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| Official Symbol of Gene | ABCG2 |
| Species | Homo sapiens |
| Entrez Gene ID | 9429 |
| Official Full Name | ATP binding cassette subfamily G member 2 (Junior blood group) |
| Also known as | MRX; MXR; ABCP; BCRP; BMDP; MXR1; ABC15; BCRP1; CD338; GOUT1; MXR-1; CDw338; CDw388; UAQTL1; EST157481 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000118777 MIM:603756; AllianceGenome:HGNC:74 |
| Map Location | 4q22.1 |
| Detected Sample | Blood |
| Sample Detail | peripheral blood mononuclear cells |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | Germany |
| Sample Size | 832 multiple sclerosis patients from three sites in Germany (Go¨ttingen, n = 166; Rostock, n = 423, Berg, n = 194) |
| Pubmed ID | 19605531 |
| Year | 2009 |
| Title | ABC-transporter gene-polymorphisms are potential pharmacogenetic markers for mitoxantrone response in multiple sclerosis |
| Expression | up-regulation |
| Risk type | disease risk |
| Result | In conclusion, SNPs in ABC-transporter genes may serve as pharmacogenetic markers associated with clinical response to MX therapy in multiple sclerosis. |
| Mechanism/Pathway | ATP-binding cassette-transporters ABCB1 and ABCG2 represent multi-drug resistance mechanisms involved in active cellular MX efflux. |

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