abnormal mesenteric fat pad morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the encapsulated adipose tissue associated with the mesentery (Mammalian Phenotype Ontology, MP_0008903)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008903
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Genes

16 gene mutations causing the abnormal mesenteric fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CIDEC cell death-inducing DFFA-like effector c
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
DHCR24 24-dehydrocholesterol reductase
GDF15 growth differentiation factor 15
IL1R1 interleukin 1 receptor, type I
LEPR leptin receptor
NPY6R neuropeptide Y receptor Y6 (pseudogene)
OMA1 OMA1 zinc metallopeptidase
PHF2 PHD finger protein 2
PPARD peroxisome proliferator-activated receptor delta
PRCP prolylcarboxypeptidase (angiotensinase C)
RLN3 relaxin 3
SIK3 SIK family kinase 3
SLC30A5 solute carrier family 30 (zinc transporter), member 5