abnormal total fat pad weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in average total weight of the fat pad compared to controls (Mammalian Phenotype Ontology, MP_0020130)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0020130
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25 gene mutations causing the abnormal total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
AGR2 anterior gradient 2
ALOX5 arachidonate 5-lipoxygenase
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ATF4 activating transcription factor 4
CCL13 chemokine (C-C motif) ligand 13
EIF3M eukaryotic translation initiation factor 3, subunit M
FOXP2 forkhead box P2
FSHR follicle stimulating hormone receptor
IL18 interleukin 18
JUND jun D proto-oncogene
LPL lipoprotein lipase
MECP2 methyl CpG binding protein 2
NPY neuropeptide Y
NPY2R neuropeptide Y receptor Y2
OCA2 oculocutaneous albinism II
PDE10A phosphodiesterase 10A
PLIN1 perilipin 1
PPARG peroxisome proliferator-activated receptor gamma
PRCP prolylcarboxypeptidase (angiotensinase C)
PROX1 prospero homeobox 1
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
RBL1 retinoblastoma-like 1
RDH16 retinol dehydrogenase 16 (all-trans)
SAT1 spermidine/spermine N1-acetyltransferase 1