Home Details
| Official Symbol of Gene | F8 |
| Species | Homo sapiens |
| Entrez Gene ID | 2157 |
| Official Full Name | coagulation factor VIII |
| Also known as | AHF; F8B; F8C; HEMA; FVIII; THPH13; DXS1253E |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000185010 MIM:300841; AllianceGenome:HGNC:3546 |
| Map Location | Xq28 |
| Variation Type | SNP |
| refSNP ID | rs369414658 |
| Detected Sample | N/A |
| Sample Detail | X chromosome |
| Detected Method | Diseases 10th Revision (World Health O, 2004) code G38 ,PLINK |
| Disease | MS |
| Disease subtype | N/A |
| Population | UK |
| Sample Size | Genomic data for the X chromosome was obtained from the UK Biobank data field 22,421. |
| Pubmed ID | 35905688 |
| Year | 2022 |
| Title | X-linked genetic risk factors that promote autoimmunity and dampen remyelination are associated with multiple sclerosis susceptibility |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | concurrent disruption of both myelination and immune systems significantly increases the risk of MS onset in women |
| Mechanism/Pathway | immunity |

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