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Hydrolase activity

Hydrolase activity

  • ABCB7: ATP-binding cassette, sub-family B (MDR/TAP), member 7
  • ABCC2: ATP-binding cassette, sub-family C (CFTR/MRP), member 2
  • ABCC6: ATP-binding cassette, sub-family C (CFTR/MRP), member 6
  • ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
  • ADA: adenosine deaminase
  • ADAMTS2: ADAM metallopeptidase with thrombospondin type 1 motif, 2
  • AGA: aspartylglucosaminidase
  • AHCY: adenosylhomocysteinase
  • AMPD1: adenosine monophosphate deaminase 1 (isoform M)
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • APTX: aprataxin
  • ARG1: arginase, liver
  • ARSA: arylsulfatase A
  • ASPA: aspartoacylase (Canavan disease)
  • ATP1A2: ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide
  • ATP1A3: ATPase, Na+/K+ transporting, alpha 3 polypeptide
  • ATP2A2: ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
  • ATP2B2: ATPase, Ca++ transporting, plasma membrane 2
  • ATP7A: ATPase, Cu++ transporting, alpha polypeptide
  • ATP7B: ATPase, Cu++ transporting, beta polypeptide
  • ATRX: alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
  • BLM: Bloom syndrome, RecQ helicase-like
  • BRIP1: BRCA1 interacting protein C-terminal helicase 1
  • CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
  • DIRAS3: DIRAS family, GTP-binding RAS-like 3
  • DNM2: dynamin 2
  • EPM2A: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
  • ERAP1: endoplasmic reticulum aminopeptidase 1
  • ERCC6: excision repair cross-complementing rodent repair deficiency, complementation group 6
  • EYA1: eyes absent homolog 1 (Drosophila)
  • F2: coagulation factor II (thrombin)
  • F9: coagulation factor IX
  • FAH: fumarylacetoacetate hydrolase (fumarylacetoacetase)
  • FUCA1: fucosidase, alpha-L- 1, tissue
  • GCH1: GTP cyclohydrolase 1
  • GLA: galactosidase, alpha
  • GNAS: GNAS complex locus
  • HEXB: hexosaminidase B (beta polypeptide)
  • IDS: iduronate 2-sulfatase
  • IDUA: iduronidase, alpha-L-
  • KIF1B: kinesin family member 1B
  • LPL: lipoprotein lipase
  • MAN2B1: mannosidase, alpha, class 2B, member 1
  • MANBA: mannosidase, beta A, lysosomal
  • MMP20: matrix metallopeptidase 20
  • MSH2: mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
  • MSH6: mutS homolog 6 (E. coli)
  • MT-ATP6: mitochondrially encoded ATP synthase 6
  • MTM1: myotubularin 1
  • MTMR2: myotubularin related protein 2
  • MUTYH: mutY homolog (E. coli)
  • MYH7: myosin, heavy chain 7, cardiac muscle, beta
  • MYO6: myosin VI
  • MYO7A: myosin VIIA
  • NCF1: neutrophil cytosolic factor 1
  • OCRL: oculocerebrorenal syndrome of Lowe
  • OPA1: optic atrophy 1 (autosomal dominant)
  • PCSK9: proprotein convertase subtilisin/kexin type 9
  • PROC: protein C (inactivator of coagulation factors Va and VIIIa)
  • PSEN1: presenilin 1
  • PTEN: phosphatase and tensin homolog
  • PTPN11: protein tyrosine phosphatase, non-receptor type 11
  • RAB7A: RAB7A, member RAS oncogene family
  • RAD50: RAD50 homolog (S. cerevisiae)
  • RAD51: RAD51 homolog (RecA homolog, E. coli) (S. cerevisiae)
  • RECQL4: RecQ protein-like 4
  • SEPT9: septin 9
  • SETX: senataxin
  • SMARCAL1: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
  • SMC1A: structural maintenance of chromosomes 1A
  • SMC3: structural maintenance of chromosomes 3
  • SMPD1: sphingomyelin phosphodiesterase 1, acid lysosomal
  • SPAST: spastin
  • SPG7: spastic paraplegia 7 (pure and complicated autosomal recessive)
  • TMPRSS3: transmembrane protease, serine 3
  • TOR1A: torsin family 1, member A (torsin A)
  • UCHL1: ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
  • USP9Y: ubiquitin specific peptidase 9, Y-linked
  • VCP: valosin-containing protein
  • WRN: Werner syndrome, RecQ helicase-like

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference. (June 2009).

 
Published: November 20, 2009