Home Details
| Official Symbol of Gene | NCF1 |
| Species | Homo sapiens |
| Entrez Gene ID | 653361 |
| Official Full Name | neutrophil cytosolic factor 1 |
| Also known as | CGD1; NCF1A; NOXO2; p47phox; SH3PXD1A |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000158517 MIM:608512; AllianceGenome:HGNC:7660 |
| Map Location | 7q11.23 |
| Variation Type | marker |
| refSNP ID | D7S1870 |
| Detected Sample | brain and neural tissues |
| Sample Detail | N/A |
| Detected Method | PCR |
| Disease | MS |
| Disease subtype | N/A |
| Population | Finnish |
| Sample Size | 347 Finnish patients with MS and 714 unaffected family members |
| Pubmed ID | 30567305 |
| Year | 2018 |
| Title | Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | This analysis showed suggestive association signals for NCF1 and CYBB (lowest p = 0.038 and p = 0.013, respectively). |
| Mechanism/Pathway | N/A |

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