absent subcutaneous adipose tissue Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of adipose tissue beneath the skin (Mammalian Phenotype Ontology, MP_0008843)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008843
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Genes

19 gene mutations causing the absent subcutaneous adipose tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ARHGAP1 Rho GTPase activating protein 1
CAV1 caveolin 1, caveolae protein, 22kDa
CHD2 chromodomain helicase DNA binding protein 2
EWSR1 EWS RNA-binding protein 1
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
HNF1A HNF1 homeobox A
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
LEF1 lymphoid enhancer-binding factor 1
LIPA lipase A, lysosomal acid, cholesterol esterase
LMNA lamin A/C
MCOLN1 mucolipin 1
POU3F2 POU class 3 homeobox 2
PPARG peroxisome proliferator-activated receptor gamma
SMTN smoothelin
TK2 thymidine kinase 2, mitochondrial
TWIST2 twist family bHLH transcription factor 2
ZFP36 ZFP36 ring finger protein
ZMPSTE24 zinc metallopeptidase STE24