abnormal white adipose tissue physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly in the connective tissue consisting of fat-storing cells and arranged in lobular groups or along minor blood vessels (Mammalian Phenotype Ontology, MP_0005670)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005670
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14 gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AQP7 aquaporin 7
CRTC3 CREB regulated transcription coactivator 3
DBI diazepam binding inhibitor (GABA receptor modulator, acyl-CoA binding protein)
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1
G0S2 G0/G1 switch 2
LGALS12 lectin, galactoside-binding, soluble, 12
LIPE lipase, hormone-sensitive
LPIN1 lipin 1
NCOR2 nuclear receptor corepressor 2
NR2C2 nuclear receptor subfamily 2, group C, member 2
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
PPARG peroxisome proliferator-activated receptor gamma
SAT1 spermidine/spermine N1-acetyltransferase 1
SORBS1 sorbin and SH3 domain containing 1