Home Details
| Official Symbol of Gene | IGHM |
| Species | Homo sapiens |
| Entrez Gene ID | 3507 |
| Official Full Name | immunoglobulin heavy constant mu |
| Also known as | MU; VH; AGM1 |
| Gene Type | other |
| dbXrefs | Ensembl:ENSG00000211899 IMGT/GENE-DB:IGHM; MIM:147020; AllianceGenome:HGNC:5541 |
| Map Location | 14q32.33 |
| Variation Type | haplotypes |
| refSNP ID | N/A |
| Detected Sample | total genomic DNA |
| Sample Detail | extracted from venous blood. |
| Detected Method | RFLP |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 94 affected individuals identified as part of a local prevalence survey , 84 affected index twins included as part of a previously reported twin study and 159 controls. |
| Pubmed ID | 8568530 |
| Year | 1995 |
| Title | Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | No significant allelic or haplotypic association was observed.Linkage without a population association suggests that a gene encoded on 14q confers susceptibility to multiple sclerosis. |
| Mechanism/Pathway | N/A |

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