Home Details
| Official Symbol of Gene | GFI1 |
| Species | Homo sapiens |
| Entrez Gene ID | 2672 |
| Official Full Name | growth factor independent 1 transcriptional repressor |
| Also known as | SCN2; GFI-1; GFI1A; ZNF163 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000162676 MIM:600871; AllianceGenome:HGNC:4237 |
| Map Location | 1p22.1 |
| Detected Sample | PBMC |
| Sample Detail | N/A |
| Detected Method | RT-PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | N/A |
| Pubmed ID | 21602820 |
| Year | 2011 |
| Title | Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genes |
| Expression | up-regulation |
| Risk type | Disease risk |
| Result | The GFI1 promoter interacted with several regions of the intron, interaction that was stronger in the activated than in the control PBMCs.GFI1 is robustly upregulated in activated PBMCs. |
| Mechanism/Pathway | MS is a heterogeneous immunopathy likely caused by the joint participation of different peripheral blood cells in the central nervous system.Interestingly, malfunction of GFI1, which encodes a zinc-finger transcription factor, causes abnormal or malignant haematopoiesis, and therefore could play a role in an autoimmune disease such as MS. |

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