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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
  • ACE: angiotensin I converting enzyme
  • ACOX1: acyl-CoA oxidase 1, palmitoyl
  • 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
  • AKR1D1: aldo-keto reductase family 1, member D1
  • 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
  • AMACR: alpha-methylacyl-CoA racemase
  • AMT: aminomethyltransferase
  • APC: adenomatous polyposis coli
  • APOA1: apolipoprotein A-I
  • APOE: apolipoprotein E
  • ARG1: arginase 1
  • ARSB: arylsulfatase B
  • ASL: argininosuccinate lyase
  • ASPA: aspartoacylase
  • ATG16L1: autophagy related 16-like 1
  • ATM: ATM serine/threonine kinase
  • ATXN3: ataxin 3
  • AUH: AU RNA binding protein/enoyl-CoA hydratase
  • BCHE: butyrylcholinesterase
  • BCKDHA: branched chain keto acid dehydrogenase E1, alpha polypeptide
  • BCKDHB: branched chain keto acid dehydrogenase E1, beta polypeptide
  • BSCL2: Berardinelli-Seip congenital lipodystrophy 2 (seipin)
  • C9orf72: chromosome 9 open reading frame 72
  • CAT: catalase
  • CAV3: caveolin 3
  • CBS: cystathionine-beta-synthase
  • CDC6: cell division cycle 6
  • CDKN1B: cyclin-dependent kinase inhibitor 1B (p27, Kip1)
  • CEBPA: CCAAT/enhancer binding protein (C/EBP), alpha
  • CECR1: cat eye syndrome chromosome region, candidate 1
  • CHEK2: checkpoint kinase 2
  • CHST3: carbohydrate (chondroitin 6) sulfotransferase 3
  • CISD2: CDGSH iron sulfur domain 2
  • CLN3: ceroid-lipofuscinosis, neuronal 3
  • CLN5: ceroid-lipofuscinosis, neuronal 5
  • CLN6: ceroid-lipofuscinosis, neuronal 6, late infantile, variant
  • CLN8: ceroid-lipofuscinosis, neuronal 8
  • CLPP: caseinolytic mitochondrial matrix peptidase proteolytic subunit
  • COL11A1: collagen, type XI, alpha 1
  • COL11A2: collagen, type XI, alpha 2
  • COL17A1: collagen, type XVII, alpha 1
  • COL18A1: collagen, type XVIII, alpha 1
  • COL1A1: collagen, type I, alpha 1
  • COL1A2: collagen, type I, alpha 2
  • COL2A1: collagen, type II, alpha 1
  • COL3A1: collagen, type III, alpha 1
  • COL4A1: collagen, type IV, alpha 1
  • COL4A3: collagen, type IV, alpha 3 (Goodpasture antigen)
  • COL4A4: collagen, type IV, alpha 4
  • COL4A5: collagen, type IV, alpha 5
  • COL5A1: collagen, type V, alpha 1
  • COL5A2: collagen, type V, alpha 2
  • COL6A1: collagen, type VI, alpha 1
  • COL6A2: collagen, type VI, alpha 2
  • COL6A3: collagen, type VI, alpha 3
  • COL7A1: collagen, type VII, alpha 1
  • COL8A2: collagen, type VIII, alpha 2
  • COL9A1: collagen, type IX, alpha 1
  • COL9A2: collagen, type IX, alpha 2
  • COL9A3: collagen, type IX, alpha 3
  • COLQ: collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
  • CPS1: carbamoyl-phosphate synthase 1, mitochondrial
  • CPT1A: carnitine palmitoyltransferase 1A (liver)
  • CST3: cystatin C
  • CTSD: cathepsin D
  • CTSF: cathepsin F
  • CYP1B1: cytochrome P450, family 1, subfamily B, polypeptide 1
  • CYP2C9: cytochrome P450, family 2, subfamily C, polypeptide 9
  • DBT: dihydrolipoamide branched chain transacylase E2
  • DCN: decorin
  • DICER1: dicer 1, ribonuclease type III
  • DLD: dihydrolipoamide dehydrogenase
  • DPYD: dihydropyrimidine dehydrogenase
  • DPYS: dihydropyrimidinase
  • EGLN1: egl-9 family hypoxia-inducible factor 1
  • ELANE: elastase, neutrophil expressed
  • ENPP1: ectonucleotide pyrophosphatase/phosphodiesterase 1
  • EPM2A: epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
  • ERAP1: endoplasmic reticulum aminopeptidase 1
  • ERCC8: excision repair cross-complementation group 8
  • ETFA: electron-transfer-flavoprotein, alpha polypeptide
  • ETFDH: electron-transferring-flavoprotein dehydrogenase
  • ETHE1: ethylmalonic encephalopathy 1
  • EXOSC3: exosome component 3
  • FAH: fumarylacetoacetate hydrolase (fumarylacetoacetase)
  • FAM134B: family with sequence similarity 134, member B
  • FANCC: Fanconi anemia, complementation group C
  • FGF23: fibroblast growth factor 23
  • FLCN: folliculin
  • FLNA: filamin A, alpha
  • FOXL2: forkhead box L2
  • FTCD: formimidoyltransferase cyclodeaminase
  • FUCA1: fucosidase, alpha-L- 1, tissue
  • GAA: glucosidase, alpha; acid
  • GALC: galactosylceramidase
  • GALE: UDP-galactose-4-epimerase
  • GALK1: galactokinase 1
  • GALNS: galactosamine (N-acetyl)-6-sulfatase
  • GALT: galactose-1-phosphate uridylyltransferase
  • GBA: glucosidase, beta, acid
  • GCDH: glutaryl-CoA dehydrogenase
  • GLA: galactosidase, alpha
  • GLB1: galactosidase, beta 1
  • GLDC: glycine dehydrogenase (decarboxylating)
  • GNS: glucosamine (N-acetyl)-6-sulfatase
  • GPC3: glypican 3
  • GPI: glucose-6-phosphate isomerase
  • 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
  • HAMP: hepcidin antimicrobial peptide
  • HAX1: HCLS1 associated protein X-1
  • HBA2: hemoglobin, alpha 2
  • HBB: hemoglobin, beta
  • HEXA: hexosaminidase A (alpha polypeptide)
  • HEXB: hexosaminidase B (beta polypeptide)
  • HFE: hemochromatosis
  • HGD: homogentisate 1,2-dioxygenase
  • HGSNAT: heparan-alpha-glucosaminide N-acetyltransferase
  • HINT1: histidine triad nucleotide binding protein 1
  • HMGCL: 3-hydroxymethyl-3-methylglutaryl-CoA lyase
  • HPD: 4-hydroxyphenylpyruvate dioxygenase
  • HPRT1: hypoxanthine phosphoribosyltransferase 1
  • HPSE2: heparanase 2 (inactive)
  • HSD17B10: hydroxysteroid (17-beta) dehydrogenase 10
  • HSD17B4: hydroxysteroid (17-beta) dehydrogenase 4
  • IDS: iduronate 2-sulfatase
  • IDUA: iduronidase, alpha-L-
  • INS: insulin
  • INSR: insulin receptor
  • ITGB4: integrin, beta 4
  • ITPKC: inositol-trisphosphate 3-kinase C
  • IVD: isovaleryl-CoA dehydrogenase
  • KCNE2: potassium channel, voltage gated subfamily E regulatory beta subunit 2
  • KRT6A: keratin 6A, type II
  • LDHA: lactate dehydrogenase A
  • LDLR: low density lipoprotein receptor
  • LIPH: lipase, member H
  • LPIN2: lipin 2
  • LPL: lipoprotein lipase
  • LRP5: low density lipoprotein receptor-related protein 5
  • LRRK2: leucine-rich repeat kinase 2
  • MAP2K1: mitogen-activated protein kinase kinase 1
  • MAPT: microtubule-associated protein tau
  • MCCC1: methylcrotonoyl-CoA carboxylase 1 (alpha)
  • MCCC2: methylcrotonoyl-CoA carboxylase 2 (beta)
  • MCEE: methylmalonyl CoA epimerase
  • MLYCD: malonyl-CoA decarboxylase
  • MMAA: methylmalonic aciduria (cobalamin deficiency) cblA type
  • MMP14: matrix metallopeptidase 14 (membrane-inserted)
  • MMP2: matrix metallopeptidase 2
  • MMP20: matrix metallopeptidase 20
  • MSTN: myostatin
  • MTMR2: myotubularin related protein 2
  • MTRR: 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
  • MUT: methylmalonyl CoA mutase
  • MUTYH: mutY DNA glycosylase
  • MYH11: myosin, heavy chain 11, smooth muscle
  • NAGA: N-acetylgalactosaminidase, alpha-
  • NAGLU: N-acetylglucosaminidase, alpha
  • NEU1: sialidase 1 (lysosomal sialidase)
  • NHLRC1: NHL repeat containing E3 ubiquitin protein ligase 1
  • NPC1: Niemann-Pick disease, type C1
  • OAT: ornithine aminotransferase
  • OTC: ornithine carbamoyltransferase
  • OXCT1: 3-oxoacid CoA transferase 1
  • PAH: phenylalanine hydroxylase
  • PARK2: parkin RBR E3 ubiquitin protein ligase
  • PARK7: parkinson protein 7
  • 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
  • PFKM: phosphofructokinase, muscle
  • 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
  • PIK3CA: phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
  • PINK1: PTEN induced putative kinase 1
  • PKD1: polycystic kidney disease 1 (autosomal dominant)
  • PKLR: pyruvate kinase, liver and RBC
  • PML: promyelocytic leukemia
  • PNP: purine nucleoside phosphorylase
  • PNPLA2: patatin-like phospholipase domain containing 2
  • PNPO: pyridoxamine 5'-phosphate oxidase
  • POLR3A: polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
  • PPT1: palmitoyl-protein thioesterase 1
  • PRICKLE1: prickle homolog 1
  • PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
  • PRODH: proline dehydrogenase (oxidase) 1
  • PSMB8: proteasome subunit beta 8
  • PTEN: phosphatase and tensin homolog
  • PTPN22: protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
  • PYGL: phosphorylase, glycogen, liver
  • PYGM: phosphorylase, glycogen, muscle
  • QDPR: quinoid dihydropteridine reductase
  • RAB23: RAB23, member RAS oncogene family
  • RAB7A: RAB7A, member RAS oncogene family
  • RB1: retinoblastoma 1
  • RBM8A: RNA binding motif protein 8A
  • RNASEH2A: ribonuclease H2, subunit A
  • RNASEH2B: ribonuclease H2, subunit B
  • RNASEH2C: ribonuclease H2, subunit C
  • 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
  • SAMHD1: SAM domain and HD domain 1
  • SGSH: N-sulfoglucosamine sulfohydrolase
  • SLC1A3: solute carrier family 1 (glial high affinity glutamate transporter), member 3
  • SLC37A4: solute carrier family 37 (glucose-6-phosphate transporter), member 4
  • SMAD3: SMAD family member 3
  • SMAD4: SMAD family member 4
  • SNCA: synuclein, alpha (non A4 component of amyloid precursor)
  • SQSTM1: sequestosome 1
  • TAF1: TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
  • TAT: tyrosine aminotransferase
  • TET2: tet methylcytosine dioxygenase 2
  • TGFB1: transforming growth factor, beta 1
  • TOR1A: torsin family 1, member A (torsin A)
  • TPI1: triosephosphate isomerase 1
  • TPP1: tripeptidyl peptidase I
  • TREX1: three prime repair exonuclease 1
  • TWIST1: twist family bHLH transcription factor 1
  • TYMP: thymidine phosphorylase
  • UBA1: ubiquitin-like modifier activating enzyme 1
  • UBE3A: ubiquitin protein ligase E3A
  • UCHL1: ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
  • UGT1A1: UDP glucuronosyltransferase 1 family, polypeptide A1
  • UPB1: ureidopropionase, beta
  • USP9Y: ubiquitin specific peptidase 9, Y-linked
  • VCAN: versican
  • VCP: valosin containing protein
  • WFS1: Wolfram syndrome 1 (wolframin)

Source: Gene Ontology ConsortiumThis link leads to a site outside Genetics Home Reference..

 
Published: September 1, 2015