abnormality of fatty-acid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of fatty acid metabolism. (Human Phenotype Ontology, HP_0004359)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004359
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Genes

21 genes associated with the abnormality of fatty-acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
ACAD8 acyl-CoA dehydrogenase family, member 8
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
ACADVL acyl-CoA dehydrogenase, very long chain
CPT2 carnitine palmitoyltransferase 2
CTNS cystinosin, lysosomal cystine transporter
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
PEX1 peroxisomal biogenesis factor 1
PEX12 peroxisomal biogenesis factor 12
PEX16 peroxisomal biogenesis factor 16
PEX19 peroxisomal biogenesis factor 19
PEX2 peroxisomal biogenesis factor 2
PEX5 peroxisomal biogenesis factor 5
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1