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Browse Genes by Symbol - A

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  • 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

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