Catabolic process
- AASS: aminoadipate-semialdehyde synthase
- ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
- ABHD5: abhydrolase domain containing 5
- ACAD8: acyl-CoA dehydrogenase family, member 8
- ACADM: acyl-CoA dehydrogenase, C-4 to C-12 straight chain
- ACADS: acyl-CoA dehydrogenase, C-2 to C-3 short chain
- ACADSB: acyl-CoA dehydrogenase, short/branched chain
- ACADVL: acyl-CoA dehydrogenase, very long chain
- ACAN: aggrecan
- ACAT1: acetyl-CoA acetyltransferase 1
- ACSF3: acyl-CoA synthetase family member 3
- ADA: adenosine deaminase
- ADAMTS13: ADAM metallopeptidase with thrombospondin type 1 motif, 13
- AGL: amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase
- AGXT: alanine-glyoxylate aminotransferase
- AKT1: v-akt murine thymoma viral oncogene homolog 1
- ALDH4A1: aldehyde dehydrogenase 4 family, member A1
- ALDH5A1: aldehyde dehydrogenase 5 family, member A1
- ALDH7A1: aldehyde dehydrogenase 7 family, member A1
- ALDOB: aldolase B, fructose-bisphosphate
- ALS2: amyotrophic lateral sclerosis 2 (juvenile)
- APC: adenomatous polyposis coli
- APOE: apolipoprotein E
- ARG1: arginase 1
- ARSB: arylsulfatase B
- ASL: argininosuccinate lyase
- ASPA: aspartoacylase
- ATG16L1: autophagy related 16-like 1 (S. cerevisiae)
- ATL1: atlastin GTPase 1
- ATM: ataxia telangiectasia mutated
- ATP2A1: ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
- ATP8B1: ATPase, aminophospholipid transporter, class I, type 8B, member 1
- ATXN3: ataxin 3
- AUH: AU RNA binding protein/enoyl-CoA hydratase
- BARD1: BRCA1 associated RING domain 1
- BCKDHA: branched chain keto acid dehydrogenase E1, alpha polypeptide
- BCKDHB: branched chain keto acid dehydrogenase E1, beta polypeptide
- BLM: Bloom syndrome, RecQ helicase-like
- BSCL2: Berardinelli-Seip congenital lipodystrophy 2 (seipin)
- CBS: cystathionine-beta-synthase
- CDKL5: cyclin-dependent kinase-like 5
- CHEK2: checkpoint kinase 2
- CISD2: CDGSH iron sulfur domain 2
- CLN3: ceroid-lipofuscinosis, neuronal 3
- COLQ: collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
- CPS1: carbamoyl-phosphate synthase 1, mitochondrial
- CPT2: carnitine palmitoyltransferase 2
- CST3: cystatin C
- DBT: dihydrolipoamide branched chain transacylase E2
- DCN: decorin
- DLD: dihydrolipoamide dehydrogenase
- DNM2: dynamin 2
- DPYD: dihydropyrimidine dehydrogenase
- ELANE: elastase, neutrophil expressed
- ERBB2: v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian)
- ERCC2: excision repair cross-complementing rodent repair deficiency, complementation group 2
- ERCC3: excision repair cross-complementing rodent repair deficiency, complementation group 3
- ERCC8: excision repair cross-complementing rodent repair deficiency, complementation group 8
- ETFDH: electron-transferring-flavoprotein dehydrogenase
- ETHE1: ethylmalonic encephalopathy 1
- FAH: fumarylacetoacetate hydrolase (fumarylacetoacetase)
- FGD1: FYVE, RhoGEF and PH domain containing 1
- FGD4: FYVE, RhoGEF and PH domain containing 4
- FGF23: fibroblast growth factor 23
- FLNA: filamin A, alpha
- FOXL2: forkhead box L2
- FTCD: formiminotransferase cyclodeaminase
- FUCA1: fucosidase, alpha-L- 1, tissue
- G6PD: glucose-6-phosphate dehydrogenase
- GAA: glucosidase, alpha; acid
- GALE: UDP-galactose-4-epimerase
- GALK1: galactokinase 1
- GALNS: galactosamine (N-acetyl)-6-sulfate sulfatase
- GALT: galactose-1-phosphate uridylyltransferase
- GBA: glucosidase, beta, acid
- GCDH: glutaryl-CoA dehydrogenase
- GCH1: GTP cyclohydrolase 1
- GLA: galactosidase, alpha
- GLB1: galactosidase, beta 1
- GM2A: GM2 ganglioside activator
- GNS: glucosamine (N-acetyl)-6-sulfatase
- GPC3: glypican 3
- GUSB: glucuronidase, beta
- HADH: hydroxyacyl-CoA dehydrogenase
- HADHA: hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
- HADHB: hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
- HAL: histidine ammonia-lyase
- HBA2: hemoglobin, alpha 2
- HBB: hemoglobin, beta
- HEXA: hexosaminidase A (alpha polypeptide)
- HEXB: hexosaminidase B (beta polypeptide)
- HGD: homogentisate 1,2-dioxygenase
- HGSNAT: heparan-alpha-glucosaminide N-acetyltransferase
- HMGCL: 3-hydroxymethyl-3-methylglutaryl-CoA lyase
- HPD: 4-hydroxyphenylpyruvate dioxygenase
- HPRT1: hypoxanthine phosphoribosyltransferase 1
- HPSE2: heparanase 2
- HRAS: v-Ha-ras Harvey rat sarcoma viral oncogene homolog
- HSD17B10: hydroxysteroid (17-beta) dehydrogenase 10
- IDS: iduronate 2-sulfatase
- IDUA: iduronidase, alpha-L-
- INS: insulin
- IVD: isovaleryl-CoA dehydrogenase
- LDHA: lactate dehydrogenase A
- LDLR: low density lipoprotein receptor
- LIPH: lipase, member H
- LPL: lipoprotein lipase
- LRP5: low density lipoprotein receptor-related protein 5
- LRRK2: leucine-rich repeat kinase 2
- MAPT: microtubule-associated protein tau
- MCCC1: methylcrotonoyl-CoA carboxylase 1 (alpha)
- MCCC2: methylcrotonoyl-CoA carboxylase 2 (beta)
- MCEE: methylmalonyl CoA epimerase
- MLH1: mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
- MLYCD: malonyl-CoA decarboxylase
- MMAA: methylmalonic aciduria (cobalamin deficiency) cblA type
- MSH2: mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
- MSH6: mutS homolog 6 (E. coli)
- MT-ATP6: mitochondrially encoded ATP synthase 6
- MTMR2: myotubularin related protein 2
- MUT: methylmalonyl CoA mutase
- MUTYH: mutY homolog (E. coli)
- MYBPC3: myosin binding protein C, cardiac
- MYH7: myosin, heavy chain 7, cardiac muscle, beta
- MYH9: myosin, heavy chain 9, non-muscle
- NAGA: N-acetylgalactosaminidase, alpha-
- NAGLU: N-acetylglucosaminidase, alpha
- NCF1: neutrophil cytosolic factor 1
- NF1: neurofibromin 1
- NHLRC1: NHL repeat containing 1
- NPC1: Niemann-Pick disease, type C1
- NTRK1: neurotrophic tyrosine kinase, receptor, type 1
- OCRL: oculocerebrorenal syndrome of Lowe
- OPA1: optic atrophy 1 (autosomal dominant)
- OXCT1: 3-oxoacid CoA transferase 1
- PAFAH1B1: platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
- PAH: phenylalanine hydroxylase
- PARK2: parkinson protein 2, E3 ubiquitin protein ligase (parkin)
- PCBD1: pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
- PCCA: propionyl CoA carboxylase, alpha polypeptide
- PCCB: propionyl CoA carboxylase, beta polypeptide
- PCSK9: proprotein convertase subtilisin/kexin type 9
- PGAM2: phosphoglycerate mutase 2 (muscle)
- PGK1: phosphoglycerate kinase 1
- PHKA1: phosphorylase kinase, alpha 1 (muscle)
- PHKA2: phosphorylase kinase, alpha 2 (liver)
- PHKB: phosphorylase kinase, beta
- PHKG2: phosphorylase kinase, gamma 2 (testis)
- PHYH: phytanoyl-CoA 2-hydroxylase
- PINK1: PTEN induced putative kinase 1
- PKLR: pyruvate kinase, liver and RBC
- PML: promyelocytic leukemia
- PMS2: PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
- PNP: purine nucleoside phosphorylase
- PNPLA2: patatin-like phospholipase domain containing 2
- PPT1: palmitoyl-protein thioesterase 1
- PRICKLE1: prickle homolog 1 (Drosophila)
- PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
- PRODH: proline dehydrogenase (oxidase) 1
- PTEN: phosphatase and tensin homolog
- PYGL: phosphorylase, glycogen, liver
- PYGM: phosphorylase, glycogen, muscle
- QDPR: quinoid dihydropteridine reductase
- RAB23: RAB23, member RAS oncogene family
- RAB7A: RAB7A, member RAS oncogene family
- RASA1: RAS p21 protein activator (GTPase activating protein) 1
- RBM8A: RNA binding motif protein 8A
- RNASEH2A: ribonuclease H2, subunit A
- RNASEH2B: ribonuclease H2, subunit B
- RNASEH2C: ribonuclease H2, subunit C
- RP2: retinitis pigmentosa 2 (X-linked recessive)
- RPL11: ribosomal protein L11
- RPL35A: ribosomal protein L35a
- RPL5: ribosomal protein L5
- RPS10: ribosomal protein S10
- RPS17: ribosomal protein S17
- RPS19: ribosomal protein S19
- RPS24: ribosomal protein S24
- RPS26: ribosomal protein S26
- RPS7: ribosomal protein S7
- RYR2: ryanodine receptor 2 (cardiac)
- SAR1B: SAR1 homolog B (S. cerevisiae)
- SEPT9: septin 9
- SGSH: N-sulfoglucosamine sulfohydrolase
- SMAD3: SMAD family member 3
- SMAD4: SMAD family member 4
- SOD1: superoxide dismutase 1, soluble
- SOS1: son of sevenless homolog 1 (Drosophila)
- SQSTM1: sequestosome 1
- TAF1: TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
- TAT: tyrosine aminotransferase
- TGFB1: transforming growth factor, beta 1
- TNNI3: troponin I type 3 (cardiac)
- TNNT2: troponin T type 2 (cardiac)
- TPM2: tropomyosin 2 (beta)
- TSC1: tuberous sclerosis 1
- TWIST1: twist basic helix-loop-helix transcription factor 1
- TYMP: thymidine phosphorylase
- UBE3A: ubiquitin protein ligase E3A
- UGT1A1: UDP glucuronosyltransferase 1 family, polypeptide A1
- VCAN: versican
- VCP: valosin containing protein
- WFS1: Wolfram syndrome 1 (wolframin)
- WRN: Werner syndrome, RecQ helicase-like
- XPA: xeroderma pigmentosum, complementation group A
- XPC: xeroderma pigmentosum, complementation group C
Source: Gene Ontology Consortium
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