A (132) | B (54) | C (205) | D (45) | E (30) | F (80) | G (88) | H (109) | I (76) | J (9) | K (51) | L (35) | M (124) | N (53) | O (17) | P (143) | Q (1) | R (69) | S (130) | T (112) | U (26) | V (12) | W (12) | X (7) | Y (1) | Z (25)
HGNC GENE SYMBOLsort descending HGNC gene description OMIM NO DATABASE NAME/INTERNET ADDRESS CURATORS
FOXL2 forkhead box L2 605597 The Human FOXL2 Allelic Variant Database Diane Beysen, Elfride de Baere, Centre for Medical Genetics, Gent, Belgium
FAS Fas (TNF receptor superfamily, member 6) 134637 Autoimmune Lymphoproliferative Syndrome Database (ALPSbase): Database of mutations causing human 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 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) Mauno Vihinen, Univ. of Tampere, Tampere, Finland
FASLG Fas ligand (TNF superfamily, member 6) 134638 CCHMC - Human Genetics Mutation Database Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran
FOXN1 forkhead box N1 600838 FOXN1base: Mutation registry for T-cell immunodeficiency, congenital alopecia, and nail dystrophy (Previously known as WHNbase) Mauno Vihinen & Claudio Pignata, Univ. of Tampere, Tampere, Finland
FTSJ1 FtsJ homolog 1 (E. coli) 300499 FTSJ1 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM3A family with sequence similarity 3, member A 300492 FAM3A database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM120C family with sequence similarity 120C 300741 FAM120C database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FKRP fukutin related protein 606596 Leiden Muscular Dystrophy Pages Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands & Rosário dos Santos, Centro de Genética Médica J., Magalhães, INSA, Portugal
FKBP10 FK506 binding protein 10, 65 kDa 607063 Database of osteogenesis imperfecta and Ehlers-Danlos syndrome variants Raymond Dalgleish, Leicester, UK.
FAM9A family with sequence similarity 9, member A 300477 FAM9A database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM9C family with sequence similarity 9, member C 300479 FAM9C database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM50A family with sequence similarity 50, member A 300453 FAM50A database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FANCL Fanconi anemia, complementation group L 608111 Fanconi Anaemia Mutation Database 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 Arleen Auerbach, Rockefeller University, New York, USA
FATE1 fetal and adult testis expressed 1 300450 FATE1 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM122C family with sequence similarity 122C \N FAM122C database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM47C family with sequence similarity 47, member C \N FAM47C database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FANCI Fanconi anemia, complementation group I 611360 Fanconi Anaemia Mutation Database Arleen D. Auerbach, PhD, The Rockefeller University, NY; Detlev Schindler,MD,PhD, University of Wuerzburg, Germany and consortium
FMR1NB fragile X mental retardation 1 neighbor \N FMR1NB database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAAH2 fatty acid amide hydrolase 2 300654 FAAH2 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM47B family with sequence similarity 47, member B \N FAM47B database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM133A family with sequence similarity 133, member A \N FAM133A database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM123B family with sequence similarity 123B 300647 FAM123B database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FLCN folliculin 607273 Folliculin (FLCN) variation database 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 Database Administration
FAM46D family with sequence similarity 46, member D \N FAM46D database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FUNDC1 FUN14 domain containing 1 \N FUNDC1 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FRMPD4 FERM and PDZ domain containing 4 \N FRMPD4 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FRMPD3 FERM and PDZ domain containing 3 \N FRMPD3 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM47A family with sequence similarity 47, member A \N FAM47A database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FOXR2 forkhead box R2 \N FOXR2 database at LOVD Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy
FAM122B family with sequence similarity 122B \N FAM122B database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM155B family with sequence similarity 155, member B \N FAM155B database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FAM45B family with sequence similarity 45, member B \N FAM45B database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
F12 coagulation factor XII (Hageman factor) 610619 F12base: Mutation registry for Hereditary angioedema type III Mauno Vihinen, Univ. of Tampere, Tampere, Finland
F8 coagulation factor VIII, procoagulant component 306700 The Haemophilia A Mutation, Structure, Test & Resource Site (HAMSTeRS) Dr Geoffrey Kemball-Cook
F8 coagulation factor VIII, procoagulant component 306700 F8 database at LOVD 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 Francisco Vidal, Lorena Ramirez
F9 coagulation factor IX 300746 Haemophilia B Mutation Database P.M Green, F. Giannelli, Division of Genetics & Development, 7th Floor Guys Tower, GKT School of Medicine, Guy's Hospital London SE1 9RT Unitd Kingdom and consortium
F9 coagulation factor IX 300746 F9 database at LOVD Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
F9 coagulation factor IX 300746 F9 Mutation Registry at Hemobase Francisco Vidal, Lorena Ramirez
FANCA Fanconi anemia, complementation group A 607139 Fanconi Anaemia Mutation Database 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 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 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 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 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 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 Arleen D. Auerbach, PhD, The Rockefeller University, NY; Detlev Schindler,MD,PhD, University of Wuerzburg, Germany and consortium
FBN1 fibrillin 1 134797 The UMD FBN1 mutations database Gwenaelle Collod-Beroud, Laboratoire de génétique Moléculaire et Chromosomique, Montpellier, France
FBN2 fibrillin 2 612570 The UMD FBN2 mutations database G. Collod-Béroud
FCGR1A Fc fragment of IgG, high affinity Ia, receptor (CD64) 146760 FCGR1Abase: Mutation registry for CD64 deficiency 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 Mauno Vihinen, Univ. of Tampere, Tampere, Finland
FKTN fukutin 607440 FCMD - Fukuyama type congenital muscular dystrophy Johan T. den Dunnen, Leiden Univ. Med Centre, Leiden, The Netherlands & Rosário dos Santos, Centro de Genética Médica J., Magalhães, INSA, Portugal
FGA fibrinogen alpha chain 134820 A Database For Human Fibrinogen Variants Michel Hanss, Laboratoire d’hématologie, Hospices Civils de Lyon, France
FGB fibrinogen beta chain 134830 A Database For Human Fibrinogen Variants Michel Hanss, Laboratoire d’hématologie, Hospices Civils de Lyon, France
FGD1 FYVE, RhoGEF and PH domain containing 1 300546 FGD1 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FGG fibrinogen gamma chain 134850 A Database For Human Fibrinogen Variants Michel Hanss, Laboratoire d’hématologie, Hospices Civils de Lyon, France
FH fumarate hydratase 136850 TCA Cycle Gene Mutation Database -FH Jean-Pierre Bayley, LUMC, Leiden
FHL1 four and a half LIM domains 1 300163 Leiden Muscular Dystrophy Pages 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 Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FLNA filamin A, alpha 300017 Filamin A, alpha (FLNA) Mental Retardation Database Johan T. den Dunnen Leiden Univ. Med Centre, Leiden, The Netherlands
FLNC filamin C, gamma 102565 Leiden Muscular Dystrophy pages 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 Belinda Giardine and Joseph Borg
FMO3 flavin containing monooxygenase 3 136132 The Homo sapients FMO3 Allelic Variant Database 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 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 Retina International
FTHL17 ferritin, heavy polypeptide-like 17 300308 FTHL17 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FUS fused in sarcoma 137070 Alzheimer Disease & Frontotemporal Dementia Mutation Database Marc Cruts & Nathalie Brouwers Molecular Genetics Department Flanders Interuniversity Institute for Biotechnology (VIB) University of Antwerp (UA), Belgium
FUT1 fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group) 211100 Blood Group Antigen Mutation Database 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 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 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 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 Olga O. Blumenfeld, Dept. of Biochemistry, Santosh Patnaik, Dept. of Cell Biology, Albert Einstein College of Medicine, New York, NY. U.S.A
FOXP3 forkhead box P3 300292 FOXP3 database at LOVD Jacopo Celli and Johan den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FOXP3 forkhead box P3 300292 CCHMC - Human Genetics Mutation Database Ammar Husami, Brian Richardson, Edita Freeman, Kerry Shooner, Thedia Jacobs and Theru A. Sivakumaran
FOXP3 forkhead box P3 300292 FOXP3base: Mutation registry for Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked; IPEX Mauno Vihinen, Univ. of Tampere, Tampere, Finland
FOXO4 forkhead box O4 300033 FOXO4 database at LOVD Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy
FRMD7 FERM domain containing 7 300628 FRMD7 database at LOVD Jacopo Celli Leiden Univ. Med Centre (acting), Curator vacancy

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