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Basic information of CFB :

Official Symbol of Gene CFB
Species Homo sapiens
Entrez Gene ID 629
Official Full Name complement factor B
Also known as 6p21.33
Gene Type protein coding
dbXrefs Ensembl:ENSG00000243649 MIM:138470; AllianceGenome:HGNC:1037
Map Location 6p21.33
Variation Type Allele
refSNP ID NA

Sample information of multiple sclerosis:

Detected Sample peripheral blood
Sample Detail N/A
Detected Method PCR
Disease MS
Disease subtype NA
Population North-East England
Sample Size 101MS/270Health

Literature information of multiple sclerosis :

Pubmed ID 1797634
Year 1991
Title Factor B (BF) Allotypes and Multiple Sclerosis in North-East England

Results of multiple sclerosis :

Risk Type Phenotypic risk
Main Result Positive
Result There is a suggestion that the BF*S and Dw2+ alleles are more prevalent in chronic progressive patients, implying that in Dw2+ patients BF may influence the progression of the disease.
Mechanism/Pathway N/A