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 | BF; FB; BFD; GBG; CFAB; CFBD; PBF2; AHUS4; FBI12; H2-Bf; ARMD14 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000243649 MIM:138470; AllianceGenome:HGNC:1037 |
| Map Location | 6p21.33 |
| Variation Type | allele |
| refSNP ID | N/A |
Sample information of multiple sclerosis:
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | N/A |
Literature information of multiple sclerosis :
| Pubmed ID | 6120306 |
| Year | 1982 |
| Title | Factor B alleles and multiple sclerosis |
Results of multiple sclerosis :
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | We found a significantly lower frequency of the Bf F allele of the polymorphic factor B system in patients with definite multiple sclerosis (MS) but a normal frequency in patients with optic neuritis or suspected MS. |
| Mechanism/Pathway | N/A |
