increased basal metabolism Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state (Mammalian Phenotype Ontology, MP_0008965)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008965
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Genes

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

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ARRDC3 arrestin domain containing 3
BRD2 bromodomain containing 2
DLL1 delta-like 1 (Drosophila)
FTO fat mass and obesity associated
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
KCNA3 potassium channel, voltage gated shaker related subfamily A, member 3
MARK2 MAP/microtubule affinity-regulating kinase 2
NCOR1 nuclear receptor corepressor 1
PTPN1 protein tyrosine phosphatase, non-receptor type 1
SSFA2 sperm specific antigen 2
TBC1D1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1
TGFB1 transforming growth factor, beta 1
VGF VGF nerve growth factor inducible