Home Details
| Official Symbol of Gene | IGF1 |
| Species | Homo sapiens |
| Entrez Gene ID | 3479 |
| Official Full Name | insulin like growth factor 1 |
| Also known as | IGF; MGF; IGFI; IGF-I |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000017427 MIM:147440; AllianceGenome:HGNC:5464 |
| Map Location | 12q23.2 |
| Detected Sample | brain |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 339cases/431controls |
| Pubmed ID | 28427698 |
| Year | 2017 |
| Title | Novel functional polymorphism in IGF-1 gene associated with multiple sclerosis: A new insight to MS |
| Expression | up-regulation |
| Risk type | Disease risk |
| Result | According to IGF-1 roles in CNS and our results, this study suggests that low IGF-1 level may be associated with susceptibility to MS |
| Mechanism/Pathway | identified a T to C single nucleotide substitution at position 1089 and a C to T at position 383 from transcription start site in the IGF-1 gene promoter. |

2023,CopyRight © HMU. College of Bioinformatics Science and Technology, Harbin, China.