Basic information of SLC9A9 :
| Official Symbol of Gene | SLC9A9 |
| Species | Homo sapiens |
| Entrez Gene ID | 285195 |
| Official Full Name | solute carrier family 9 member A9 |
| Also known as | NHE9; AUTS16 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000181804 MIM:608396; AllianceGenome:HGNC:20653 |
| Map Location | 3q24 |
| Variation Type | SNP |
| refSNP ID | rs11919382 |
Sample information of multiple sclerosis:
| Detected Sample | brain |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | N/A |
Literature information of multiple sclerosis :
| Pubmed ID | 27766536 |
| Year | 2017 |
| Title | Genetic Variants and Multiple Sclerosis Risk Gene SLC9A9 Expression in Distinct Human Brain Regions |
Results of multiple sclerosis :
| Risk Type | Disease risk |
| Main Result | Positive |
| Result | We discovered differential SLC9A9 expression in different brain regions and identified 15 rs9828519-tagged SNPs that significantly regulated SLC9A9 expression only in occipital cortex, intralobular white matter, and substantia nigra. |
| Mechanism/Pathway | SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein families. |
