abnormal eating behavior Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal eating habit with excessive or insufficient consumption of food or any other abnormal pattern of food consumption. (Human Phenotype Ontology, HP_0100738)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100738
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Genes

22 genes associated with the abnormal eating behavior 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
BDNF brain-derived neurotrophic factor
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GRN granulin
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
LEP leptin
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
PRDM16 PR domain containing 16
PREPL prolyl endopeptidase-like
PSEN1 presenilin 1
SIM1 single-minded family bHLH transcription factor 1
SKI SKI proto-oncogene
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SNRPN small nuclear ribonucleoprotein polypeptide N