Pruritus Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Pruritus is an itch or a sensation that makes a person want to scratch. This term refers to an abnormally increased disposition to experience pruritus. (Human Phenotype Ontology, HP_0000989)
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Genes

16 genes associated with the Pruritus phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
ARRB2 arrestin, beta 2
COL7A1 collagen, type VII, alpha 1
COMT catechol-O-methyltransferase
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
JAK2 Janus kinase 2
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MMP1 matrix metallopeptidase 1
OPRM1 opioid receptor, mu 1
STAT6 signal transducer and activator of transcription 6, interleukin-4 induced
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8
UGT2B7 UDP glucuronosyltransferase 2 family, polypeptide B7