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Browse Genes by Symbol - A
A | B | C | D-E | F | G | H-K | L | M | N-O | P | Q-S | T-V | W-Z || All
- ABCC6:ATP-binding cassette, sub-family C (CFTR/MRP), member 6
- ADAMTS2:a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2
- AGXT:alanine-glyoxylate aminotransferase (oxalosis I; hyperoxaluria I; glycolicaciduria; serine-pyruvate aminotransferase)
- ALAD:aminolevulinate, delta-, dehydratase
- ALAS1:aminolevulinate, delta-, synthase 1
- ALAS2:aminolevulinate, delta-, synthase 2 (sideroblastic/hypochromic anemia)
- ALMS1:Alstrom syndrome 1
- ALS2:amyotrophic lateral sclerosis 2 (juvenile)
- APOE:apolipoprotein E
- APP:amyloid beta (A4) precursor protein (protease nexin-II, Alzheimer disease)
- AR:androgen receptor (dihydrotestosterone receptor; testicular feminization; spinal and bulbar muscular atrophy; Kennedy disease)
- ARHI:ras homolog gene family, member I
- ASPA:aspartoacylase (aminoacylase 2, Canavan disease)
- ATM:ataxia telangiectasia mutated (includes complementation groups A, C and D)
- ATP7A:ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)
- ATP7B:ATPase, Cu++ transporting, beta polypeptide (Wilson disease)
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Published: October 8, 2004