Detail Information of Genetic Polymorphisms
General Information of Drug Transporter (DT) | |||||
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DT ID | DTD0051 Transporter Info | ||||
Gene Name | ABCB5 | ||||
Protein Name | ATP-binding cassette sub-family B member 5 | ||||
Gene ID | |||||
UniProt ID | |||||
Genetic Polymorphisms of DT (GPD) | |||||
Genetic Polymorphism | rs17143212 | ||||
Site of GPD | chr7:20643261 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | C>T | ||||
Minor Allele Frequency | T=0.0705/353 (Global) | ||||
Genotype CT | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Haloperidol | Drug Info | Psychotic Disorders | Correlated with the increased drug toxicity in patients (compare with genotype CC) | [ 1] | |
Haloperidol | N.A. | Drug Toxicity | Genotype CT is associated with increased Drug Toxicity when treated with haloperidol in people with Psychotic Disorders as compared to genotype CC. | [ 1] | |
Haloperidol | N.A. | Psychotic Disorder | Genotype CT is associated with increased Drug Toxicity when treated with haloperidol in people with Psychotic Disorders as compared to genotype CC. | [ 1] | |
Allele T | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Talinolol | N.A. | Hypertriglyceridemia | Allele T is not associated with clearance of talinolol in healthy individuals as compared to allele C. | [ 2] | |
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Haloperidol | N.A. | Psychotic Disorder | Patients with the CC genotype and psychotic illnesses may be at a lower risk for haloperidol-induced toxicities as compared to patients with the CT genotype. Other genetic and clinical factors may also influence haloperidol-induced toxicities. | [ 1] | |
Genotype TT | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Haloperidol | N.A. | Psychotic Disorder | No patients with the TT genotype were present, but patients with the CT genotype and psychotic illnesses may be at a greater risk for haloperidol-induced toxicities as compared to patients with the CC genotype. Other genetic and clinical factors may also influence haloperidol-induced toxicities. | [ 1] | |
Genetic Polymorphism | rs10950831 | ||||
Site of GPD | chr7:20724751 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>C / G>T | ||||
Minor Allele Frequency | G=0.4520/894 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Cisplatin | N.A. | Ototoxicity | Allele G is not associated with risk of Ototoxicity when treated with cisplatin in people with Neoplasms as compared to allele T. | [ 3] | |
References | |||||
1 | The role of Abcb5 alleles in susceptibility to haloperidol-induced toxicity in mice and humans. PLoS Med. 2015 Feb 3;12(2):e1001782. | ||||
2 | Low heritability in pharmacokinetics of talinolol: a pharmacogenetic twin study on the heritability of the pharmacokinetics of talinolol, a putative probe drug of MDR1 and other membrane transporters. Genome Med. 2016 Nov 08;8(1):119. | ||||
3 | Promoter region variation in NFE2L2 influences susceptibility to ototoxicity in patients exposed to high cumulative doses of cisplatin. Pharmacogenomics J. 2017 Dec;17(6):515-520. |
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