decreased abdominal fat pad weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than average weight of the encapsulated adipose tissue in the abdomen (Mammalian Phenotype Ontology, MP_0009287)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009287
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Genes

9 gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
DUSP1 dual specificity phosphatase 1
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KLF3 Kruppel-like factor 3 (basic)
NPC1 Niemann-Pick disease, type C1
NR2C2 nuclear receptor subfamily 2, group C, member 2
PPARD peroxisome proliferator-activated receptor delta
PRLR prolactin receptor
TRPV1 transient receptor potential cation channel, subfamily V, member 1