Home Details
| Official Symbol of Gene | SLC25A36 |
| Species | Homo sapiens |
| Entrez Gene ID | 55186 |
| Official Full Name | solute carrier family 25 member 36 |
| Also known as | HHF8; PNC2 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000114120 MIM:616149; AllianceGenome:HGNC:25554 |
| Map Location | 3q23 |
| Variation Type | SNP |
| refSNP ID | rs908821 |
| 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, 2940 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 (1.12–1.46)), supporting a role for this proteoglycan in MS predisposition |
| Mechanism/Pathway | MS predisposition |

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