withdrawal disorder Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol. (Human Disease Ontology, DOID_0060001)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0060001
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Genes

16 genes associated with the disease withdrawal disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
KDM4C lysine (K)-specific demethylase 4C 1.0013
KIAA1407 KIAA1407 0.945129
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2 0.926808
NIM1K NIM1 serine/threonine protein kinase 0.898875
AKAP6 A kinase (PRKA) anchor protein 6 0.821119
MTUS2 microtubule associated tumor suppressor candidate 2 0.807358
PSAP prosaposin 0.800979
RARB retinoic acid receptor, beta 0.783178
LUZP2 leucine zipper protein 2 0.770703
AADAT aminoadipate aminotransferase 0.76582
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 0.764371
ADRB2 adrenoceptor beta 2, surface 0.748359
GPR176 G protein-coupled receptor 176 0.746396
FGF12 fibroblast growth factor 12 0.74049
PPP6R1 protein phosphatase 6, regulatory subunit 1 0.687994
ADAMTS9 ADAM metallopeptidase with thrombospondin type 1 motif, 9 0.683601