Home Details
| Official Symbol of Gene | IFNG |
| Species | Homo sapiens |
| Entrez Gene ID | 3458 |
| Official Full Name | interferon gamma |
| Also known as | IFG; IFI; IMD69 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000111537 MIM:147570; AllianceGenome:HGNC:5438 |
| Map Location | 12q15 |
| Variation Type | allele |
| refSNP ID | I1(761)*CA12 |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | DNA sequencers |
| Disease | MS |
| Disease subtype | N/A |
| Population | USA, Northern Ireland and Belgium |
| Sample Size | 221 patients (64 men and 157 women),442 controls (128 men and 314 women) |
| Pubmed ID | 15674394 |
| Year | 2005 |
| Title | IFNG polymorphisms are associated with gender differences in susceptibility to multiple sclerosis |
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | Polymorphisms of IFNG may contribute to differences in susceptibility to MS between men and women |
| Mechanism/Pathway | Men carriers of I1(761)*CA13 , which is in strong linkage disequilibrium with the 30(325)*A, have increased susceptibilit |

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