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Basic information of F8 :

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

Sample information of multiple sclerosis:

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.

Literature information of multiple sclerosis :

Pubmed ID 35905688
Year 2022
Title X-linked genetic risk factors that promote autoimmunity and dampen remyelination are associated with multiple sclerosis susceptibility

Results of multiple sclerosis :

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