Basic information of KIF1B :
| Official Symbol of Gene | KIF1B |
| Species | Homo sapiens |
| Entrez Gene ID | 16636 |
| Official Full Name | kinesin family member 1B |
| Also known as | KLP; CMT2; CMT2A; CMT2A1; HMSNII; NBLST1 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000054523 MIM:605995; AllianceGenome:HGNC:16636 |
| Map Location | 1p36.22 |
| Variation Type | SNP |
| refSNP ID | rs3135388 |
Sample information of multiple sclerosis:
| Detected Sample | peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 326 MS cases |
Literature information of multiple sclerosis :
| Pubmed ID | 23528589 |
| Year | 2013 |
| Title | [The effect of genetic factors on the phenotypic expression of multiple sclerosis] |
Results of multiple sclerosis :
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | A more benign course and a higher frequency of an T allele of rs3135388 was found in familial cases compared to sporadic case |
| Mechanism/Pathway | the genetic basis of susceptibility |
