Home Details
| Official Symbol of Gene | GTF2I |
| Species | Homo sapiens |
| Entrez Gene ID | 2969 |
| Official Full Name | general transcription factor Iii |
| Also known as | WBS; DIWS; SPIN; IB291; BAP135; BTKAP1; TFII-I; WBSCR6; GTFII-I |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000263001 MIM:601679; AllianceGenome:HGNC:4659 |
| Map Location | 7q11.23 |
| Variation Type | SNP |
| refSNP ID | rs117026326 |
| Detected Sample | Blood |
| Sample Detail | N/A |
| Detected Method | PCR,TaqMan |
| Disease | MS |
| Disease subtype | N/A |
| Population | northern Han Chinese |
| Sample Size | 168 patients with MS,168 controls |
| Pubmed ID | 31520790 |
| Year | 2019 |
| Title | The GTF2I rs117026326 polymorphism is associated with neuromyelitis optica spectrum disorder but not with multiple sclerosis in a Northern Han Chinese population |
| Risk Type | N/A |
| Main Result | negative |
| Result | The rs117026326 variant does not affect the risk for MS. |
| Mechanism/Pathway | N/A |

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