abnormal retroperitoneal 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 found on the dorsal side of the peritoneum (Mammalian Phenotype Ontology, MP_0005337)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005337
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Genes

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

Symbol Name
ASIP agouti signaling protein
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CIDEC cell death-inducing DFFA-like effector c
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1
ESR1 estrogen receptor 1
ESRRA estrogen-related receptor alpha
GDF15 growth differentiation factor 15
GHR growth hormone receptor
GNG3 guanine nucleotide binding protein (G protein), gamma 3
GPAM glycerol-3-phosphate acyltransferase, mitochondrial
GPR12 G protein-coupled receptor 12
IL1R1 interleukin 1 receptor, type I
KDM3A lysine (K)-specific demethylase 3A
KLF3 Kruppel-like factor 3 (basic)
LIPA lipase A, lysosomal acid, cholesterol esterase
MSTN myostatin
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY1R neuropeptide Y receptor Y1
NPY5R neuropeptide Y receptor Y5
NPY6R neuropeptide Y receptor Y6 (pseudogene)
NR1H4 nuclear receptor subfamily 1, group H, member 4
PLIN1 perilipin 1
PLVAP plasmalemma vesicle associated protein
POMC proopiomelanocortin
PPARG peroxisome proliferator-activated receptor gamma
PRCP prolylcarboxypeptidase (angiotensinase C)
RCAN2 regulator of calcineurin 2
SLC27A5 solute carrier family 27 (fatty acid transporter), member 5
SLC30A5 solute carrier family 30 (zinc transporter), member 5
WRN Werner syndrome, RecQ helicase-like