polyphagia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A neurological anomaly with gross overeating associated with an abnormally strong desire or need to eat. (Human Phenotype Ontology, HP_0002591)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002591
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Genes

12 genes associated with the polyphagia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
GRN granulin
LEPR leptin receptor
MAGEL2 melanoma antigen family L2
MAPT microtubule-associated protein tau
MBD5 methyl-CpG binding domain protein 5
NDN necdin, melanoma antigen (MAGE) family member
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PSEN1 presenilin 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SNRPN small nuclear ribonucleoprotein polypeptide N