Hydrolase activity
- ABCA3: ATP-binding cassette, sub-family A (ABC1), member 3
- ABCB11: ATP-binding cassette, sub-family B (MDR/TAP), member 11
- ABCB4: ATP-binding cassette, sub-family B (MDR/TAP), member 4
- ABCB7: ATP-binding cassette, sub-family B (MDR/TAP), member 7
- ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
- ABCG5: ATP-binding cassette, sub-family G (WHITE), member 5
- ABCG8: ATP-binding cassette, sub-family G (WHITE), member 8
- ADA: adenosine deaminase
- ADAMTS13: ADAM metallopeptidase with thrombospondin type 1 motif, 13
- ADAMTS2: ADAM metallopeptidase with thrombospondin type 1 motif, 2
- AGA: aspartylglucosaminidase
- AGL: amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
- AHCY: adenosylhomocysteinase
- ALPL: alkaline phosphatase, liver/bone/kidney
- ANG: angiogenin, ribonuclease, RNase A family, 5
- APTX: aprataxin
- ARG1: arginase 1
- ARSA: arylsulfatase A
- ARSB: arylsulfatase B
- ARSE: arylsulfatase E (chondrodysplasia punctata 1)
- ASAH1: N-acylsphingosine amidohydrolase (acid ceramidase) 1
- ASPA: aspartoacylase
- ATL1: atlastin GTPase 1
- ATP1A2: ATPase, Na+/K+ transporting, alpha 2 polypeptide
- ATP1A3: ATPase, Na+/K+ transporting, alpha 3 polypeptide
- ATP2A1: ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
- 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
- ATP8B1: ATPase, aminophospholipid transporter, class I, type 8B, member 1
- ATRX: alpha thalassemia/mental retardation syndrome X-linked
- ATXN3: ataxin 3
- BCHE: butyrylcholinesterase
- BLM: Bloom syndrome, RecQ helicase-like
- BRIP1: BRCA1 interacting protein C-terminal helicase 1
- C10orf2: chromosome 10 open reading frame 2
- CAPN3: calpain 3, (p94)
- CASR: calcium-sensing receptor
- CFTR: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
- CTDP1: CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
- CTSA: cathepsin A
- CYLD: cylindromatosis (turban tumor syndrome)
- DICER1: dicer 1, ribonuclease type III
- DNAH5: dynein, axonemal, heavy chain 5
- DNM2: dynamin 2
- DYNC1H1: dynein, cytoplasmic 1, heavy chain 1
- ELANE: elastase, neutrophil expressed
- EPM2A: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
- ERAP1: endoplasmic reticulum aminopeptidase 1
- ERCC2: excision repair cross-complementing rodent repair deficiency, complementation group 2
- ERCC3: excision repair cross-complementing rodent repair deficiency, complementation group 3
- ERCC6: excision repair cross-complementing rodent repair deficiency, complementation group 6
- EYA1: eyes absent homolog 1 (Drosophila)
- F12: coagulation factor XII (Hageman factor)
- F2: coagulation factor II (thrombin)
- FAH: fumarylacetoacetate hydrolase (fumarylacetoacetase)
- FIG4: FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
- FUCA1: fucosidase, alpha-L- 1, tissue
- G6PC: glucose-6-phosphatase, catalytic subunit
- GAA: glucosidase, alpha; acid
- GALNS: galactosamine (N-acetyl)-6-sulfate sulfatase
- GBA: glucosidase, beta, acid
- GCH1: GTP cyclohydrolase 1
- GLA: galactosidase, alpha
- GLB1: galactosidase, beta 1
- GNAI3: guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3
- GNAS: GNAS complex locus
- GNAT2: guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
- GNPAT: glyceronephosphate O-acyltransferase
- GNS: glucosamine (N-acetyl)-6-sulfatase
- GUSB: glucuronidase, beta
- HPSE2: heparanase 2
- HTRA1: HtrA serine peptidase 1
- IDS: iduronate 2-sulfatase
- IGHMBP2: immunoglobulin mu binding protein 2
- KIF1B: kinesin family member 1B
- KL: klotho
- LCT: lactase
- LIPA: lipase A, lysosomal acid, cholesterol esterase
- LIPH: lipase, member H
- LPIN2: lipin 2
- LPL: lipoprotein lipase
- LRRK2: leucine-rich repeat kinase 2
- MCM6: minichromosome maintenance complex component 6
- MLH1: mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
- 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
- MYH3: myosin, heavy chain 3, skeletal muscle, embryonic
- MYH7: myosin, heavy chain 7, cardiac muscle, beta
- MYH9: myosin, heavy chain 9, non-muscle
- MYO6: myosin VI
- MYO7A: myosin VIIA
- NAGA: N-acetylgalactosaminidase, alpha-
- NBN: nibrin
- NCF1: neutrophil cytosolic factor 1
- NEU1: sialidase 1 (lysosomal sialidase)
- OCRL: oculocerebrorenal syndrome of Lowe
- OPA1: optic atrophy 1 (autosomal dominant)
- PARK7: parkinson protein 7
- PCSK9: proprotein convertase subtilisin/kexin type 9
- PDP1: pyruvate dehydrogenase phosphatase catalytic subunit 1
- PEPD: peptidase D
- PEX1: peroxisomal biogenesis factor 1
- PLA2G6: phospholipase A2, group VI (cytosolic, calcium-independent)
- PLCB4: phospholipase C, beta 4
- PLG: plasminogen
- PMS2: PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
- PNPLA2: patatin-like phospholipase domain containing 2
- PPT1: palmitoyl-protein thioesterase 1
- PROC: protein C (inactivator of coagulation factors Va and VIIIa)
- PRSS1: protease, serine, 1 (trypsin 1)
- PSEN1: presenilin 1
- PSEN2: presenilin 2 (Alzheimer disease 4)
- PTEN: phosphatase and tensin homolog
- PTPN11: protein tyrosine phosphatase, non-receptor type 11
- PTPN22: protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
- RAB23: RAB23, member RAS oncogene family
- RAB7A: RAB7A, member RAS oncogene family
- RAD50: RAD50 homolog (S. cerevisiae)
- RAD51: RAD51 homolog (S. cerevisiae)
- RECQL4: RecQ protein-like 4
- REN: renin
- RNASEH2A: ribonuclease H2, subunit A
- SALL1: sal-like 1 (Drosophila)
- SAR1B: SAR1 homolog B (S. cerevisiae)
- SEPT9: septin 9
- SETX: senataxin
- SI: sucrase-isomaltase (alpha-glucosidase)
- SMARCA4: SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
- 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
- SPAST: spastin
- SPG7: spastic paraplegia 7 (pure and complicated autosomal recessive)
- TMPRSS3: transmembrane protease, serine 3
- TNNT2: troponin T type 2 (cardiac)
- TOR1A: torsin family 1, member A (torsin A)
- TREX1: three prime repair exonuclease 1
- 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 Consortium
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