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Catabolic process

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 ConsortiumThis link leads to a site outside Genetics Home Reference..

 
Published: May 13, 2013