abnormal basal metabolism Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state (Mammalian Phenotype Ontology, MP_0008961)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008961
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Genes

31 gene mutations causing the abnormal basal metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACOT13 acyl-CoA thioesterase 13
AKT1 v-akt murine thymoma viral oncogene homolog 1
ARRDC3 arrestin domain containing 3
BRD2 bromodomain containing 2
CD36 CD36 molecule (thrombospondin receptor)
CLOCK clock circadian regulator
DLL1 delta-like 1 (Drosophila)
FTO fat mass and obesity associated
GDF15 growth differentiation factor 15
GDF3 growth differentiation factor 3
GFRA2 GDNF family receptor alpha 2
GNAS GNAS complex locus
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
HTR6 5-hydroxytryptamine (serotonin) receptor 6, G protein-coupled
IGFBP3 insulin-like growth factor binding protein 3
KCNA3 potassium channel, voltage gated shaker related subfamily A, member 3
MARK2 MAP/microtubule affinity-regulating kinase 2
NCOR1 nuclear receptor corepressor 1
OMA1 OMA1 zinc metallopeptidase
PER1 period circadian clock 1
PER2 period circadian clock 2
PTPN1 protein tyrosine phosphatase, non-receptor type 1
PTRF polymerase I and transcript release factor
SSFA2 sperm specific antigen 2
TBC1D1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1
TBC1D4 TBC1 domain family, member 4
TGFB1 transforming growth factor, beta 1
UMOD uromodulin
UQCRFS1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1
VGF VGF nerve growth factor inducible