Home Details
| Official Symbol of Gene | NR3C1 |
| Species | Homo sapiens |
| Entrez Gene ID | 2908 |
| Official Full Name | nuclear receptor subfamily 3 group C member 1 |
| Also known as | GR; GCR; GRL; GCCR; GCRST |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000113580 MIM:138040; AllianceGenome:HGNC:7978 |
| Map Location | 5q31.3 |
| Variation Type | polymorphisms |
| refSNP ID | rs6196(CC) |
| Detected Sample | blood |
| Sample Detail | peripheral blood lymphocytes |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | CIS, RRMS, SPMS |
| Population | Caucasian Greek |
| Sample Size | Sixty Caucasian Greek patients |
| Pubmed ID | 27000245 |
| Year | 2016 |
| Title | Sequencing analysis of the human glucocorticoid receptor (NR3C1) gene in multiple sclerosis patients |
| Risk Type | Phenotypic risk |
| Main Result | Negative |
| Result | None of the identified alleles/genotypes were found to be associated with the severity of disease, response to glucocorticoids and disease subtypes. |
| Mechanism/Pathway | N/A |

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