decreased white fat cell size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the size of fat cells with light coloration and few mitochondria (Mammalian Phenotype Ontology, MP_0009133)
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31 gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AGTR2 angiotensin II receptor, type 2
ARRDC3 arrestin domain containing 3
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CNOT3 CCR4-NOT transcription complex, subunit 3
CRTC3 CREB regulated transcription coactivator 3
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
ESRRA estrogen-related receptor alpha
FGF21 fibroblast growth factor 21
FTO fat mass and obesity associated
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
LGALS12 lectin, galactoside-binding, soluble, 12
MFSD2A major facilitator superfamily domain containing 2A
MIR378A microRNA 378a
NCOA3 nuclear receptor coactivator 3
NCOR1 nuclear receptor corepressor 1
NCOR2 nuclear receptor corepressor 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NR1H4 nuclear receptor subfamily 1, group H, member 4
NR2C2 nuclear receptor subfamily 2, group C, member 2
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
PHF2 PHD finger protein 2
PLIN1 perilipin 1
PPARG peroxisome proliferator-activated receptor gamma
RAPGEF3 Rap guanine nucleotide exchange factor (GEF) 3
RBL1 retinoblastoma-like 1
SAMD4A sterile alpha motif domain containing 4A
SERTAD2 SERTA domain containing 2
SRA1 steroid receptor RNA activator 1
TGFB1 transforming growth factor, beta 1
TRIB1 tribbles pseudokinase 1