fatty acid catabolic process Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The chemical reactions and pathways resulting in the breakdown of a fatty acid, any of the aliphatic monocarboxylic acids that can be liberated by hydrolysis from naturally occurring fats and oils. Fatty acids are predominantly straight-chain acids of 4 to 24 carbon atoms, which may be saturated or unsaturated; branched fatty acids and hydroxy fatty acids also occur, and very long chain acids of over 30 carbons are found in waxes. (Gene Ontology, GO_0009062)
External Link http://amigo.geneontology.org/amigo/term/GO:0009062
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Genes

63 genes participating in the fatty acid catabolic process biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
ABCD2 ATP-binding cassette, sub-family D (ALD), member 2
ABCD3 ATP-binding cassette, sub-family D (ALD), member 3
ACAA1 acetyl-CoA acyltransferase 1
ACAD11 acyl-CoA dehydrogenase family, member 11
ACADL acyl-CoA dehydrogenase, long chain
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain
ACADVL acyl-CoA dehydrogenase, very long chain
ACOT7 acyl-CoA thioesterase 7
ACOT8 acyl-CoA thioesterase 8
ACOX1 acyl-CoA oxidase 1, palmitoyl
ACOX2 acyl-CoA oxidase 2, branched chain
ACOX3 acyl-CoA oxidase 3, pristanoyl
ACOXL acyl-CoA oxidase-like
ADIPOQ adiponectin, C1Q and collagen domain containing
AMACR alpha-methylacyl-CoA racemase
BDH2 3-hydroxybutyrate dehydrogenase, type 2
CPT1A carnitine palmitoyltransferase 1A (liver)
CPT1B carnitine palmitoyltransferase 1B (muscle)
CPT1C carnitine palmitoyltransferase 1C
CPT2 carnitine palmitoyltransferase 2
CRAT carnitine O-acetyltransferase
CROT carnitine O-octanoyltransferase
CYP4A11 cytochrome P450, family 4, subfamily A, polypeptide 11
CYP4F12 cytochrome P450, family 4, subfamily F, polypeptide 12
CYP4F2 cytochrome P450, family 4, subfamily F, polypeptide 2
CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial
ECH1 enoyl CoA hydratase 1, peroxisomal
ECHS1 enoyl CoA hydratase, short chain, 1, mitochondrial
ECI1 enoyl-CoA delta isomerase 1
EHHADH enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
ETFDH electron-transferring-flavoprotein dehydrogenase
FAAH fatty acid amide hydrolase
HACL1 2-hydroxyacyl-CoA lyase 1
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
HAO1 hydroxyacid oxidase (glycolate oxidase) 1
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
IRG1 immunoresponsive 1 homolog (mouse)
LEP leptin
LIPE lipase, hormone-sensitive
LPIN1 lipin 1
LPIN2 lipin 2
LPIN3 lipin 3
MCEE methylmalonyl CoA epimerase
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MUT methylmalonyl CoA mutase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PEX13 peroxisomal biogenesis factor 13
PEX2 peroxisomal biogenesis factor 2
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase
PLA2G15 phospholipase A2, group XV
PPARD peroxisome proliferator-activated receptor delta
SCP2 sterol carrier protein 2
SESN2 sestrin 2
SLC25A17 solute carrier family 25 (mitochondrial carrier; peroxisomal membrane protein, 34kDa), member 17
SLC27A2 solute carrier family 27 (fatty acid transporter), member 2
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4