Home Details
| Official Symbol of Gene | MCAT |
| Species | Homo sapiens |
| Entrez Gene ID | 27349 |
| Official Full Name | malonyl-CoA-acyl carrier protein transacylase |
| Also known as | MT; MCT; MCT1; fabD; NET62; FASN2C |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000100294 MIM:614479; AllianceGenome:HGNC:29622 |
| Map Location | 22q13.2 |
| Variation Type | allele |
| refSNP ID | J* |
| Detected Sample | genomic DNA, blood or frozen tissue |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | RRMS,PPMS,SPMS |
| Population | Caucasians |
| Sample Size | 523 MS patients |
| Pubmed ID | 18708297 |
| Year | 2008 |
| Title | Association of common mitochondrial DNA variants with multiple sclerosis and systemic lupus erythematosus |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | The K haplotype shows association with MS after correction for multiple testing. |
| Mechanism/Pathway | N/A |

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