Confusion Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Lack of clarity and coherence of thought, perception, understanding, or action. (Human Phenotype Ontology, HP_0001289)
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7 genes associated with the Confusion phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARRB2 arrestin, beta 2
COMT catechol-O-methyltransferase
DRD2 dopamine receptor D2
OPRM1 opioid receptor, mu 1
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced
UGT2B7 UDP glucuronosyltransferase 2 family, polypeptide B7