Home Details
| Official Symbol of Gene | ABCA7 |
| Species | Homo sapiens |
| Entrez Gene ID | 10347 |
| Official Full Name | ATP binding cassette subfamily A member 7 |
| Also known as | AD9; ABCX; ABCA-SSN |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000064687 MIM:605414; AllianceGenome:HGNC:37 |
| Map Location | 19p13.3 |
| Variation Type | polymorphisms |
| refSNP ID | ABCA7 4580(C, C/G, G) |
| Detected Sample | blood |
| Sample Detail | peripheral blood |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | n = 25 |
| Pubmed ID | 15593299 |
| Year | 2005 |
| Title | Homozygosity for the 168His variant of the minor histocompatibility antigen HA-1 is associated with reduced risk of primary Sjgren's syndrome |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | In cohorts of patients with systemic lupus erythematosus, rheumatoid arthritis and multiple sclerosis, no significant differences in the frequencies of ABCA7 and HA-1 allelic variants were observed relative to controls. |
| Mechanism/Pathway | N/A |

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