Detail Information of Genetic Polymorphisms
General Information of Drug Transporter (DT) | |||||
---|---|---|---|---|---|
DT ID | DTD0016 Transporter Info | ||||
Gene Name | ABCC5 | ||||
Protein Name | Multidrug resistance-associated protein 5 | ||||
Gene ID | |||||
UniProt ID | |||||
Genetic Polymorphisms of DT (GPD) | |||||
Genetic Polymorphism | rs10937158 | ||||
Site of GPD | chr3:183990651 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>C | ||||
Minor Allele Frequency | T=0.3171/1588 (Global) | ||||
Allele T | Click to Show/Hide the Full List of Affected Drugs: 9 Drugs in Total | ||||
Irinotecan | Drug Info | Colorectal Neoplasm | Correlated with the decreased diarrhea risk in patients (compare with genotype CC) | [ 1] | |
Fluorouracil | Drug Info | Colorectal Neoplasm | Correlated with the decreased diarrhea risk in patients (compare with genotype CC) | [ 1] | |
Leucovorin | Drug Info | Colorectal Neoplasm | Correlated with the decreased diarrhea risk in patients (compare with genotype CC) | [ 1] | |
Fluorouracil | N.A. | Diarrhea | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Irinotecan | N.A. | Diarrhea | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Leucovorin | N.A. | Diarrhea | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Fluorouracil | N.A. | Colorectal Neoplasms | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Allele T is associated with decreased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype CC. | [ 1] | |
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the CC genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the CT + TT genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the CC genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the CT + TT genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the CC genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the CT + TT genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genotype CT | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the CT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the CT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the CT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genotype TT | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the TT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the TT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the TT genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the CC genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genetic Polymorphism | rs3749438 | ||||
Site of GPD | chr3:183987396 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>A | ||||
Minor Allele Frequency | A=0.3339/1672 (Global) | ||||
Allele A | Click to Show/Hide the Full List of Affected Drugs: 9 Drugs in Total | ||||
Irinotecan | Drug Info | Colorectal Neoplasm | Correlated with the increased diarrhea risk in patients (compare with genotype GG) | [ 1] | |
Fluorouracil | Drug Info | Colorectal Neoplasm | Correlated with the increased diarrhea risk in patients (compare with genotype GG) | [ 1] | |
Leucovorin | Drug Info | Colorectal Neoplasm | Correlated with the increased diarrhea risk in patients (compare with genotype GG) | [ 1] | |
Fluorouracil | N.A. | Diarrhea | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Irinotecan | N.A. | Diarrhea | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Leucovorin | N.A. | Diarrhea | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Fluorouracil | N.A. | Colorectal Neoplasms | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Allele A is associated with increased risk of Diarrhea when treated with fluorouracil, irinotecan and leucovorin in people with Colorectal Neoplasms as compared to genotype GG. | [ 1] | |
Genotype AA | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the AA genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the AA genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the AA genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genotype AG | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the AG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the AG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the AG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have an increased risk for grade 3–4 severe diarrhea as compared to patients with the GG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genotype GG | Click to Show/Hide the Full List of Affected Drugs: 3 Drugs in Total | ||||
Fluorouracil | N.A. | Colorectal Neoplasms | Patients with the GG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the AA or AG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Irinotecan | N.A. | Colorectal Neoplasms | Patients with the GG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the AA or AG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Leucovorin | N.A. | Colorectal Neoplasms | Patients with the GG genotype and Colorectal Neoplasms who are treated with fluorouracil, irinotecan and leucovorin may have a decreased, but not absent, risk for grade 3–4 severe diarrhea as compared to patients with the AA or AG genotype. Other genetic and clinical factors may also influence a patient's risk for grade 3–4 severe diarrhea. | [ 1] | |
Genetic Polymorphism | rs939338 | ||||
Site of GPD | chr3:183986280 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>A / G>C / G>T | ||||
Minor Allele Frequency | G=0.3010/595 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 2 Drugs in Total | ||||
Cisplatin | N.A. | Progression-free Survival | Allele G is associated with decreased progression-free survival when treated with cisplatin and doxorubicin in people with Osteosarcoma as compared to allele A. | [ 2] | |
Doxorubicin | N.A. | Progression-free Survival | Allele G is associated with decreased progression-free survival when treated with cisplatin and doxorubicin in people with Osteosarcoma as compared to allele A. | [ 2] | |
Genotype AA | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Genetic Polymorphism | rs562 | ||||
Site of GPD | chr3:183920057 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>A / T>C / T>G | ||||
Minor Allele Frequency | T=0.4580/906 (Global) | ||||
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Irinotecan | N.A. | Drug Toxicity | Genotype CC is associated with increased likelihood of Drug Toxicity when treated with irinotecan in people with Colorectal Neoplasms as compared to genotypes CT + TT. | [ 4] | |
Allele T | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Drugs For Treatment Of Tuberculosis | N.A. | Toxic Liver Disease | Allele T is not associated with risk of Toxic liver disease due to Drugs For Treatment Of Tuberculosis in people with Tuberculosis as compared to allele C. | [ 5] | |
Genetic Polymorphism | rs1533682 | ||||
Site of GPD | chr3:183917091 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>A / T>C | ||||
Minor Allele Frequency | T=0.3000/593 (Global) | ||||
Genotype TT | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Doxorubicin | N.A. | Drug Toxicity | Genotype TT is associated with increased clearance of doxorubicin in women with Breast Neoplasms as compared to genotypes CC + CT. | [ 6] | |
Genetic Polymorphism | rs3749442 | ||||
Site of GPD | chr3:183942797 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>A | ||||
Minor Allele Frequency | G=0.7550/1494 (Global) | ||||
Allele A | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Glyburide | N.A. | Drug Toxicity | Allele A is associated with increased response to glibenclamide in people with as compared to allele G. | [ 7] | |
Genotype AA | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype AA is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AG + GG. | [ 3] | |
Genotypes AA + AG | Click to Show/Hide the Full List of Affected Drugs: 2 Drugs in Total | ||||
Cannabidiol | N.A. | Anemia | Genotypes AA + AG are associated with decreased response to cannabidiol in people with Epilepsy as compared to genotype GG. | [ 8] | |
Cannabidiol | N.A. | Sedation | Genotypes AA + AG are associated with increased likelihood of sedation when treated with cannabidiol in people with Epilepsy as compared to genotype GG. | [ 8] | |
Genetic Polymorphism | rs4148579 | ||||
Site of GPD | chr3:183967461 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>A / T>C / T>G | ||||
Minor Allele Frequency | T=0.3000/593 (Global) | ||||
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes CT + TT. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes CT + TT. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes CT + TT. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes CT + TT. | [ 3] | |
Genetic Polymorphism | rs4148580 | ||||
Site of GPD | chr3:183967395 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>A / T>C | ||||
Minor Allele Frequency | T=0.8500/1682 (Global) | ||||
Genotype CC | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype CC is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma. | [ 3] | |
Genetic Polymorphism | rs4148575 | ||||
Site of GPD | chr3:183984487 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | A>G / A>T | ||||
Minor Allele Frequency | A=0.3210/635 (Global) | ||||
Genotype GG | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Genetic Polymorphism | rs1132776 | ||||
Site of GPD | chr3:183978614 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | A>C / A>G / A>T | ||||
Minor Allele Frequency | A=0.3240/641 (Global) | ||||
Genotype GG | Click to Show/Hide the Full List of Affected Drugs: 4 Drugs in Total | ||||
Antineoplastic And Immunomodulating Agents | N.A. | Neutropenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Leukopenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Thrombocytopenia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Antineoplastic And Immunomodulating Agents | N.A. | Anemia | Genotype GG is associated with increased severity of Neutropenia, Leukopenia, Thrombocytopenia or Anemia when treated with Antineoplastic And Immunomodulating Agents in children with Precursor Cell Lymphoblastic Leukemia-Lymphoma as compared to genotypes AA + AG. | [ 3] | |
Genetic Polymorphism | rs2293001 | ||||
Site of GPD | chr3:183982423 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | C>A / C>G / C>T | ||||
Minor Allele Frequency | C=0.5710/1130 (Global) | ||||
Allele T | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Drugs For Treatment Of Tuberculosis | N.A. | Toxic Liver Disease | Allele T is not associated with risk of Toxic liver disease due to Drugs For Treatment Of Tuberculosis in people with Tuberculosis as compared to allele C. | [ 5] | |
Allele C | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele C is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele T. | [ 9] | |
Genetic Polymorphism | rs9838667 | ||||
Site of GPD | chr3:183946890 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | T>C / T>G | ||||
Minor Allele Frequency | T=0.6570/1300 (Global) | ||||
Allele T | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Drugs For Treatment Of Tuberculosis | N.A. | Toxic Liver Disease | Allele T is not associated with risk of Toxic liver disease due to Drugs For Treatment Of Tuberculosis in people with Tuberculosis as compared to allele G. | [ 5] | |
Genetic Polymorphism | rs4148557 | ||||
Site of GPD | chr3:184015996 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | A>C / A>G / A>T | ||||
Minor Allele Frequency | A=0.3440/680 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele G is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele A. | [ 9] | |
Genetic Polymorphism | rs4148572 | ||||
Site of GPD | chr3:184002711 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | C>A / C>G | ||||
Minor Allele Frequency | C=0.8490/1680 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele G is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele C. | [ 9] | |
Genetic Polymorphism | rs3792581 | ||||
Site of GPD | chr3:183978082 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | C>A | ||||
Minor Allele Frequency | C=0.7530/1490 (Global) | ||||
Allele A | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele A is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele C. | [ 9] | |
Genetic Polymorphism | rs3805111 | ||||
Site of GPD | chr3:183972201 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>A / G>C | ||||
Minor Allele Frequency | G=0.9400/1860 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele G is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele A. | [ 9] | |
Genetic Polymorphism | rs2139560 | ||||
Site of GPD | chr3:183936081 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | A>C / A>G / A>T | ||||
Minor Allele Frequency | A=0.3020/597 (Global) | ||||
Allele A | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele A is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele G. | [ 9] | |
Genetic Polymorphism | rs8180093 | ||||
Site of GPD | chr3:183924515 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | G>A | ||||
Minor Allele Frequency | G=0.9210/1822 (Global) | ||||
Allele G | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele G is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele A. | [ 9] | |
Genetic Polymorphism | rs1000002 | ||||
Site of GPD | chr3:183917980 (GRCh38.p12) | ||||
GPD Type | SNP | ||||
Allele(s) in dbSNP | C>T | ||||
Minor Allele Frequency | C=0.6250/1236 (Global) | ||||
Allele T | Click to Show/Hide the Full List of Affected Drugs: 1 Drugs in Total | ||||
Antiepileptics | N.A. | Toxic Liver Disease | Allele T is not associated with resistance to antiepileptics in people with Epilepsy as compared to allele C. | [ 9] | |
References | |||||
1 | ABCC5 and ABCG1 polymorphisms predict irinotecan-induced severe toxicity in metastatic colorectal cancer patients. Pharmacogenet Genomics. 2015 Dec;25(12):573-83. | ||||
2 | A First Step toward Personalized Medicine in Osteosarcoma: Pharmacogenetics as Predictive Marker of Outcome after Chemotherapy-Based Treatment. Clin Cancer Res. 2015 Aug 01;21(15):3436-41. | ||||
3 | Association between genetic variants of membrane transporters and the risk of high-grade hematologic adverse events in a cohort of Mexican children with B-cell acute lymphoblastic leukemia. Front Oncol. 2023;13:1276352. | ||||
4 | Single nucleotide polymorphisms of ABCC5 and ABCG1 transporter genes correlate to irinotecan-associated gastrointestinal toxicity in colorectal cancer patients: a DMET microarray profiling study. Cancer Biol Ther. 2011 Nov 01;12(9):780-7. | ||||
5 | Association of ABCC Gene Polymorphism With Susceptibility to Antituberculosis Drug-Induced Hepatotoxicity in Western Han Patients With Tuberculosis. J Clin Pharmacol. 2020 Mar;60(3):361-368. | ||||
6 | Pharmacogenetics of ABCB5, ABCC5 and RLIP76 and doxorubicin pharmacokinetics in Asian breast cancer patients. Pharmacogenomics J. 2017 Jul;17(4):337-343. | ||||
7 | Genetic and Clinical Predictive Factors of Sulfonylurea Failure in Patients with Type 2 Diabetes. Diabetes Technol Ther. 2016 Sep;18(9):586-93. | ||||
8 | Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment-Resistant Epilepsy. Clin Pharmacol Ther. 2021 Nov;110(5):1368-1380. | ||||
9 | Gene-wide tagging study of the association between ABCC2, ABCC5 and ABCG2 genetic polymorphisms and multidrug resistance in epilepsy. Pharmacogenomics. 2011 Mar;12(3):319-25. |
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