increased white adipose tissue amount Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased quantity of fat-storing cells/tissue (Mammalian Phenotype Ontology, MP_0000008)
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38 gene mutations causing the increased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOR1 adiponectin receptor 1
ALMS1 Alstrom syndrome protein 1
ANKRD26 ankyrin repeat domain 26
APOC3 apolipoprotein C-III
BBS4 Bardet-Biedl syndrome 4
BRS3 bombesin-like receptor 3
CES1 carboxylesterase 1
CRTC1 CREB regulated transcription coactivator 1
CSHL1 chorionic somatomammotropin hormone-like 1
ESR1 estrogen receptor 1
FEN1 flap structure-specific endonuclease 1
FFAR4 free fatty acid receptor 4
FGF21 fibroblast growth factor 21
FGL1 fibrinogen-like 1
GDF15 growth differentiation factor 15
GHR growth hormone receptor
GNAS GNAS complex locus
GPRC6A G protein-coupled receptor, class C, group 6, member A
HDC histidine decarboxylase
HRH1 histamine receptor H1
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
IL18 interleukin 18
KDM3A lysine (K)-specific demethylase 3A
LEP leptin
NCOR2 nuclear receptor corepressor 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY6R neuropeptide Y receptor Y6 (pseudogene)
NTSR1 neurotensin receptor 1 (high affinity)
PCSK1 proprotein convertase subtilisin/kexin type 1
PNPLA2 patatin-like phospholipase domain containing 2
PPARG peroxisome proliferator-activated receptor gamma
PRLH prolactin releasing hormone
PYY peptide YY
RAI1 retinoic acid induced 1
SIM1 single-minded family bHLH transcription factor 1
TBC1D1 TBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1
TERF2IP telomeric repeat binding factor 2, interacting protein
WRN Werner syndrome, RecQ helicase-like