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Browse Genes by Name - A

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