schizophrenia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A major psychotic disorder characterized by abnormalities in the perception or expression of reality. It affects the cognitive and psychomotor functions. Common clinical signs and symptoms include delusions, hallucinations, disorganized thinking, and retreat from reality.|A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. (Experimental Factor Ontology, EFO_0000692)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100753
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Genes

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

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
DISC2 disrupted in schizophrenia 2 (non-protein coding)
SHANK3 SH3 and multiple ankyrin repeat domains 3
TBX1 T-box 1
WFS1 Wolfram syndrome 1 (wolframin)