Home Details
| Official Symbol of Gene | CBLB |
| Species | Homo sapiens |
| Entrez Gene ID | 868 |
| Official Full Name | Cbl proto-oncogene B |
| Also known as | Cbl-b; RNF56; Nbla00127 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000114423 MIM:604491; AllianceGenome:HGNC:1542 |
| Map Location | 3q13.11 |
| Variation Type | SNP |
| refSNP ID | rs2028597 |
| Detected Sample | blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | RRMS |
| Population | N/A |
| Sample Size | N/A |
| Pubmed ID | 25261476 |
| Year | 2014 |
| Title | A multiple sclerosis-associated variant of CBLB links genetic risk with type I IFN function |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Interestingly, binding was predicted only for the C/EBPb binding site if it contained the risk (T) allele of rs12487066 , whereas the prediction for rs9657904 and rs2028597 showed no differential binding for C/EBPb. |
| Mechanism/Pathway | N/A |

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