor subfamily 2, group E, member 3 604485 |
Mutations of the Photoreceptor cell-specific Nuclear Receptor
http://www.retina-international.org/sci-news/nr2e3mut.htm |
Retina International |
NR2E3
nuclear receptor subfamily 2, group E, member 3 604485 |
NR2E3 database at LOVD
http://www.LOVD.nl/NR2E3 |
Pascal Escher, IRO-Institut de Recherche en Ophtalmologie, Switzerland |
NR3C1
nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 138040 |
Glucocorticoid Receptor Resource database
http://nrr.georgetown.edu/GRR/mutation/mutation.html |
S.Stoney Simons, Mark Danielsen, Georgetown Univ. Georgetown, USA |
NRK
Nik related kinase 300791 |
NRK database at LOVD
http://www.LOVD.nl/NRK |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NRL
neural retina leucine zipper 162080 |
Mutations of the Neuroretina-linked Leucine Zipper Gene
http://www.retina-international.org/sci-news/nrlmut.htm |
Retina International |
NSD1
nuclear receptor binding SET domain protein 1 606681 |
NSD1 at LOVD
http://www.LOVD.nl/NSD1 |
Janneke Weiss, LUMC, Leiden, Netherlands |
NSDHL
NAD(P) dependent steroid dehydrogenase-like 300275 |
NSDHL database at LOVD
http://www.LOVD.nl/NSDHL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NTRK1
neurotrophic tyrosine kinase, receptor, type 1 191315 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
NUP133
nucleoporin 133kDa 607613 |
Nucleoporin 133kDa (NUP133) database
http://lovd.bx.psu.edu/home.php?select_db=NUP133 |
Belinda Giardine and Joseph Borg |
NUP62CL
nucleoporin 62kDa C-terminal like |
NUP62CL database at LOVD
http://www.LOVD.nl/NUP62CL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NXF3
nuclear RNA export factor 3 300316 |
NXF3 database at LOVD
http://www.LOVD.nl/NXF3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NXF5
nuclear RNA export factor 5 300319 |
NXF5 database at LOVD
http://www.LOVD.nl/NXF5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
NYX
nyctalopin 300278 |
Mutations of Nyctalopin
http://www.retina-international.org/sci-news/nyxmut.htm |
Retina International |
Go Back To Main Index! | ||
OCA2
oculocutaneous albinism II 611409 |
Mutations of the P-Gene
http://www.retina-international.org/sci-news/pgenemut.htm |
Retina International |
OCA2
oculocutaneous albinism II 611409 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota, U.S.A. |
OCRL
oculocerebrorenal syndrome of Lowe 300535 |
Database of the OCRL1 Mutations Causing Lowe Syndrome
http://research.nhgri.nih.gov/lowe/ |
Robert L. Nussbaum, Sharon F. Suchy, Ti Lin, Genetic Disease Research Branch, NHGRI/NIH Bethesda, USA |
ODZ1
odz, odd Oz/ten-m homolog 1(Drosophila) 300588 |
ODZ1 database at LOVD
http://www.LOVD.nl/ODZ1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
OFD1
oral-facial-digital syndrome 1 300170 |
OFD1 database at LOVD
http://www.LOVD.nl/OFD1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
OGT
O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase) 300255 |
OGT database at LOVD
http://www.LOVD.nl/OGT |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
OPA1
optic atrophy 1 (autosomal dominant) 605290 |
Mutations of the Optic Atrophy 1 Gene
http://www.retina-international.org/sci-news/opa1mut.htm |
Retina International |
OPA1
optic atrophy 1 (autosomal dominant) 605290 |
eOPA1
http://lbbma.univ-angers.fr/lbbma.php?id=9 |
Patrizia Bonneau, CHU Angers - Inserm, Departement de Biochimie et Genetique, France |
OPHN1
oligophrenin 1 300127 |
OPHN1 database at LOVD
http://www.LOVD.nl/OPHN1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
OPN1LW
opsin 1 (cone pigments), long-wave-sensitive 303900 |
Mutations of the Photopigments - Red (RCP), Green (GCP), and Blue Cone Pigment (BCP)
http://www.retina-international.org/sci-news/cppmut.htm |
Retina International |
OPN1MW
opsin 1 (cone pigments), medium-wave-sensitive 303800 |
Mutations of the Photopigments - Red (RCP), Green (GCP), and Blue Cone Pigment (BCP)
http://www.retina-international.org/sci-news/cppmut.htm |
Retina International |
OPN1SW
opsin 1 (cone pigments), short-wave-sensitive 190900 |
Mutations of the Photopigments - Red (RCP), Green (GCP), and Blue Cone Pigment (BCP)
http://www.retina-international.org/sci-news/cppmut.htm |
Retina International |
OTC
ornithine carbamoyltransferase 300461 |
Ornithine Transcarbamylase Deficiency Website
http://ureacycle.cnmcresearch.org/otc/ |
Hiroki Morizono, Mendel Tuchman, Children's National Medical Center, Washington DC, USA |
OTC
ornithine carbamoyltransferase 300461 |
OTC - Ornithine transcarbamylase deficiency
http://www.LOVD.nl/OTC |
Bert Bakker, LUMC, Leiden, Nederland |
OTOF
otoferlin 603681 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
OTOF
otoferlin 603681 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=OTOF |
Ammar Husami and Theru A. Sivakumaran |
OTX2
orthodenticle homeobox 2 600037 |
OTX2 Allelic Variant Database
http://lsdb.hgu.mrc.ac.uk/home.php?select_db=OTX2 |
Graeme Grimes, Isabel Hanson, David FitzPatrick, Kathy Williamson and Veronica van Heyningen |
Go Back To Main Index! | ||
P2RY10
purinergic receptor P2Y, G-protein coupled, 10 300529 |
P2RY10 database at LOVD
http://www.LOVD.nl/P2RY10 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
P2RY4
pyrimidinergic receptor P2Y, G-protein coupled, 4 300038 |
P2RY4 database at LOVD
http://www.LOVD.nl/P2RY4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
P2RY8
purinergic receptor P2Y, G-protein coupled, 8 300525 |
P2RY8 database at LOVD
http://www.LOVD.nl/P2RY8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PABPC5
poly(A) binding protein, cytoplasmic 5 300407 |
PABPC5 database at LOVD
http://www.LOVD.nl/PABPC5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PABPN1
poly(A) binding protein, nuclear 1 602279 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/PABPN1 |
Johan T den Dunnen Leiden Univ. Med Centre |
PAGE1
P antigen family, member 1 (prostate associated) 300288 |
PAGE1 database at LOVD
http://www.LOVD.nl/PAGE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PAGE3
P antigen family, member 3 (prostate associated) 300739 |
PAGE3 database at LOVD
http://www.LOVD.nl/PAGE3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PAH
phenylalanine hydroxylase 612349 |
Phenylalanine Hydroxylase Locus Knowledgebase
http://www.pahdb.mcgill.ca |
Charles R. Scriver, Lynne Prevost, M�lanie Hurtubise & David Konecki, PAH Mutation Analysis Consortium, McGill University, Montreal, Canada |
PALB2
partner and localizer of BRCA2 610355 |
Fanconi Anaemia Mutation Database
http://www.rockefeller.edu/fanconi/mutate/ |
Arleen Auerbach, Rockefeller University, New York, USA |
PARK2
Parkinson disease (autosomal recessive, juvenile) 2, parkin 602544 |
PARK2 Parkinson's disease Mutation Database
http://www.LOVD.nl/PARK2 |
The Parkinson's Institute |
PARK7
Parkinson disease (autosomal recessive, early onset) 7 602533 |
PARK7 Parkinson's disease Mutation Database
http://www.LOVD.nl/PARK7 |
The Parkinson's Institute |
PASD1
PAS domain containing 1 |
PASD1 database at LOVD
http://www.LOVD.nl/PASD1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PAX2
paired box 2 167409 |
PAX2 Mutation Database
http://pax2.hgu.mrc.ac.uk/ |
Graeme Grimes & Isabel Hanson, MRC, Human Genetics Unit, Edinburgh, UK |
PAX3
paired box 3 606597 |
PAX3 database at LOVD
http://www.LOVD.nl/PAX3 |
Veronique Pingault Laboratoire de Biochimie et G�n�tique, Hopital Henri Mondor Creteil cedex, France |
PAX6
paired box 6 607108 |
PAX6 Mutation Database-Aniridia Type II
http://pax6.hgu.mrc.ac.uk/ |
Graeme Grimes & Isabel Hanson MRC, Human Genetics Unit Edinburgh, UK |
PCBD1
pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha 126090 |
Pterin-4a-carbionolaminedehydratase deficiency-BIOMED database
http://www.bh4.org/ |
N. Blau, Univ.Children's Hospital, Zurich J.L. Dhont, Facult�libre de M�dicine, Lille, I.Dianzani, Univ.Torino, Torino, Italy |
PCBD1
pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha 126090 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Univ.Children's Hospital, Zurich |
PCCA
propionyl Coenzyme A carboxylase, alpha polypeptide 232000 |
Propionyl CoA Carboxylase Page
http://www.uchsc.edu/cbs/pcc/pccmain.htm |
Jan P. Kraus, Maja Chloupkova, Dept. Paediatrics, Univ. of Colorado, Sch. Of Med. Denver, USA, Mirek Janosik, Inst. Inherited Metabolic Dis., 1st Fac. Of Med., Charles Univ. Prague, Czech Rep. |
PCCB
propionyl Coenzyme A carboxylase, beta polypeptide 232050 |
Propionyl CoA Carboxylase Page
http://www.uchsc.edu/cbs/pcc/pccmain.htm |
Jan P. Kraus, Maja Chloupkova, Dept. Paediatrics, Univ. of Colorado, Sch. Of Med. Denver, USA, Mirek Janosik, Inst. Inherited Metabolic Dis., 1st Fac. Of Med., Charles Univ. Prague, Czech Rep. |
PCDH11X
protocadherin 11 X-linked 300246 |
PCDH11X database at LOVD
http://www.LOVD.nl/PCDH11X |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PCDH15
protocadherin-related 15 605514 |
Mutations of the Protocadherin 15 Gene
http://www.retina-international.org/sci-news/pcdhmut.htm |
Retina International |
PCDH15
protocadherin-related 15 605514 |
The UMD PCDH15 mutations database
http://www.umd.be/PCDH15/ |
A.-F. Roux and D. Baux |
PCDH15
protocadherin-related 15 605514 |
Retinal and hearing impairment genetic mutation database PCDH15
http://www.LOVD.nl/PCDH15 |
david baux |
PCDH15
protocadherin-related 15 605514 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=PCDH15 |
Ammar Husami and Theru A. Sivakumaran |
PCDH19
protocadherin 19 300460 |
PCDH19 database at LOVD
http://www.LOVD.nl/PCDH19 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PCNT
pericentrin 605925 |
Mental Retardation database - pericentrin (PCNT)
http://www.LOVD.nl/PCNT |
Johan T den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PCSK9
proprotein convertase subtilisin/kexin type 9 607786 |
Hypercholesterolemia, Familial
http://www.ucl.ac.uk/ldlr/LOVDv.1.1.0/ |
Sarah Leigh |
PCYT1B
phosphate cytidylyltransferase 1, choline, beta 604926 |
PCYT1B database at LOVD
http://www.LOVD.nl/PCYT1B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PDC
phosducin 171490 |
Mutations of the Phosducin Gene
http://www.retina-international.org/sci-news/pdcmut.htm |
Retina International |
PDE6A
phosphodiesterase 6A, cGMP-specific, rod, alpha 180071 |
Mutations of the Phosphodiesterase type 6
http://www.retina-international.org/sci-news/pdemut.htm |
Retina International |
PDE7B
phosphodiesterase 7B 604645 |
Phosphodiesterase 7B (PDE7B) database
http://lovd.bx.psu.edu/home.php?select_db=PDE7B |
Belinda Giardine and Joseph Borg |
PDHA1
pyruvate dehydrogenase (lipoamide) alpha 1 300502 |
PDHA1 database at LOVD
http://www.LOVD.nl/PDHA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PDK3
pyruvate dehydrogenase kinase, isozyme 3 602526 |
PDK3 database at LOVD
http://www.LOVD.nl/PDK3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PDS5A
PDS5, regulator of cohesion maintenance, homolog A (S. cerevisiae) 613200 |
PDS5A database at LOVD
http://www.LOVD.nl/PDS5A |
Johan T den Dunnen Leiden Univ. Med Centre |
PDS5B
PDS5, regulator of cohesion maintenance, homolog B (S. cerevisiae) 605333 |
PDS5B database at LOVD
http://grenada.lumc.nl/LOVD2/CDLS/home.php?select_db=PDS5B |
Johan T den Dunnen Leiden Univ. Med Centre |
PEX1
peroxisomal biogenesis factor 1 602136 |
dbPEX, PEX1 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX10
peroxisomal biogenesis factor 10 602859 |
dbPEX, PEX10 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX12
peroxisomal biogenesis factor 12 601758 |
dbPEX, PEX12 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX13
peroxisomal biogenesis factor 13 601789 |
dbPEX, PEX13 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX14
peroxisomal biogenesis factor 14 601791 |
dbPEX, PEX14 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX16
peroxisomal biogenesis factor 16 603360 |
dbPEX, PEX16 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX19
peroxisomal biogenesis factor 19 600279 |
dbPEX, PEX19 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX2
peroxisomal biogenesis factor 2 170993 |
dbPEX, PEX2 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX26
peroxisomal biogenesis factor 26 608666 |
dbPEX, PEX26 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX3
peroxisomal biogenesis factor 3 603164 |
dbPEX, PEX3 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX5
peroxisomal biogenesis factor 5 600414 |
dbPEX, PEX5 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX6
peroxisomal biogenesis factor 6 601498 |
dbPEX, PEX6 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PEX7
peroxisomal biogenesis factor 7 601757 |
dbPEX, PEX7 Gene Database
http://www.dbpex.org/ |
Nancy Braverman and Steven Steinberg, The Johns Hopkins Medical Institutions and Kennedy Krieger Institute, Baltimore MD, USA. |
PFKFB1
6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 311790 |
PFKFB1 database at LOVD
http://www.LOVD.nl/PFKFB1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PGAM4
phosphoglycerate mutase family member 4 300567 |
PGAM4 database at LOVD
http://www.LOVD.nl/PGAM4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PGK1
phosphoglycerate kinase 1 311800 |
PGK1 database at LOVD
http://www.LOVD.nl/PGK1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PGRMC1
progesterone receptor membrane component 1 300435 |
PGRMC1 database at LOVD
http://www.LOVD.nl/PGRMC1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PHEX
phosphate regulating endopeptidase homolog, X-linked 300550 |
PHEXdb Locus Database
http://www.phexdb.mcgill.ca |
Y. Sabbagh, A. O. Jones, H. S. Tenenhouse, Manyphong Phommarinh, McGill University , Canada, Montreal |
PHF16
PHD finger protein 16 300618 |
PHF16 database at LOVD
http://www.LOVD.nl/PHF16 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PHF8
PHD finger protein 8 300560 |
PHF8 database at LOVD
http://www.LOVD.nl/PHF8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PHKA1
phosphorylase kinase, alpha 1 (muscle) 311870 |
PHKA1 database at LOVD
http://www.LOVD.nl/PHKA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PHKA2
phosphorylase kinase, alpha 2 (liver) 306000 |
PHKA2 database at LOVD
http://www.LOVD.nl/PHKA2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PIGA
phosphatidylinositol glycan anchor biosynthesis, class A 311770 |
PIGA database at LOVD
http://www.LOVD.nl/PIGA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PIM2
pim-2 oncogene 300295 |
PIM2 database at LOVD
http://www.LOVD.nl/PIM2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PIN4
protein (peptidylprolyl cis/trans isomerase) NIMA-interacting, 4 (parvulin) 300252 |
PIN4 database at LOVD
http://www.LOVD.nl/PIN4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PINK1
PTEN induced putative kinase 1 608309 |
PINK1 Parkinson's disease Mutation Database
http://www.LOVD.nl/PINK1 |
The Parkinson's Institute |
PIR
pirin (iron-binding nuclear protein) 603329 |
PIR database at LOVD
http://www.LOVD.nl/PIR |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PITX3
paired-like homeodomain 3 602669 |
PITX3 database at LOVD
http://www.LOVD.nl/PITX3 |
Johan T den Dunnen Leiden Univ. Med Centre |
PJA1
praja ring finger 1 300420 |
PJA1 database at LOVD
http://www.LOVD.nl/PJA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PKD1
polycystic kidney disease 1 (autosomal dominant) 601313 |
Autosomal Dominant Polycystic Kidney Disease: Mutation Database
http://pkdb.mayo.edu/ |
Polycystic Kidney Research Foundation |
PKD1
polycystic kidney disease 1 (autosomal dominant) 601313 |
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
http://www.LOVD.nl/PKD1 |
Dr. Francesco Caruso, Dr. Riccardo Magistroni, Dr. Daniele Lodi, Dr.ssa Lucia Palmieri and Dr.ssa Paola Carrera |
PKD2
polycystic kidney disease 2 (autosomal dominant) 173910 |
Autosomal Dominant Polycystic Kidney Disease: Mutation Database
http://pkdb.mayo.edu/ |
Polycystic Kidney Research Foundation |
PKD2
polycystic kidney disease 2 (autosomal dominant) 173910 |
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
http://www.LOVD.nl/PKD2 |
Dr. Francesco Caruso, Dr. Riccardo Magistroni, Dr. Daniele Lodi, Dr.ssa Lucia Palmieri and Dr.ssa Paola Carrera |
PKHD1
polycystic kidney and hepatic disease 1 (autosomal recessive) 606702 |
Autosomal Recessive Polycystic Kidney Disease
http://www.humgen.rwth-aachen.de/ |
Carsten Bergmann, Klaus Zerres, Dept. of Human Genetics, Aachen University, Aachen Germany |
PKLR
pyruvate kinase, liver and RBC 609712 |
PKLR Mutation Database
http://www.pklrmutationdatabase.com/ |
Richard van Wijk, University Medical Center Utrecht, Utrecht, The Netherlands |
PKP2
plakophilin 2 602861 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
PKP2
plakophilin 2 602861 |
ARVD/C Genetic Variants Database
http://www.LOVD.nl/PKP2 |
Paul van der Zwaag |
PLA2G6
phospholipase A2, group VI (cytosolic, calcium-independent) 603604 |
Mutation Database for Phospholipase A2 GroupVI - Associated Neurodegeneration (PLAN)
http://grenada.lumc.nl/LOVD2/shared1/home.php?select_db=PLA2G6 |
Dr Manju A Kurian, Ms Danielle Crompton, and Dr Derek Lim |
PLCXD1
phosphatidylinositol-specific phospholipase C, X domain containing 1 |
PLCXD1 database at LOVD
http://www.LOVD.nl/PLCXD1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PLEC
plectin 601282 |
Leiden Muscular Dystrophy pages - Plectin (PLEC)
http://www.LOVD.nl/PLEC |
Johan T den Dunnen Leiden Univ. Med Centre |
PLOD2
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 601865 |
Osteogenesis Imperfecta Variant Database
http://oi.gene.le.ac.uk/home.php?select_db=PLOD2 |
Raymond Dalgleish |
PLP1
proteolipid protein 1 300401 |
Mental Retardation database proteolipid protein 1 (PLP1)
http://www.LOVD.nl/PLP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PLP2
proteolipid protein 2 (colonic epithelium-enriched) 300112 |
Mental Retardation database proteolipid protein 2 (colonic epithelium-enriched) (PLP2)
http://www.LOVD.nl/PLP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PLS3
plastin 3 300131 |
PLS3 database at LOVD
http://www.LOVD.nl/PLS3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PLXNA3
plexin A3 300022 |
PLXNA3 database at LOVD
http://www.LOVD.nl/PLXNA3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PLXNB3
plexin B3 300214 |
PLXNB3 database at LOVD
http://www.LOVD.nl/PLXNB3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PMM2
phosphomannomutase 2 601785 |
Congenital Disorders of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs, Center for Human Genetics Leuven, Belgium |
PMP22
peripheral myelin protein 22 601097 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
PMS1
PMS1 postmeiotic segregation increased 1 (S. cerevisiae) 600258 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC) |
PMS1
PMS1 postmeiotic segregation increased 1 (S. cerevisiae) 600258 |
Zhejiang University-Adinovo Center PMS1 Database
http://www.china-hvp.org/LOVD/?select_db=PMS1 |
Ming Qi, PhD, FACMG, Peikuan Cong, Shu Zheng, MD, Yudong Gao and Changsong Lin |
PMS2
PMS2 postmeiotic segregation increased 2 (S. cerevisiae) 600259 |
Hereditary Non-Polyposis Colorectal Cancer, HNPCC
http://www.insight-group.org/ |
International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer (ICG-HNPCC) |
PMS2
PMS2 postmeiotic segregation increased 2 (S. cerevisiae) 600259 |
Zhejiang University-Adinovo Center PMS2 Database
http://www.china-hvp.org/LOVD/?select_db=PMS2 |
Ming Qi, PhD, FACMG, Peikuan Cong, Shu Zheng, MD, Yudong Gao and Changsong Lin |
PNMA3
paraneoplastic antigen MA3 300675 |
PNMA3 database at LOVD
http://www.LOVD.nl/PNMA3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PNMA5
paraneoplastic antigen like 5 |
PNMA5 database at LOVD
http://www.LOVD.nl/PNMA5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PNMA6A
paraneoplastic antigen like 6A |
PNMA6A database at LOVD
http://www.LOVD.nl/PNMA6A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PNP
purine nucleoside phosphorylase 164050 |
NPbase: Mutation registry for PNP deficiency
http://bioinf.uta.fi/NPbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
PNPLA4
patatin-like phospholipase domain containing 4 300102 |
PNPLA4 database at LOVD
http://www.LOVD.nl/PNPLA4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PNPO
pyridoxamine 5'-phosphate oxidase 603287 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
POF1B
premature ovarian failure, 1B 300603 |
POF1B database at LOVD
http://www.LOVD.nl/POF1B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
POLA1
polymerase (DNA directed), alpha 1, catalytic subunit 312040 |
POLA1 database at LOVD
http://www.LOVD.nl/POLA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
POMGNT1
protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 606822 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/POMGNT1 |
Ros�rio dos Santos & Johan den Dunnen |
POMT1
protein-O-mannosyltransferase 1 607423 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/POMT1 |
Ros�rio dos Santos & Johan den Dunnen |
POMT2
protein-O-mannosyltransferase 2 607439 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/POMT2 |
Ros�rio dos Santos & Johan den Dunnen |
POR
P450 (cytochrome) oxidoreductase 124015 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
PORCN
porcupine homolog (Drosophila) 300651 |
PORCN at LOVD
http://www.LOVD.nl/PORCN |
M.P. Lombardi and R.C.M. Hennekam, Academic Medical Center, University of Amsterdam |
POU3F4
POU class 3 homeobox 4 300039 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
POU3F4
POU class 3 homeobox 4 300039 |
POU3F4 database at LOVD
http://www.LOVD.nl/POU3F4 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
POU4F3
POU class 4 homeobox 3 602460 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
PPEF1
protein phosphatase, EF-hand calcium binding domain 1 300109 |
PPEF1 database at LOVD
http://www.LOVD.nl/PPEF1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PPIB
peptidylprolyl isomerase B (cyclophilin B) 123841 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
PPP1R3F
protein phosphatase 1, regulatory (inhibitor) subunit 3F |
PPP1R3F database at LOVD
http://www.LOVD.nl/PPP1R3F |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PPP2R3B
protein phosphatase 2 (formerly 2A), regulatory subunit B'', beta 300339 |
PPP2R3B database at LOVD
http://www.LOVD.nl/PPP2R3B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PPT1
palmitoyl-protein thioesterase 1 600722 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole, MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
PPT1
palmitoyl-protein thioesterase 1 600722 |
Mutations of the Palmitoyl-Protein Thioesterase Gene (PPT CLN1) Gene
http://www.retina-international.org/sci-news/pptmut.htm |
Retina International |
PQBP1
polyglutamine binding protein 1 300463 |
PQBP1 database at LOVD
http://www.LOVD.nl/PQBP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRDX4
peroxiredoxin 4 606506 |
PRDX4 database at LOVD
http://www.LOVD.nl/PRDX4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRF1
perforin 1 (pore forming protein) 170280 |
PRF1base: Mutation registry for Familiar haemophagocytic lymphohistiocytosis, type II (FHL2)
http://bioinf.uta.fi/PRF1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
PRF1
perforin 1 (pore forming protein) 170280 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
http://www.LOVD.nl/PRF1 |
Ammar Husami and Theru A. Sivakumaran |
PRICKLE3
prickle homolog 3 (Drosophila) 300111 |
PRICKLE3 database at LOVD
http://www.LOVD.nl/PRICKLE3 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRKCG
protein kinase C, gamma 176980 |
Mutations of the Protein Kinase C γ
http://www.retina-international.org/sci-news/prkcgmut.htm |
Retina International |
PRKX
protein kinase, X-linked 300083 |
PRKX database at LOVD
http://www.LOVD.nl/PRKX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRNP
prion protein 176640 |
Prion Protein/CJD database
http://www.mad-cow.org/~tom/prion_point_mutations.html |
Sperling Biomedical Foundation, Oregon, U.S.A. |
PROM1
prominin 1 604365 |
Mutations of the Prominin (mouse)-like 1 gene (PROML1)
http://www.retina-international.org/sci-news/promlmut.htm |
Retina International |
PROM1
prominin 1 604365 |
Prominin 1 (PROM1) database at LOVD
http://www.LOVD.nl/PROM1 |
Pascal Escher, IRO-Institut de Recherche en Ophtalmologie, Switzerland |
PROS1
protein S (alpha) 176880 |
Protein S Deficiency: A database of Mutations
http://www.med.unc.edu/isth/ |
S. Gandrille, INSERM U. 428, UFR des Sciences Pharmaceutiques et Biologiques, 4 Avenue de l'Observatoire, 75006 Paris, FRANCE |
Protein Kinase
multiple protein kinase domains |
KinMutBase: A registry of disease-causing mutations in protein kinase domains
http://bioinf.uta.fi/KinMutBase/ |
Mauno Vihinen, Kaj Stenberg, Univ. of Tampere, Tampere, Finland |
PRPF31
PRP31 pre-mRNA processing factor 31 homolog (S. cerevisiae) 606419 |
Mutations of the RNA Processing Factor 31
http://www.retina-international.org/sci-news/prp31mut.htm |
Retina International |
PRPF8
PRP8 pre-mRNA processing factor 8 homolog (S. cerevisiae) 607300 |
Mutations of the Precursor mRNA Processing Protein 8
http://www.retina-international.org/sci-news/prpc8mut.htm |
Retina International |
PRPH2
peripherin 2 (retinal degeneration, slow) 179605 |
Mutations of the RDS/Peripherin Gene
http://www.retina-international.org/sci-news/rdsmut.htm |
Retina International |
PRPS1
phosphoribosyl pyrophosphate synthetase 1 311850 |
PRPS1 database at LOVD
http://www.LOVD.nl/PRPS1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRPS2
phosphoribosyl pyrophosphate synthetase 2 311860 |
PRPS2 database at LOVD
http://www.LOVD.nl/PRPS2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRRG1
proline rich Gla (G-carboxyglutamic acid) 1 604428 |
PRRG1 database at LOVD
http://www.LOVD.nl/PRRG1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRRG3
proline rich Gla (G-carboxyglutamic acid) 3 (transmembrane) 300685 |
PRRG3 database at LOVD
http://www.LOVD.nl/PRRG3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PRSS1
protease, serine, 1 (trypsin 1) 276000 |
Database of genetic variants in patients with chronic pancreatitis
http://www.uni-leipzig.de/pancreasmutation/ |
Niels Teich, Universit�t Leipzig, Medizinische Klinik und Poliklinik IID-04103 Leipzig, Germany |
PRX
periaxin 605725 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
PSEN1
presenilin 1 104311 |
Alzheimer Disease & Frontotemporal Dementia Mutation Database
http://www.molgen.ua.ac.be/ADMutations/ |
Marc Cruts & Nathalie Brouwers Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
PSEN2
presenilin 2 (Alzheimer disease 4) 600759 |
Alzheimer Disease & Frontotemporal Dementia Mutation Database
http://www.molgen.ua.ac.be/ADMutations/ |
Marc Cruts & Nathalie Brouwers, Molecular Genetics Department, Flanders Interuniversity, Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
PSMD10
proteasome (prosome, macropain) 26S subunit, non-ATPase, 10 603480 |
PSMD10 database at LOVD
http://www.LOVD.nl/PSMD10 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PSTPIP1
proline-serine-threonine phosphatase interacting protein 1 606347 |
PAPA syndrome: INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Carol Wise, Seay Center for Musculoskeletal Research, Texas Scottish Rite Hospital for Children,Dallas, USA |
PTCH1
patched homolog 1 (Drosophila) 601309 |
PTCH Mutation Database
http://www.cybergene.se/cgi-bin/w3-msql/ptchbase/index.html |
Rune Toftgard, Karolinska Institut, Sweden Georgia Chenevix-Trench, QIMR, Brisbane, Australia Mike Dean, National Cancer Institute, Maryland, U.S.A. |
PTCHD1
patched domain containing 1 |
PTCHD1 database at LOVD
http://www.LOVD.nl/PTCHD1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
PTGIS
prostaglandin I2 (prostacyclin) synthase 601699 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
PTPRC
protein tyrosine phosphatase, receptor type, C 151460 |
PTPRCbase: Mutation registry for CD45 deficiency
http://bioinf.uta.fi/PTPRCbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
PTRF
polymerase I and transcript release factor 603198 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/PTRF |
Johan T. den Dunnen Leiden Univ. Med Centre, other curators invited |
PTS
6-pyruvoyltetrahydropterin synthase 261640 |
6-Pyruvoyl-tetrahydropterinsynthase deficiency-BIOMED database
http://www.bh4.org/ |
N. Blau, Univ.Children's Hospital, Zurich J.L. Dhont, Facult� libre de M�dicine, Lille, France I.Dianzani, Univ.Torino, Torino, Italy |
Go Back To Main Index! | ||
QDPR
quinoid dihydropteridine reductase 261630 |
Quinoid Dihydropteridinereductase deficiency- BIOMED database
http://www.bh4.org/ |
N. Blau, Univ.Children's Hospital, Zurich J.L. Dhont, Facult� libre de M�dicine, Lille, France I.Dianzani, Univ.Torino, Torino, Italy |
Go Back To Main Index! | ||
RAB27A
RAB27A, member RAS oncogene family 603868 |
RAB27Abase: Mutation registry for Griscelli syndrome, type 2 (GS2)
http://bioinf.uta.fi/RAB27Abase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
RAB27A
RAB27A, member RAS oncogene family 603868 |
Mutations of the Small Nucleotide-binding Protein 27a Gene
http://www.retina-international.org/sci-news/rab27mut.htm |
Retina International |
RAB27A
RAB27A, member RAS oncogene family 603868 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/RAB27A |
Ammar Husami and Theru A. Sivakumaran |
RAB33A
RAB33A, member RAS oncogene family 300333 |
RAB33A database at LOVD
http://www.LOVD.nl/RAB33A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAB39B
RAB39B, member RAS oncogene family 300774 |
RAB39B database at LOVD
http://www.LOVD.nl/RAB39B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAB40A
RAB40A, member RAS oncogene family |
RAB40A database at LOVD
http://www.LOVD.nl/RAB40A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAB40AL
RAB40A, member RAS oncogene family-like 300405 |
RAB40AL database at LOVD
http://www.LOVD.nl/RAB40AL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAB41
RAB41, member RAS oncogene family |
RAB41 database at LOVD
http://www.LOVD.nl/RAB41 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAB7A
RAB7A, member RAS oncogene family 602298 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
RAB9B
RAB9B, member RAS oncogene family 300285 |
RAB9B database at LOVD
http://www.LOVD.nl/RAB9B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RAC2
ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) 602049 |
RAC2base: Mutation registry for Neutrophil immunodeficiency syndrome
http://bioinf.uta.fi/RAC2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
RAG1
recombination activating gene 1 179615 |
RAG1base: Mutation registry for autosomal recessive RAG1 deficiency
http://bioinf.uta.fi/RAG1base/ |
Mauno Vihinen, Anna Villa, Univ. of Tampere, Tampere, Finland |
RAG2
recombination activating gene 2 179616 |
RAG2base: Mutation registry for autosomal recessive RAG2 deficiency
http://bioinf.uta.fi/RAG2base/ |
Mauno Vihinen, Anna Villa, Univ. of Tampere, Tampere, Finland |
RAI2
retinoic acid induced 2 300217 |
RAI2 database at LOVD
http://www.LOVD.nl/RAI2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RB1
retinoblastoma 1 180200 |
rb1-lsdb, Universitat Duisburg-Essen
http://www.verandi.de/joomla/index.php?option=com_frontpage&Itemid=1 |
Dietmar R. Lohmann and Julia R�wenstrunk, Universitat Duisburg-Essen, Germany |
RBM10
RNA binding motif protein 10 300080 |
RBM10 database at LOVD
http://www.LOVD.nl/RBM10 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RBM41
RNA binding motif protein 41 |
RBM41 database at LOVD
http://www.LOVD.nl/RBM41 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RBMX
RNA binding motif protein, X-linked 300199 |
RBMX database at LOVD
http://www.LOVD.nl/RBMX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RDH5
retinol dehydrogenase 5 (11-cis/9-cis) 601617 |
Mutations of the 11-cis Retinol Dehydrogenase Gene
http://www.retina-international.org/sci-news/rdhmut.htm |
Retina International |
RENBP
renin binding protein 312420 |
RENBP database at LOVD
http://www.LOVD.nl/RENBP |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
REPS2
RALBP1 associated Eps domain containing 2 300317 |
REPS2 database at LOVD
http://www.LOVD.nl/REPS2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RET
ret proto-oncogene 164761 |
Multiple Endocrine Neoplasia type 2 (MEN2) RET database
http://www.arup.utah.edu/database/MEN2/MEN2_welcome.php |
Dr. Rebecca Margraf and Dr. Rong Mao, ARUP Institute for Clinical and Experimental Pathology(r), Salt Lake City, UT, USA |
RFX5
regulatory factor X, 5 (influences HLA class II expression) 601863 |
RFX5base: Mutation registry for MHCII promoter X box regulatory factor 5 deficiency
http://bioinf.uta.fi/RFX5base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
RFXANK
regulatory factor X-associated ankyrin-containing protein 603200 |
RFXANKbase: Mutation registry for Ankyrin repeat containing regulatory factor X-associated protein deficiency
http://bioinf.uta.fi/RFXANKbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
RFXAP
regulatory factor X-associated protein 601861 |
RFXAPbase: Mutation registry for Regulatory factor X-associated protein deficiency
http://bioinf.uta.fi/RFXAPbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
RGAG1
retrotransposon gag domain containing 1 |
RGAG1 database at LOVD
http://www.LOVD.nl/RGAG1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RGAG4
retrotransposon gag domain containing 4 |
RGAG4 database at LOVD
http://www.LOVD.nl/RGAG4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RGR
retinal G protein coupled receptor 600342 |
Mutations of the RPE-Retinal G-Protein-Coupled Receptor
http://www.retina-international.org/sci-news/rgrmut.htm |
Retina International |
RHAG
Rh-associated glycoprotein 180297 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
RHCE
Rh blood group, CcEe antigens 111700 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
RHD
Rh blood group, D antigen 111680 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
RHO
rhodopsin 180380 |
Mutations of the Rhodopsin Gene
http://www.retina-international.org/sci-news/rhomut.htm |
Retina International |
RIPPLY1
ripply1 homolog (zebrafish) 300575 |
RIPPLY1 database at LOVD
http://www.LOVD.nl/RIPPLY1 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RLIM
ring finger protein, LIM domain interacting 300379 |
RLIM database at LOVD
http://www.LOVD.nl/RLIM |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RNF113A
ring finger protein 113A |
RNF113A database at LOVD
http://www.LOVD.nl/RNF113A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RNF128
ring finger protein 128 300439 |
RNF128 database at LOVD
http://www.LOVD.nl/RNF128 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RNF135
ring finger protein 135 611358 |
RNF135 at LOVD
http://www.LOVD.nl/RNF135 |
Monique Losekoot, LUMC, Leiden, Netherlands |
ROM1
retinal outer segment membrane protein 1 180721 |
Mutations of the Rod Outer Membrane Proteine 1 (ROM1) Gene
http://www.retina-international.org/sci-news/rommut.htm |
Retina International |
ROR2
receptor tyrosine kinase-like orphan receptor 2 602337 |
ROR2 database at LOVD
http://www.LOVD.nl/ROR2 |
Jacopo Celli, LUMC, The Netherlands |
RP1
retinitis pigmentosa 1 (autosomal dominant) 603937 |
Mutations of the RP1 Gene
http://www.retina-international.org/sci-news/rp1mut.htm |
Retina International |
RP2
retinitis pigmentosa 2 (X-linked recessive) 312600 |
Mutations of the RP2 Gene
http://www.retina-international.org/sci-news/rp2mut.htm |
Retina International |
RP2
retinitis pigmentosa 2 (X-linked recessive) 300757 |
RP2 database at LOVD
http://www.LOVD.nl/RP2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPA4
replication protein A4, 30kDa 300767 |
RPA4 database at LOVD
http://www.LOVD.nl/RPA4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPE65
retinal pigment epithelium-specific protein 65kDa 180069 |
Mutations of the RPE65 Gene
http://www.retina-international.org/sci-news/rpe65mut.htm |
Retina International |
RPGR
retinitis pigmentosa GTPase regulator 312610 |
Mutations of the Retinitis Pigmentosa GTPase Regulator (RPGR) Gene
http://www.retina-international.org/sci-news/rpgrmut.htm |
Retina International |
RPGR
retinitis pigmentosa GTPase regulator 312610 |
RPGR @ The Human Genetics Unit Edinburgh U.K.
http://rpgr.hgu.mrc.ac.uk/ |
Xinhua Shu and Alan Wright |
RPGR
retinitis pigmentosa GTPase regulator 312610 |
RPGR database at LOVD
http://www.LOVD.nl/RPGR |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPGRIP1
retinitis pigmentosa GTPase regulator interacting protein 1 605446 |
Mutations of the Retinitis Pigmentosa GTPase Regulator Interacting Protein Gene
http://www.retina-international.org/sci-news/rpgripmu.htm |
Retina International |
RPL10
ribosomal protein L10 312173 |
RPL10 database at LOVD
http://www.LOVD.nl/RPL10 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPL11
ribosomal protein L11 604175 |
Diamond-Blackfan Anemia, ribosomal protein L11 (RPL11)
http://www.dbagenes.unito.it/home.php?select_db=RPL11 |
Illenia Boria and Ugo Ramenghi |
RPL35A
ribosomal protein L35a 180468 |
Diamond-Blackfan Anemia, ribosomal protein L35a (RPL35A)
http://www.dbagenes.unito.it/home.php?select_db=RPL35A |
Illenia Boria and Ugo Ramenghi |
RPL36A
ribosomal protein L36a |
RPL36A database at LOVD
http://www.LOVD.nl/RPL36A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPL39
ribosomal protein L39 601904 |
RPL39 database at LOVD
http://www.LOVD.nl/RPL39 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPL5
ribosomal protein L5 603634 |
Diamond-Blackfan Anemia, ribosomal protein L5 (RPL5)
http://www.dbagenes.unito.it/home.php?select_db=RPL5 |
Illenia Boria and Ugo Ramenghi |
RPL9P7
ribosomal protein L9 pseudogene 7 |
RPL9P7 database at LOVD
http://www.LOVD.nl/RPL9P7 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPS17
ribosomal protein S17 180472 |
Diamond-Blackfan Anemia
ribosomal protein S17 (RPS17)
http://www.dbagenes.unito.it/home.php?select_db=RPS17 |
Illenia Boria and Ugo Ramenghi |
RPS19
ribosomal protein S19 603474 |
Diamond-Blackfan Anemia ribosomal protein S19 (RPS19)
http://www.dbagenes.unito.it/home.php?select_db=RPS19 |
Illenia Boria and Ugo Ramenghi |
RPS24
ribosomal protein S24 602412 |
Diamond-Blackfan Anemia
ribosomal protein S24 (RPS24)
http://www.dbagenes.unito.it/home.php?select_db=RPS24 |
Illenia Boria and Ugo Ramenghi |
RPS26P11
ribosomal protein S26 pseudogene 11 |
RPS26P11 database at LOVD
http://www.LOVD.nl/RPS26P11 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPS4X
ribosomal protein S4, X-linked 312760 |
RPS4X database at LOVD
http://www.LOVD.nl/RPS4X |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPS6KA3
ribosomal protein S6 kinase, 90kDa, polypeptide 3 300075 |
Coffin-Lowry Syndrome
http://alsace.u-strasbg.fr/chimbio/diag/coffin/index.html |
University of Strasbourg, France |
RPS6KA3
ribosomal protein S6 kinase, 90kDa, polypeptide 3 300075 |
RPS6KA3 database at LOVD
http://www.LOVD.nl/RPS6KA3 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPS6KA6
ribosomal protein S6 kinase, 90kDa, polypeptide 6 300303 |
RPS6KA6 database at LOVD
http://www.LOVD.nl/RPS6KA6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
RPS7
ribosomal protein S7 603658 |
Diamond-Blackfan Anemia
ribosomal protein S7 (RPS7)
http://www.dbagenes.unito.it/home.php?select_db=RPS7 |
Illenia Boria and Ugo Ramenghi |
RS1
retinoschisin 1 312700 |
X-Linked Juvenile Retinoschisis
http://www.LOVD.nl/RS1 |
Markus Preising & Johan den Dunnen, Leiden Univ. Medical Centre, Leiden, The Netherlands |
RS1
retinoschisin 1 312700 |
Mutations of the X-linked Retinoschisis Gene
http://www.retina-international.org/sci-news/xlrsmut.htm |
Retina International |
RYR1
ryanodine receptor 1 (skeletal) 180901 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/RYR1 |
Johan T. den Dunnen Leiden Univ. Med Centre |
RYR2
ryanodine receptor 2 (cardiac) 180902 |
Gene Connection for the Heart - Catecholaminergic Polymorphic Ventricular Tachycardia
http://www.fsm.it/cardmoc/ |
C. Napolitano, Luciana deGiuli and Andrea Zuanetti, Pavia, Italy |
Go Back To Main Index! | ||
SACS
spastic ataxia of Charlevoix-Saguenay (sacsin) 604490 |
SACSIN- Related autosomal recessive ataxia
http://www.medgen.mcgill.ca/SACSIN/ |
Bernard Brais, Isabelle Thiffault CHUM Notre-Dame Hospital Montreal, Canada |
SAG
S-antigen; retina and pineal gland (arrestin) 181031 |
Mutations of the Arrestin Gene
http://www.retina-international.org/sci-news/sagmut.htm |
Retina International |
SAGE1
sarcoma antigen 1 300359 |
SAGE1 database at LOVD
http://www.LOVD.nl/SAGE1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SASH3
SAM and SH3 domain containing 3 300441 |
SASH3 database at LOVD
http://www.LOVD.nl/SASH3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SATL1
spermidine/spermine N1-acetyl transferase-like 1 |
SATL1 database at LOVD
http://www.LOVD.nl/SATL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SBDS
Shwachman-Bodian-Diamond syndrome 607444 |
SBDSbase: Mutation registry for Shwachman-Diamond syndrome
http://bioinf.uta.fi/SBDSbase/ |
L�szl� Mar�di and Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SBF2
SET binding factor 2 607697 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SCML2
sex comb on midleg-like 2 (Drosophila) 300208 |
SCML2 database at LOVD
http://www.LOVD.nl/SCML2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SCN4A
sodium channel, voltage-gated, type IV, alpha subunit 603967 |
SCN4A at LOVD
http://www.LOVD.nl/SCN4A |
Ieke Ginjaar & Vincent Janmaat, LUMC, Leiden, The Netherlands |
SCN4B
sodium channel, voltage-gated, type IV, beta 608256 |
Zhejiang University-Adinovo Center SCN4B Database
http://china-hvp.org/LOVD/?select_db=SCN4B |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
SCN5A
sodium channel, voltage-gated, type V, alpha subunit 600163 |
Long QT Syndrome mutation database
http://www.ssi.dk/graphics/html/lqtsdb/lqtsdb.htm |
Michael Christiansen, Lars A. Larsen, Paal Skytt Andersen, Molecular Cardiology grp, Statens Serum Institut, Copenhagen, Denmark |
SCN5A
sodium channel, voltage-gated, type V, alpha subunit 600163 |
Gene Connection for the Heart
http://www.fsm.it/cardmoc/ |
P. Brugada, Alalst, Belgium; J. Brugada, Banyoles, Spain; R. Brugada, Houston, Texas, U.S.A.; A.A.M. Wilde Amsterdam, The Netherlands |
SCN5A
sodium channel, voltage-gated, type V, alpha subunit 600163 |
Zhejiang University-Adinovo Center SCN5A Database
http://china-hvp.org/LOVD/?select_db=SCN5A |
Ming Qi, PhD, FACMG, Peikuan Cong and Yudong Gao |
SCNN1A
sodium channel, nonvoltage-gated 1 alpha 600228 |
SCNN1A Database at LOVD
http://www.LOVD.nl/SCNN1A |
Azad AK Ontario Cancer Institute, Toronto, Canada |
SCNN1B
sodium channel, nonvoltage-gated 1, beta 600760 |
SCNN1B Database at LOVD
http://www.LOVD.nl/SCNN1B |
Azad AK Ontario Cancer Institute, Toronto, Canada |
SCNN1G
sodium channel, nonvoltage-gated 1, gamma 600761 |
SCNN1G Database at LOVD
http://www.LOVD.nl/SCNN1G |
Azad AK Ontario Cancer Institute, Toronto, Canada |
SDHA
succinate dehydrogenase complex, subunit A, flavoprotein (Fp) 600857 |
SDHA at LOVD
http://www.LOVD.nl/SDHA |
J.P.L. Bayley, Peter E.M. Taschner, Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands |
SDHB
succinate dehydrogenase complex, subunit B, iron sulfur (Ip) 185470 |
SDHB at LOVD
http://www.LOVD.nl/SDHB |
J.P.L. Bayley, Peter E.M. Taschner, Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands |
SDHC
succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa 602413 |
SDHC at LOVD
http://www.LOVD.nl/SDHC |
J.P.L. Bayley, Peter E.M. Taschner, Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands |
SDHD
succinate dehydrogenase complex, subunit D, integral membrane protein 602690 |
SDHD at LOVD
http://www.LOVD.nl/SDHD |
J.P.L. Bayley, Peter E.M. Taschner, Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands |
SEPN1
selenoprotein N, 1 606210 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SEPN1 |
Johan den Dunnen, Tom Winder |
SEPT6
septin 6 300683 |
SEPT6 database at LOVD
http://www.LOVD.nl/SEPT6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SEPT9
septin 9 604061 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity Institute for Biotechnology (VIB,) University of Antwerp (UA), Belgium |
SERPINA1
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1 107400 |
A1ATVar: A1-antitrypsin database
http://www.goldenhelix.org/a1atvar/ |
G.P. Patrinos and S. Zaimidou |
SERPINA1
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1 107400 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/SERPINA1 |
Ammar Husami and Theru A. Sivakumaran |
SERPINA7
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7 314200 |
SERPINA7 database at LOVD
http://www.LOVD.nl/SERPINA7 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SERPINC1
serpin peptidase inhibitor, clade C (antithrombin), member 1 107300 |
Antithrombin III mutation database
http://www1.imperial.ac.uk/medicine/about/divisions/departmentofmedicine/experimentalmedicine/haematology/coag/antithrombin/ |
David A. Lane, Imperial college, Sch. of Med., London, U.K. |
SERPINF1
serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1 172860 |
Osteogenesis Imperfecta Variation Database
http://www.le.ac.uk/genetics/collagen |
Raymond Dalgleish |
SERPING1
serpin peptidase inhibitor, clade G (C1 inhibitor), member 1 606860 |
SERPING1base: Mutation registry for Hereditary angioedema
http://bioinf.uta.fi/SERPING1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SERPINH1
serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) 600943 |
Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants
http://www.le.ac.uk/genetics/collagen/ |
Raymond Dalgleish, Leicester, U.K. |
SETX
senataxin 608465 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SETX
senataxin 608465 |
UCLA Neurogenetics SETX Database
http://149.142.212.78/LOVD/ |
Abhishek Goel, Giovanni Coppola, and Brent Fogel |
SFRS17A
splicing factor, arginine/serine-rich 17A 465000 |
SFRS17A database at LOVD
http://www.LOVD.nl/SFRS17A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SGCA
sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) 600119 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCA |
Johan T. den Dunnen, Leiden Univ.Med Centre, Leiden, The Netherlands |
SGCB
sarcoglycan, beta (43kDa dystrophin-associated glycoprotein) 600900 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCB |
Johan T. den Dunnen, Leiden Univ.Med Centre, Leiden, The Netherlands |
SGCD
sarcoglycan, delta (35kDa dystrophin-associated glycoprotein) 601411 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCD |
Johan T. den Dunnen, Leiden Univ.Med Centre, Leiden, The Netherlands |
SGCE
sarcoglycan, epsilon 604149 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCE |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands |
SGCG
sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) 608896 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCG |
Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands |
SGCZ
sarcoglycan, zeta 608113 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/SGCZ |
Johan den Dunnen, LUMC, Leiden, Netherlands |
SH2D1A
SH2 domain containing 1A 300490 |
SH2D1Abase: Mutation registry for X-linked lymphoproliferative syndrome (XLP)
http://bioinf.uta.fi/SH2D1Abase/ |
Luigi D. Notarangelo, Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SH2D1A
SH2 domain containing 1A 300490 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/SH2D1A |
Ammar Husami and Theru A. Sivakumaran |
SH3KBP1
SH3-domain kinase binding protein 1 300374 |
SH3KBP1 database at LOVD
http://www.LOVD.nl/SH3KBP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SH3TC2
SH3 domain and tetratricopeptide repeats 2 608206 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SHOX
short stature homeobox 312865 |
SHOX database at Heidelberg University
http://hyg-serv-01.hyg.uni-heidelberg.de/lovd/index.php?select_db=SHOX |
Steffi Wilke, Dr. Beate Niesler, Ralph Roeth and Prof. Gudrun Rappold |
SHROOM2
shroom family member 2 300103 |
SHROOM2 database at LOVD
http://www.LOVD.nl/SHROOM2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SHROOM4
shroom family member 4 300579 |
SHROOM4 database at LOVD
http://www.LOVD.nl/SHROOM4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SIAH1L
seven in absentia homolog 1-like (Drosophila) |
SIAH1L database at LOVD
http://www.LOVD.nl/SIAH1L |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC10A3
solute carrier family 10 (sodium/bile acid cotransporter family), member 3 312090 |
SLC10A3 database at LOVD
http://www.LOVD.nl/SLC10A3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC12A6
solute carrier family 12 (potassium/chloride transporters), member 6 604878 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SLC14A1
solute carrier family 14 (urea transporter), member 1 (Kidd blood group) 111000 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
SLC16A2
solute carrier family 16, member 2 (monocarboxylic acid transporter 8) 300095 |
SLC16A2 database at LOVD
http://www.LOVD.nl/SLC16A2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC22A5
solute carrier family 22 (organic cation/carnitine transporter), member 5 603377 |
Primary Carnitine Deficiency (OCTN2) and SLC22A5 gene Database
http://www.arup.utah.edu/database/OCTN2/OCTN2_welcome.php |
Fernanda Calderon, MS, ARUP Institute for Clinical and Experimental Pathology(r), Salt Lake City, UT, USA |
SLC25A13
solute carrier family 25, member 13 (citrin) 603859 |
SLC25A13
http://www.LOVD.nl/SLC25A13 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC25A14
solute carrier family 25 (mitochondrial carrier, brain), member 14 300242 |
SLC25A14 database at LOVD
http://www.LOVD.nl/SLC25A14 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC25A15
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 603861 |
SLC25A15 database at LOVD
http://www.LOVD.nl/SLC25A15 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC25A43
solute carrier family 25, member 43 300641 |
SLC25A43 database at LOVD
http://www.LOVD.nl/SLC25A43 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC25A5
solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5 300150 |
SLC25A5 database at LOVD
http://www.LOVD.nl/SLC25A5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC25A6
solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6 403000 |
SLC25A6 database at LOVD
http://www.LOVD.nl/SLC25A6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC26A4
solute carrier family 26, member 4 605646 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
SLC26A4
solute carrier family 26, member 4 605646 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=SLC26A4 |
Ammar Husami and Theru A. Sivakumaran |
SLC29A3
solute carrier family 29 (nucleoside transporters), member 3 612373 |
SLC29A3 database at LOVD
http://www.LOVD.nl/SLC29A3 |
Dr Neil Morgan and Dr. Derek Lim |
SLC35C1
solute carrier family 35, member C1 605881 |
Congenital Disorder of Glycosylation pages
http://www.euroglycanet.org/ |
Gert Matthijs Center for Human Genetics Leuven, Belgium |
SLC35C1
solute carrier family 35, member C1 605881 |
SLC35C1base: Mutation registry for Leucocyte adhesion deficiency I I (LAD-II) (previously known as FUCT1base)
http://bioinf.uta.fi/SLC35C1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SLC38A5
solute carrier family 38, member 5 300649 |
SLC38A5 database at LOVD
http://www.LOVD.nl/SLC38A5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC45A2
solute carrier family 45, member 2 606202 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota, U.S.A. |
SLC45A2
solute carrier family 45, member 2 606202 |
Mutations of the Membrane-associated Transport Protein Gene (MATP)
http://www.retina-international.org/sci-news/matpmut.htm |
Retina International |
SLC4A1
solute carrier family 4, anion exchanger, member 1 (erythrocyte membrane protein band 3, Diego blood group) 109270 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
SLC6A14
solute carrier family 6 (amino acid transporter), member 14 300444 |
SLC6A14 database at LOVD
http://www.LOVD.nl/SLC6A14 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC6A3
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 126455 |
SLC6A3 database at LOVD
http://www.LOVD.nl/SLC6A3 |
Dr Manju Kurian and Dr. Derek Lim |
SLC6A5
solute carrier family 6 (neurotransmitter transporter, glycine), member 5 604159 |
SLC6A5 database at LOVD
http://www.LOVD.nl/SLC6A5 |
Vincent Janmaat |
SLC6A8
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 300036 |
Creatine transporter: solute carrier family 6 (neurotransmitter transporter (SLC6A8) Variation Database
http://www.LOVD.nl/SLC6A8 |
Gajja Salomons |
SLC7A3
solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 300443 |
SLC7A3 database at LOVD
http://www.LOVD.nl/SLC7A3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC9A6
solute carrier family 9 (sodium/hydrogen exchanger), member 6 300231 |
SLC9A6 database at LOVD
http://www.LOVD.nl/SLC9A6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLC9A7
solute carrier family 9 (sodium/hydrogen exchanger), member 7 300368 |
SLC9A7 database at LOVD
http://www.LOVD.nl/SLC9A7 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLITRK2
SLIT and NTRK-like family, member 2 300561 |
SLITRK2 database at LOVD
http://www.LOVD.nl/SLITRK2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SLITRK4
SLIT and NTRK-like family, member 4 300562 |
SLITRK4 database at LOVD
http://www.LOVD.nl/SLITRK4 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SMAD3
SMAD family member 3 603109 |
SMAD family member 3 (SMAD3) database
http://lovd.bx.psu.edu/home.php?select_db=SMAD3 |
Belinda Giardine and Joseph Borg |
SMAD6
SMAD family member 6 602931 |
SMAD family member 6 (SMAD6) database
http://lovd.bx.psu.edu/home.php?select_db=SMAD6 |
Belinda Giardine and Joseph Borg |
SMARCA1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1 300012 |
SMARCA1 database at LOVD
http://www.LOVD.nl/SMARCA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SMARCAL1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 606622 |
SMARCAL1base: Mutation registry for Schimke immuno-osseous dysplasia
http://bioinf.uta.fi/SMARCAL1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SMC1A
structural maintenance of chromosomes 1A 300040 |
SMC1A database at LOVD
http://www.LOVD.nl/SMC1A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SMC3
structural maintenance of chromosomes 3 606062 |
Cornelia de Lange syndrome, type 3 (CDLS3)
http://www.LOVD.nl/SMC3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SMN1
survival of motor neuron 1, telomeric 600354 |
SMN1 - Spinal Muscular Atrophy (SMA)
http://www.LOVD.nl/SMN1 |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
SMS
spermine synthase 300105 |
SMS database at LOVD
http://www.LOVD.nl/SMS |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SNCA
synuclein, alpha (non A4 component of amyloid precursor) 163890 |
Alpha - Synuclein Locus Mutation Database
http://www.med.upatras.gr/athanassiadou/snca_lsdb.pdf |
Aglaia Athanassiadou, Spyridon Papapetropoulos, Gerassimos Karousos, Univ. of Patras,Greece Mihael Polymeropoulos, Novartis Pharmaceuticals, Gaithersburg,USA |
SNCA
synuclein, alpha (non A4 component of amyloid precursor) 163890 |
SNCA Parkinson's disease Mutation Database
http://www.LOVD.nl/SNCA |
The Parkinson's Institute |
SNTA1
syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) 601017 |
Zhejiang University-Adinovo Center SNTA1 Database
http://www.china-hvp.org/LOVD/?select_db=SNTA1 |
Ming Qi, PhD, FACMG, Peikuan Cong, Yudong Gao and Tao Zhang |
SOD1
superoxide dismutase 1, soluble 147450 |
alsod.orgAn online database for ALS/SOD1 genetic mutations
http://alsod.iop.kcl.ac.uk/Als/Overview/gene.aspx?gene_id=SOD1 |
ALS/SOD1 consortium |
SOST
sclerosteosis 605740 |
LOVD - Leiden Open Variation Database
http://www.LOVD.nl/SOST |
Wim van Hul |
SOX10
SRY (sex determining region Y)-box 10 602229 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SOX10
SRY (sex determining region Y)-box 10 602229 |
SOX10 database at LOVD
http://www.LOVD.nl/SOX10 |
Veronique Pingault Laboratoire de Biochimie et G�n�tique, Hopital Henri Mondor Creteil cedex, France |
SOX2
SRY (sex determining region Y)-box 2 184429 |
SOX2 database at MRC Human Genetics Unit
http://lsdb.hgu.mrc.ac.uk/home.php?select_db=SOX2 |
Graeme Grimes, Isabel Hanson, David FitzPatrick, Kathy Williamson and Veronica van Heyningen |
SOX3
SRY (sex determining region Y)-box 3 313430 |
SOX3 database at LOVD
http://www.LOVD.nl/SOX3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SP110
SP110 nuclear body protein 604457 |
SP110base: Mutation registry for Hepatic veno-occlusive disease with immunodeficiency syndrome (VODI)
http://bioinf.uta.fi/SP110base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SP7
Sp7 transcription factor 606633 |
Osteogenesis Imperfecta Variant Database
http://oi.gene.le.ac.uk/home.php?select_db=SP7 |
Raymond Dalgleish |
SPANXN1
SPANX family, member N1 300664 |
SPANXN1 database at LOVD
http://www.LOVD.nl/SPANXN1 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SPANXN4
SPANX family, member N4 300667 |
SPANXN4 database at LOVD
http://www.LOVD.nl/SPANXN4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SPIN2A
spindlin family, member 2A 300621 |
SPIN2A database at LOVD
http://www.LOVD.nl/SPIN2A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SPINK1
serine peptidase inhibitor, Kazal type 1 167790 |
Database of genetic variants in patients with chronic pancreatitis
http://www.uni-leipzig.de/pancreasmutation/ |
Niels Teich, Universit�t Leipzig, Medizinische Klinik und Poliklinik IID-04103 Leipzig, Germany |
SPINK5
serine peptidase inhibitor, Kazal type 5 605010 |
SPINK5base: Mutation registry for Netherton syndrome
http://bioinf.uta.fi/SPINK5base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
SPR
sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase) 182125 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
SPTLC1
serine palmitoyltransferase, long chain base subunit 1 605712 |
Inherited Peripheral Neuropathies Mutation Database
http://www.molgen.ua.ac.be/CMTMutations/ |
Eva Nelis Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium |
SRPK3
SFRS protein kinase 3 |
SRPK3 database at LOVD
http://www.LOVD.nl/SRPK3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SRPX
sushi-repeat-containing protein, X-linked 300187 |
SRPX database at LOVD
http://www.LOVD.nl/SRPX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SRPX2
sushi-repeat-containing protein, X-linked 2 300642 |
SRPX2 database at LOVD
http://www.LOVD.nl/SRPX2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SSPN
sarcospan (Kras oncogene-associated gene) 601599 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/SSPN |
Johan den Dunnen |
SSX1
synovial sarcoma, X breakpoint 1 312820 |
SSX1 database at LOVD
http://www.LOVD.nl/SSX1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SSX3
synovial sarcoma, X breakpoint 3 300325 |
SSX3 database at LOVD
http://www.LOVD.nl/SSX3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SSX5
synovial sarcoma, X breakpoint 5 300327 |
SSX5 database at LOVD
http://www.LOVD.nl/SSX5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SSX6
synovial sarcoma, X breakpoint 6 (pseudogene) 300541 |
SSX6 database at LOVD
http://www.LOVD.nl/SSX6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
STARD8
StAR-related lipid transfer (START) domain containing 8 300689 |
STARD8 database at LOVD
http://www.LOVD.nl/STARD8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
STAT1
signal transducer and activator of transcription 1, 91kDa 600555 |
STAT1base: Mutation registry for STAT1 deficiency
http://bioinf.uta.fi/STAT1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
STAT5B
signal transducer and activator of transcription 5B 604260 |
STAT5Bbase: Mutation registry for Growth hormone insensitivity with immunodeficiency
http://bioinf.uta.fi/STAT5Bbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
STAT5B
signal transducer and activator of transcription 5B 604260 |
LOVD growth
http://www.LOVD.nl/STAT5B |
R Rosenfeld and V Hwa |
STX11
syntaxin 11 605014 |
STX11base: Mutation registry for Familial haemophagocytic lymphohistiocytosis 4 (FHL4)
http://bioinf.uta.fi/STX11base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
STX11
syntaxin 11 605014 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
http://www.LOVD.nl/STX11 |
Ammar Husami and Theru A. Sivakumaran |
STXBP2
syntaxin binding protein 2 601717 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/STXBP2 |
Ammar Husami and Theru A. Sivakumaran |
SUV39H1
suppressor of variegation 3-9 homolog 1 (Drosophila) 300254 |
SUV39H1 database at LOVD
http://www.LOVD.nl/SUV39H1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SYAP1
synapse associated protein 1, SAP47 homolog (Drosophila) |
SYAP1 database at LOVD
http://www.LOVD.nl/SYAP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SYN1
synapsin I 313440 |
SYN1 database at LOVD
http://www.LOVD.nl/SYN1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SYNE1
spectrin repeat containing, nuclear envelope 1 608441 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/SYNE1 |
Johan T. den Dunnen Leiden Univ. Med Centre |
SYNE2
spectrin repeat containing, nuclear envelope 2 608442 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/SYNE2 |
Johan T. den Dunnen Leiden Univ. Med Centre |
SYP
synaptophysin 313475 |
SYP database at LOVD
http://www.LOVD.nl/SYP |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SYTL4
synaptotagmin-like 4 300723 |
SYTL4 database at LOVD
http://www.LOVD.nl/SYTL4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
SYTL5
synaptotagmin-like 5 |
SYTL5 database at LOVD
http://www.LOVD.nl/SYTL5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
TAB3
TGF-beta activated kinase 1/MAP3K7 binding protein 3 300480 |
TAB3 database at LOVD
http://www.LOVD.nl/TAB3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TAF1
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa 313650 |
TAF1 database at LOVD
http://www.LOVD.nl/TAF1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TAF7L
TAF7-like RNA polymerase II, TATA box binding protein (TBP)-associated factor, 50kDa 300314 |
TAF7L database at LOVD
http://www.LOVD.nl/TAF7L |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TAF9B
TAF9B RNA polymerase II, TATA box binding protein (TBP)-associated factor, 31kDa 300754 |
TAF9B database at LOVD
http://www.LOVD.nl/TAF9B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TAP1
transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 170260 |
TAP1base: Mutation registry for TAP1 deficiency
http://bioinf.uta.fi/TAP1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TAP1
transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 170260 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
TAP2
transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) 170261 |
TAP2base: Mutation registry for TAP2 deficiency
http://bioinf.uta.fi/TAP2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TAP2
transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) 170261 |
IMGT/HLA Database
http://www.ebi.ac.uk/imgt/hla/ |
SGE Marsh, Anthony Nolan Research Institute, Royal Free Hospital, London, UK |
TAPBP
TAP binding protein (tapasin) 601962 |
TAPBPbase: Mutation registry for Tapasin deficiency
http://bioinf.uta.fi/TAPBPbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TAZ
tafazzin 300394 |
TAZbase: Mutation registry for Barth syndrome
http://bioinf.uta.fi/TAZbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TAZ
tafazzin 300394 |
Human Tafazzin (TAZ) Gene Mutation & Variation Database
http://www.barthsyndrome.org/ |
Iris L. Gonzalez, Ph.D., U.S.A. |
TBC1D8B
TBC1 domain family, member 8B (with GRAM domain) |
TBC1D8B database at LOVD
http://www.LOVD.nl/TBC1D8B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TBX22
T-box 22 300307 |
TBX22 database at LOVD
http://www.LOVD.nl/TBX22 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TBXAS1
thromboxane A synthase 1 (platelet) 274180 |
Human Cytochrome P450 (CYP) Allele Nomenclature Committee
http://www.cypalleles.ki.se/ |
Magnus Ingelman-Sundberg, Ann K. Daly, Daniel W. Nebert, Sarah Sim, Karolinska Institutet, Stockholm, Sweden |
TCAP
titin-cap (telethonin) 604488 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TCAP |
Johan T. den Dunnen, Leiden Univ. Medical Centre, Leiden, The Netherlands |
TCEAL2
transcription elongation factor A (SII)-like 2 |
TCEAL2 database at LOVD
http://www.LOVD.nl/TCEAL2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TCEAL4
transcription elongation factor A (SII)-like 4 |
TCEAL4 database at LOVD
http://www.LOVD.nl/TCEAL4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TCEAL5
transcription elongation factor A (SII)-like 5 |
TCEAL5 database at LOVD
http://www.LOVD.nl/TCEAL5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TCEAL8
transcription elongation factor A (SII)-like 8 |
TCEAL8 database at LOVD
http://www.LOVD.nl/TCEAL8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TCF4
transcription factor 4 602272 |
TCF4 database at LOVD
http://www.LOVD.nl/TCF4 |
Johan T. den Dunnen, Leiden Univ. Medical Centre, Leiden, The Netherlands & TCF4 Curator |
TCIRG1
T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3 604592 |
TCIRG1base: Mutation registry for autosomal recessive osteopetrosis
http://bioinf.uta.fi/TCIRG1base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TCN2
transcobalamin II; macrocytic anemia 275350 |
TCN2base: Mutation registry for Transcobalamin II deficiency
http://bioinf.uta.fi/TCN2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TCOF1
Treacher Collins-Franceschetti syndrome 1 606847 |
TCOF1 mutation database
http://genoma.ib.usp.br/TCOF1_database/index.php |
A. Splendore, Dept. of Genetics, B203 Beckman Center, Stanford University |
TECTA
tectorin alpha 602574 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
TERC
telomerase RNA component 602322 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#tr |
Julian J-L Chen at Arizona State University |
TERT
telomerase reverse transcriptase 187270 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#tert |
Julian J-L Chen at Arizona State University |
TEX11
testis expressed 11 300311 |
TEX11 database at LOVD
http://www.LOVD.nl/TEX11 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TEX13A
testis expressed 13A 300312 |
TEX13A database at LOVD
http://www.LOVD.nl/TEX13A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TEX13B
testis expressed 13B 300313 |
TEX13B database at LOVD
http://www.LOVD.nl/TEX13B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TFDP3
transcription factor Dp family, member 3 300772 |
TFDP3 database at LOVD
http://www.LOVD.nl/TFDP3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TFE3
transcription factor binding to IGHM enhancer 3 314310 |
TFE3 database at LOVD
http://www.LOVD.nl/TFE3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TGFB3
transforming growth factor, beta 3 190230 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
TGFB3
transforming growth factor, beta 3 190230 |
ARVD/C Genetic Variants Database
http://grenada.lumc.nl/LOVD2/ARVC/home.php?select_db=TGFB3 |
Paul van der Zwaag |
TGFBR2
transforming growth factor, beta receptor II (70/80kDa) 190182 |
The UMD TGFBR2 mutations database
http://194.167.35.228:2105/ |
G. Collod-B�roud |
TH
tyrosine hydroxylase 191290 |
BIOMDB Database of Mutations Causing Tetrahydrobiopterin Deficiencies and PND
http://www.bh4.org/ |
Nenad Blau, Beat Thony, Gajja Salomons, Support by Swiss National Science Foundation |
THOC2
THO complex 2 300395 |
THOC2 database at LOVD
http://www.LOVD.nl/THOC2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TIMM17B
translocase of inner mitochondrial membrane 17 homolog B (yeast) 300249 |
TIMM17B database at LOVD
http://www.LOVD.nl/TIMM17B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TIMP1
TIMP metallopeptidase inhibitor 1 305370 |
TIMP1 database at LOVD
http://www.LOVD.nl/TIMP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TIMP3
TIMP metallopeptidase inhibitor 3 188826 |
Mutations of the Tissue Inhibitor of Metalloproteases 3 Gene
http://www.retina-international.org/sci-news/timpmut.htm |
Retina International |
TINF2
TERF1 (TRF1)-interacting nuclear factor 2 604319 |
The Telomerase Database
http://telomerase.asu.edu/diseases.html#tinf2 |
Julian J-L Chen at Arizona State University |
TLR7
toll-like receptor 7 300365 |
TLR7 database at LOVD
http://www.LOVD.nl/TLR7 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TLR8
toll-like receptor 8 300366 |
TLR8 database at LOVD
http://www.LOVD.nl/TLR8 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TMC1
transmembrane channel-like 1 606706 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
TMC1
transmembrane channel-like 1 606706 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/TMC1 |
Ammar Husami and Theru A. Sivakumaran |
TMC6
transmembrane channel-like 6 605828 |
TMC6base: Mutation registry for Epidermodysplasia verruciformis (previously known as EVER1base)
http://bioinf.uta.fi/TMC6base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TMC8
transmembrane channel-like 8 605829 |
TMC8base: Mutation registry for Epidermodysplasia verruciformis (previously known as EVER2base)
http://bioinf.uta.fi/TMC8base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TMEM114
transmembrane protein 114 611579 |
TMEM114 database at LOVD
http://www.LOVD.nl/TMEM114 |
Johan T den Dunnen Leiden Univ. Med Centre |
TMEM187
transmembrane protein 187 300059 |
TMEM187 database at LOVD
http://www.LOVD.nl/TMEM187 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TMEM27
transmembrane protein 27 300631 |
TMEM27 database at LOVD
http://www.LOVD.nl/TMEM27 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TMEM43
transmembrane protein 43 612048 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
TMEM43
transmembrane protein 43 612048 |
ARVD/C Genetic Variants Database
http://grenada.lumc.nl/LOVD2/ARVC/home.php?select_db=TMEM43 |
Paul van der Zwaag |
TMIE
transmembrane inner ear 607237 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/TMIE |
Ammar Husami |
TMLHE
trimethyllysine hydroxylase, epsilon 300777 |
TMLHE database at LOVD
http://www.LOVD.nl/TMLHE |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TMPRSS3
transmembrane protease, serine 3 605511 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
TMPRSS3
transmembrane protease, serine 3 605511 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/TMPRSS3 |
Ammar Husami and Theru A. Sivakumaran |
TNFRSF13B
tumor necrosis factor receptor superfamily, member 13B 604907 |
TNFRSF13Bbase: Mutation registry for TACI deficiency
http://bioinf.uta.fi/TNFRSF13Bbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TNFRSF1A
tumor necrosis factor receptor superfamily, member 1A 191190 |
INFEVERS: The repertory of Familial Mediterranean Fever (FMF) and Hereditary Inflammatory Disorders Mutations
http://fmf.igh.cnrs.fr/infevers/ |
Ivona Aksentijevich, ARB, NIAMS/NIH, Bethesda, USA |
TNMD
tenomodulin 300459 |
TNMD database at LOVD
http://www.LOVD.nl/TNMD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TNNI2
troponin I type 2 (skeletal, fast) 191043 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TNNI2 |
Tom Winder & Johan den Dunnen |
TNNI3
troponin I type 3 (cardiac) 191044 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Mol & Clin Genet.Royal Prince Alfred Hosp.Sydney, Australia |
TNNI3
troponin I type 3 (cardiac) 191044 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/TNNI3_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
TNNT1
troponin T type 1 (skeletal, slow) 191041 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/TNNT1 |
Johan T. den Dunnen Leiden Univ. Med Centre |
TNNT2
troponin T type 2 (cardiac) 191045 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Mol & Clin Genet.Royal Prince Alfred Hosp.Sydney, Australia |
TNNT2
troponin T type 2 (cardiac) 191045 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/TNNT2_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
TNNT3
troponin T type 3 (skeletal, fast) 600692 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/TNNT3 |
Johan T. den Dunnen Leiden Univ. Med Centre |
TOX
thymocyte selection-associated high mobility group box 606863 |
Thymocyte selection-associated high mobility group box (TOX) database
http://lovd.bx.psu.edu/home.php?select_db=TOX |
Belinda Giardine and Joseph Borg |
TP53
tumor protein p53 191170 |
IARC TP53 Mutation Database: Human somatic and germline TP53 mutations compiled from the literature
http://www-p53.iarc.fr/ |
M. Olivier, R. Eeles, M. Hollstein, C. C. Harris, P. Hainaut, IARC, Lyon, France |
TP53
tumor protein p53 191170 |
p53 Mutation in Human Cancer
http://p53.free.fr/ |
T. Soussi; C. Beroud, INSERM,Hopital Necker, Enfants Malades, Paris, France |
TP53
tumor protein p53 191170 |
Database of Germline p53 Mutations
http://www.lf2.cuni.cz/projects/germline_mut_p53.htm |
Zdenek Sedlacek & Marie Trkova, Charles Univ. Prague, Czech Republic |
TP53
tumor protein p53 191170 |
p53 Mutation Database Analysis & Search
http://p53.genome.ad.jp/ |
Human Genome Centre Tokyo, Japan |
TP53
tumor protein p53 191170 |
The UMD TP53 mutation database
http://www.umd.be:2072/ |
Thierry Soussi, France |
TP63
tumor protein p63 603273 |
ARVD/C Genes Variants Database
http://www.arvcdatabase.info |
Paul van der Zwaag, Jan Jongbloed and Peter van Tintelen, Dept. of Genetics, Univ Med Center, Groningen, The Netherlands |
TP63
tumor protein p63 603273 |
ARVD/C Genetic Variants Database
http://grenada.lumc.nl/LOVD2/ARVC/home.php?select_db=TP63 |
Paul van der Zwaag |
TPM1
tropomyosin 1 (alpha) 191010 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Mol & Clin Genet.Royal Prince Alfred Hosp.Sydney, Australia |
TPM1
tropomyosin 1 (alpha) 191010 |
Sarcomere Protein Gene Mutation Database
http://genepath.med.harvard.edu/~seidman/cg3/genes/TPM1_info.html |
NHLBI Program for Genomic Applications, Harvard Medical School, Boston, USA |
TPM2
tropomyosin 2 (beta) 190990 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TPM2 |
Tom Winder & Johan den Dunnen |
TPM3
tropomyosin 3 191030 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TPM3 |
Johan den Dunnen and Tom Winder |
TPP1
tripeptidyl peptidase I 607998 |
Neuronal Ceroid Lipofuscinoses; NCL Mutations
http://www.ucl.ac.uk/ncl/ |
Sara E. Mole MRC Laboratory for Molecular Cell Biology, University College London, London, United Kingdom |
TRA@
T cell receptor alpha locus 186880 |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRAJ
T cell receptor alpha joining region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRAV
T cell receptor alpha variable region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRB@
T cell receptor beta locus 186930 |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRBD
T cell receptor beta diversity region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRBJ
T cell receptor beta joining region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRBV
T cell receptor beta variable region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRD@
T cell receptor delta locus 186810 |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRDD
T cell receptor delta diversity region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRDJ
T cell receptor delta locus 186810 |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TRDV
T cell receptor delta variable region |
IMGT, the international ImMunoGeneTics information system�
http://imgt.cines.fr |
Marie-Paule Lefranc, CNRS, Universit� Montpellier II, Montpellier, France |
TREX1
three prime repair exonuclease 1 606609 |
TREX1 database at LOVD
http://www.LOVD.nl/TREX1 |
Boukje de Vries, LUMC, Leiden, Nederland |
TRIM32
tripartite motif-containing 32 602290 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TRIM32 |
Johan T. den Dunnen Leiden Univ. Medical Centre Leiden, The Netherlands |
TRMT2B
TRM2 tRNA methyltransferase 2 homolog B (S. cerevisiae) |
TRMT2B database at LOVD
http://www.LOVD.nl/TRMT2B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TRO
trophinin 300132 |
TRO database at LOVD
http://www.LOVD.nl/TRO |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TRPC5
transient receptor potential cation channel, subfamily C, member 5 300334 |
TRPC5 database at LOVD
http://www.LOVD.nl/TRPC5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TSC1
tuberous sclerosis 1 605284 |
TSC Mutation Database
http://www.LOVD.nl/TSC1 |
Sue Povey & Rosemary Ekong, Galton Laboratory, Biology, University |
TSC2
tuberous sclerosis 2 191092 |
TSC2 Mutation Database
http://www.LOVD.nl/TSC2 |
Sue Povey & Rosemary Ekong, Galton Laboratory, Biology, University |
TSHR
thyroid stimulating hormone receptor 603372 |
TSH Receptor mutation database
http://innere.uniklinikum-leipzig.de/tsh/ |
Ralf Paschke, Department of Internal Medicine III, University of Leipzig, Germany |
TSPAN6
tetraspanin 6 300191 |
TSPAN6 database at LOVD
http://www.LOVD.nl/TSPAN6 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TSPYL2
TSPY-like 2 300564 |
TSPYL2 database at LOVD
http://www.LOVD.nl/TSPYL2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TTN
titin 188840 |
FHC Mutation Database
http://www.angis.org.au/Databases/Heart/heartbreak.html |
Bing Yu, Ronald J. Trent, Dept. Mol & Clin Genet., Royal Prince Alfred Hosp. Sydney, Australia |
TTN
titin 188840 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/TTN |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
TTR
transthyretin 176300 |
Database on Transthyretin Mutations
http://www.ibmc.up.pt/mjsaraiva/ttrmut.html |
Maria Jo�o Mascarenhas Saraiva Amyloid Unit Institute of Molecular & Cellular Biology Porto, Portugal |
TULP1
tubby like protein 1 602280 |
Mutations of the Tubby-like Protein 1 Gene
http://www.retina-international.org/sci-news/tulpmut.htm |
Retina International |
TXLNG
taxilin gamma 300677 |
CXorf15 database at LOVD
http://www.LOVD.nl/CXorf15 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
TYK2
tyrosine kinase 2 176941 |
TYK2base: Mutation registry for TYK2 deficiency
http://bioinf.uta.fi/TYK2base/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
TYR
tyrosinase (oculocutaneous albinism IA) 606933 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting Int. Albinism Centre Univ. of Minnesota, USA |
TYR
tyrosinase (oculocutaneous albinism IA) 606933 |
Mutations of the Tyrosinase Gene
http://www.retina-international.org/sci-news/tyrmut.htm |
Retina International |
TYRP1
tyrosinase-related protein 1 115501 |
Mutations of the Tyrosinase-related Protein 1 Gene
http://www.retina-international.org/sci-news/trp1mut.htm |
Retina International |
TYRP1
tyrosinase-related protein 1 115501 |
Albinism Database
http://albinismdb.med.umn.edu/ |
William S. Oetting, Int. Albinism Centre, Univ. of Minnesota, U.S.A. |
Go Back To Main Index! | ||
UBA1
ubiquitin-like modifier activating enzyme 1 314370 |
UBA1 database at LOVD
http://www.LOVD.nl/UBA1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
UBE2A
ubiquitin-conjugating enzyme E2A (RAD6 homolog) 312180 |
UBE2A database at LOVD
http://www.LOVD.nl/UBE2A |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
UBE2NL
ubiquitin-conjugating enzyme E2N-like |
UBE2NL database at LOVD
http://www.LOVD.nl/UBE2NL |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
UBE3A
ubiquitin protein ligase E3A 601623 |
NGRL, Manchester LOVD
http://ngrl.man.ac.uk/lovd2/home.php?select_db=UBE3A |
Bharathi Kattamuri and Simon Ramsden |
UBQLN2
ubiquilin 2 300264 |
UBQLN2 database at LOVD
http://www.LOVD.nl/UBQLN2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
UNC119
unc-119 homolog (C. elegans) 604011 |
Mutations of HRG4
http://www.retina-international.org/sci-news/hrg4mut.htm |
Retina International |
UNC13D
unc-13 homolog D (C. elegans) 608897 |
UNC13Dbase: Mutation registry for Familial hemophagocytic lymphohistiocytosis 3
http://bioinf.uta.fi/UNC13Dbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
UNC13D
unc-13 homolog D (C. elegans) 608897 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/UNC13D |
Ammar Husami and Theru A. Sivakumaran |
UNG
uracil-DNA glycosylase 191525 |
UNGbase: Mutation registry for UNG deficiency (Hyper-IgM syndrome, type 5)
http://bioinf.uta.fi/UNGbase/ |
Anne Durandy and Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
UPF3B
UPF3 regulator of nonsense transcripts homolog B (yeast) 300298 |
UPF3B database at LOVD
http://www.LOVD.nl/UPF3B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
UPRT
uracil phosphoribosyltransferase (FUR1) homolog (S. cerevisiae) 300656 |
UPRT database at LOVD
http://www.LOVD.nl/UPRT |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
USH1C
Usher syndrome 1C (autosomal recessive, severe) 605242 |
Mutations of the Harmonin Gene
http://www.retina-international.org/sci-news/ush1cmut.htm |
Retina International |
USH1C
Usher syndrome 1C (autosomal recessive, severe) 605242 |
The UMD USH1C mutations database
http://www.umd.be/USH1C/ |
A.-F. Roux and D. Baux |
USH1C
Usher syndrome 1C (autosomal recessive, severe) 605242 |
Retinal and hearing impairment genetic mutation database USH1C
http://www.LOVD.nl/USH1C |
David Baux |
USH1C
Usher syndrome 1C (autosomal recessive, severe) 605242 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=USH1C |
Ammar Husami and Theru A. Sivakumaran |
USH1G
Usher syndrome 1G (autosomal recessive) 607696 |
The UMD USH1G mutations database
http://www.umd.be/USH1G/ |
A.-F. Roux and D. Baux |
USH1G
Usher syndrome 1G (autosomal recessive) 607696 |
Retinal and hearing impairment genetic mutation database USH1G
http://www.LOVD.nl/USH1G |
David Baux |
USH1G
Usher syndrome 1G (autosomal recessive) 607696 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=USH1C |
Ammar Husami and Theru A. Sivakumaran |
USH2A
Usher syndrome 2A (autosomal recessive, mild) 608400 |
Mutations of the USH2a Gene
http://www.retina-international.org/sci-news/ush2amut.htm |
Retina International |
USH2A
Usher syndrome 2A (autosomal recessive, mild) 608400 |
The UMD USH2A mutations database
http://www.umd.be/USH2A/ |
A.-F. Roux and D. Baux |
USH2A
Usher syndrome 2A (autosomal recessive, mild) 608400 |
Retinal and hearing impairment genetic mutation database USH2A
http://www.LOVD.nl/USH2A |
David Baux |
USH2A
Usher syndrome 2A (autosomal recessive, mild) 608400 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
https://research.cchmc.org/LOVD/home.php?select_db=USH2A |
Ammar Husami and Theru A. Sivakumaran |
USP11
ubiquitin specific peptidase 11 300050 |
USP11 database at LOVD
http://www.LOVD.nl/USP11 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
USP26
ubiquitin specific peptidase 26 300309 |
USP26 database at LOVD
http://www.LOVD.nl/USP26 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
USP51
ubiquitin specific peptidase 51 |
USP51 database at LOVD
http://www.LOVD.nl/USP51 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
USP9X
ubiquitin specific peptidase 9, X-linked 300072 |
USP9X database at LOVD
http://www.LOVD.nl/USP9X |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
VAMP7
vesicle-associated membrane protein 7 300053 |
VAMP7 database at LOVD
http://www.LOVD.nl/VAMP7 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
VBP1
von Hippel-Lindau binding protein 1 300133 |
VBP1 database at LOVD
http://www.LOVD.nl/VBP1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
VCP
valosin-containing protein 601023 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/VCP |
Johan T den Dunnen Leiden Univ. Med Centre |
VGLL1
vestigial like 1 (Drosophila) 300583 |
VGLL1 database at LOVD
http://www.LOVD.nl/VGLL1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
VHL
von Hippel-Lindau tumor suppressor 608537 |
The UMD VHL mutations database
http://www.umd.be/VHL/ |
Christophe Beroud, Laboratoire de g�n�tique Mol�culaire et Chromosomique, Montpellier, France |
VIM
vimentin 193060 |
VIM database at LOVD
http://www.LOVD.nl/VIM |
Johan T den Dunnen Leiden Univ. Med Centre |
VMA21
VMA21 vacuolar H+-ATPase homolog (S. cerevisiae) 310440 |
Leiden Muscular Dystrophy pages
http://www.LOVD.nl/VMA21 |
Johan T den Dunnen Leiden Univ. Med Centre |
VSIG1
V-set and immunoglobulin domain containing 1 300620 |
VSIG1 database at LOVD
http://www.LOVD.nl/VSIG1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
VSIG4
V-set and immunoglobulin domain containing 4 300353 |
VSIG4 database at LOVD
http://www.LOVD.nl/VSIG4 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
VWF
von Willebrand factor 193400 |
Von Willebrand Factor Database
http://vwf.group.shef.ac.uk/ |
Dan Hampshire, The University of Sheffield, Sheffield, UK |
VWF
von Willebrand factor 193400 |
VWF Mutation Registry at Hemobase
http://www.vwf.hemobase.com |
Francisco Vidal, Irene Corrales |
Go Back To Main Index! | ||
WAS
Wiskott-Aldrich syndrome (eczema-thrombocytopenia) 300392 |
WASbase: Mutation registry for Wiskott-Aldrich syndrome (WAS)
http://bioinf.uta.fi/WASbase/ |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
WAS
Wiskott-Aldrich syndrome (eczema-thrombocytopenia) 300392 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/WAS |
Ammar Husami and Theru A. Sivakumaran |
WDR13
WD repeat domain 13 300512 |
WDR13 database at LOVD
http://www.LOVD.nl/WDR13 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WDR44
WD repeat domain 44 |
WDR44 database at LOVD
http://www.LOVD.nl/WDR44 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WFS1
Wolfram syndrome 1 (wolframin) 606201 |
Hereditary Hearing Loss Homepage
http://webh01.ua.ac.be/hhh/ |
Guy van Camp Univ. of Antwerp Antwerp, Belgium Richard J.H. Smith Univ. of Iowa Hospitals & Clinics Iowa city, U.S.A |
WFS1
Wolfram syndrome 1 (wolframin) 606201 |
CCHMC - Human Genetics Mutation Database
http://www.LOVD.nl/WFS1 |
Ammar Husami and Theru A. Sivakumaran |
WNK3
WNK lysine deficient protein kinase 3 300358 |
WNK3 database at LOVD
http://www.LOVD.nl/WNK3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WRN
Werner syndrome, RecQ helicase-like 604611 |
Database of WS-associated WRN mutations
http://www.pathology.washington.edu/research/werner/database/ |
International Registry of Werner Syndrome, George M. Martin, Junko Oshima & Dru F. Leistritz, Department of Pathology, University of Washington Seattle, USA |
WWC3
WWC family member 3 |
WWC3 database at LOVD
http://www.LOVD.nl/WWC3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
XG
Xg blood group 314700 |
XG database at LOVD
http://www.LOVD.nl/XG |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
XIAP
X-linked inhibitor of apoptosis 300079 |
XIAP database at LOVD
http://www.LOVD.nl/XIAP |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
XIAP
X-linked inhibitor of apoptosis 300079 |
**PUBLIC** CCHMC Molecular Genetics Laboratory Mutation Database
http://www.LOVD.nl/XIAP |
Ammar Husami and Theru A. Sivakumaran |
XK
X-linked Kx blood group (McLeod syndrome) 314850 |
Blood Group Antigen Mutation Database
http://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/home |
Olga O. Blumenfeld, Dept. of Biochemistry,Santosh Patnaik,Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A |
XK
X-linked Kx blood group (McLeod syndrome) 314850 |
XK database at LOVD
http://www.LOVD.nl/XK |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
XKRX
XK, Kell blood group complex subunit-related, X-linked 300684 |
XKRX database at LOVD
http://www.LOVD.nl/XKRX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
XPNPEP2
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound 300145 |
XPNPEP2 database at LOVD
http://www.LOVD.nl/XPNPEP2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
YY2
YY2 transcription factor 300570 |
YY2 database at LOVD
http://www.LOVD.nl/YY2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
Go Back To Main Index! | ||
ZAP70
zeta-chain (TCR) associated protein kinase 70kDa 176947 |
ZAP70base: Mutation registry for autosomal recessive ZAP70 immunodeficiency
http://bioinf.uta.fi/ZAP70base/index.php |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
ZBED1
zinc finger, BED-type containing 1 300178 |
ZBED1 database at LOVD
http://www.LOVD.nl/ZBED1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZBTB33
zinc finger and BTB domain containing 33 300329 |
ZBTB33 database at LOVD
http://www.LOVD.nl/ZBTB33 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZC3H12B
zinc finger CCCH-type containing 12B |
ZC3H12B database at LOVD
http://www.LOVD.nl/ZC3H12B |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZC4H2
zinc finger, C4H2 domain containing |
ZC4H2 database at LOVD
http://www.LOVD.nl/ZC4H2 |
Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZCCHC13
zinc finger, CCHC domain containing 13 |
ZCCHC13 database at LOVD
http://www.LOVD.nl/ZCCHC13 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZCCHC5
zinc finger, CCHC domain containing 5 |
ZCCHC5 database at LOVD
http://www.LOVD.nl/ZCCHC5 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZDHHC9
zinc finger, DHHC-type containing 9 300646 |
ZDHHC9 database at LOVD
http://www.LOVD.nl/ZDHHC9 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZFX
zinc finger protein, X-linked 314980 |
ZFX database at LOVD
http://www.LOVD.nl/ZFX |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZMAT1
zinc finger, matrin type 1 |
ZMAT1 database at LOVD
http://www.LOVD.nl/ZMAT1 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZMPSTE24
zinc metallopeptidase (STE24 homolog, S. cerevisiae) 606480 |
Leiden Muscular Dystrophy Pages
http://www.LOVD.nl/ZMPSTE24 |
Johan T. den Dunnen Leiden Univ.Med Centre, Leiden, The Netherlands |
ZMYM3
zinc finger, MYM-type 3 300061 |
ZMYM3 database at LOVD
http://www.LOVD.nl/ZMYM3 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF182
zinc finger protein 182 314993 |
ZNF182 database at LOVD
http://www.LOVD.nl/ZNF182 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF185
zinc finger protein 185 (LIM domain) 300381 |
ZNF185 database at LOVD
http://www.LOVD.nl/ZNF185 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF280C
zinc finger protein 280C |
ZNF280C database at LOVD
http://www.LOVD.nl/ZNF280C |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF41
zinc finger protein 41 314995 |
ZNF41 database at LOVD
http://www.LOVD.nl/ZNF41 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF449
zinc finger protein 449 300627 |
ZNF449 database at LOVD
http://www.LOVD.nl/ZNF449 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF630
zinc finger protein 630 |
ZNF630 database at LOVD
http://www.LOVD.nl/ZNF630 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF645
zinc finger protein 645 |
ZNF645 database at LOVD
http://www.LOVD.nl/ZNF645 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF673
zinc finger family member 673 300585 |
ZNF673 database at LOVD
http://www.LOVD.nl/ZNF673 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF711
zinc finger protein 711 314990 |
ZNF711 database at LOVD
http://www.LOVD.nl/ZNF711 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZNF75D
zinc finger protein 75D 314997 |
Mental Retardation database
http://www.LOVD.nl/ZNF75D |
Ing. Ivo F.A.C. Fokkema |
ZNF81
zinc finger protein 81 314998 |
ZNF81 database at LOVD
http://www.LOVD.nl/ZNF81 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZRSR2
zinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 300028 |
ZRSR2 database at LOVD
http://www.LOVD.nl/ZRSR2 |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
ZXDA
zinc finger, X-linked, duplicated A 300235 |
ZXDA database at LOVD
http://www.LOVD.nl/ZXDA |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
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