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Basic information of TNFSF13B :

Official Symbol of Gene TNFSF13B
Species Homo sapiens
Entrez Gene ID 10673
Official Full Name TNF superfamily member 13b
Also known as DTL; BAFF; BLYS; CD257; TALL1; THANK; ZTNF4; TALL-1; TNLG7A; TNFSF20
Gene Type protein coding
dbXrefs Ensembl:ENSG00000102524 MIM:603969; AllianceGenome:HGNC:11929
Map Location 13q33.3

Sample information of multiple sclerosis:

Detected Sample Peripheral blood
Sample Detail white blood cells
Detected Method TaqMan assay
Disease giant cell arteritis (GCA) and systemic sclerosis (SSc)
Disease subtype N/A
Population European
Sample Size 1,728 biopsy-proven GCA patients from 4 European cohorts, 4,584 SSc patients from 3 European cohorts and 5,160 ethnically-matched healthy controls

Literature information of multiple sclerosis :

Pubmed ID 30586461
Year 2018
Title A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility

Results of multiple sclerosis :

Expression up-regulation
Risk type Disease risk
Result Our data suggest that the TNFSF13B functional variant does not contribute to the genetic network underlying GCA and SSc
Mechanism/Pathway The TNFSF13B (TNF superfamily member 13b) gene encodes BAFF, a cytokine with a crucial role in the differentiation and activation of B cells