Basic information of RGS7 :
| Official Symbol of Gene | RGS7 |
| Species | Homo sapiens |
| Entrez Gene ID | 6000 |
| Official Full Name | regulator of G protein signaling 7 |
| Also known as | NA |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000182901 MIM:602517; AllianceGenome:HGNC:10003 |
| Map Location | N/A |
| Variation Type | Allele |
| refSNP ID | NA |
Sample information of multiple sclerosis:
| Detected Sample | peripheral blood |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | NA |
| Population | NA |
| Sample Size | 405MS/ |
Literature information of multiple sclerosis :
| Pubmed ID | 19626040 |
| Year | 2009 |
| Title | Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis |
Results of multiple sclerosis :
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | In this follow-up study, we saturated the region with ~700 SNPs (average spacing of 10kb per SNP) in search of disease associated variation within this region. We found preliminary evidence to suggest that common variation within the RGS7 locus may be involved in disease susceptibility. |
| Mechanism/Pathway | Our own second-generation genome-wide linkage study identified a handful of non-MHC regions with suggestive linkage. |
