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Basic information of IGHM :

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

Sample information of multiple sclerosis:

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.

Literature information of multiple sclerosis :

Pubmed ID 8568530
Year 1995
Title Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region

Results of multiple sclerosis :

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