Home Details
| Official Symbol of Gene | P2RX7 |
| Species | Homo sapiens |
| Entrez Gene ID | 5027 |
| Official Full Name | purinergic receptor P2X 7 |
| Also known as | P2X7 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000089041 MIM:602566; AllianceGenome:HGNC:8537 |
| Map Location | 12q24.31 |
| Variation Type | SNP |
| refSNP ID | rs1718119 |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | N/A |
| Population | Northern Spain |
| Sample Size | MS patients and controls were 734 and 588 |
| Pubmed ID | 21906809 |
| Year | 2011 |
| Title | Gain-of-function of P2X7 receptor gene variants in multiple sclerosis |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Case-control analysis of selected SNPs of the P2X7 receptor gene in the whole cohort. |
| Mechanism/Pathway | N/A |

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