abnormal white fat cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the number of fat cells with light coloration and few mitochondria (Mammalian Phenotype Ontology, MP_0009129)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009129
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14 gene mutations causing the abnormal white fat cell number 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
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CSPG4 chondroitin sulfate proteoglycan 4
ESR1 estrogen receptor 1
FGL1 fibrinogen-like 1
KSR1 kinase suppressor of ras 1
LEP leptin
NCOR2 nuclear receptor corepressor 2
PCNA proliferating cell nuclear antigen
PHF2 PHD finger protein 2
PPARG peroxisome proliferator-activated receptor gamma