Home Details
| Official Symbol of Gene | SH3GL2 |
| Species | Homo sapiens |
| Entrez Gene ID | 6456 |
| Official Full Name | SH3 domain containing GRB2 like 2, endophilin A1 |
| Also known as | CNSA2; SH3P4; EEN-B1; SH3D2A |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000107295 MIM:604465; AllianceGenome:HGNC:10831 |
| Map Location | 9p22.2 |
| Variation Type | SNP |
| refSNP ID | rs1755289 |
| Detected Sample | peripheral blood |
| Sample Detail | N/A |
| Detected Method | iPLEX Sequenom MassARRAY ,PicoGreen |
| Disease | MS |
| Disease subtype | N/A |
| Population | spanish |
| Sample Size | 2863 MS patients, 2935 healthy controls |
| Pubmed ID | 20944657 |
| Year | 2011 |
| Title | Replication of top markers of a genome-wide association study in multiple sclerosis in Spain |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Only rs9523762 mapping in the GPC5gene was significantly associated(G allele, P1.6 10 5 ; odds ratio (95% confidence interval)1.23 (1.12–1.41)), supporting a role for this proteoglycan in MS predisposition |
| Mechanism/Pathway | MS predisposition |

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