abnormal fatty acid oxidation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process of removal of one or more electrons from a fatty acid, with or without the concomitant removal of a proton or protons, by reaction with an electron-accepting substance, by addition of oxygen or by removal of hydrogen. (Mammalian Phenotype Ontology, MP_0010953)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010953
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16 gene mutations causing the abnormal fatty acid oxidation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACACB acetyl-CoA carboxylase beta
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain
ACOT11 acyl-CoA thioesterase 11
AKT1 v-akt murine thymoma viral oncogene homolog 1
C5AR2 complement component 5a receptor 2
CEACAM1 carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein)
CERS6 ceramide synthase 6
HADH hydroxyacyl-CoA dehydrogenase
LCLAT1 lysocardiolipin acyltransferase 1
MFSD2A major facilitator superfamily domain containing 2A
OMA1 OMA1 zinc metallopeptidase
PANK1 pantothenate kinase 1
PLIN5 perilipin 5
PPARA peroxisome proliferator-activated receptor alpha
RGS16 regulator of G-protein signaling 16
TBC1D1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1