Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 3507
MIM: 147020
HGNC: 5541
Ensembl: ENSG00000211899
IMGT/GENE-DB:
Variants:
dbSNP: 3507
ClinVar: 3507
TCGA: ENSG00000211899
COSMIC: IGHM
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000211899 | ENST00000390559 | P01871 |
| ENSG00000211899 | ENST00000637539 | P01871 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35048256 | 2022 | Association of IGHM polymorphisms with susceptibility to type 1 diabetes. | 2 |
| 35048256 | 2022 | Association of IGHM polymorphisms with susceptibility to type 1 diabetes. | 2 |
| 34057235 | 2021 | Intrathecal Immunoglobulin M Synthesis is an Independent Biomarker for Higher Disease Activity and Severity in Multiple Sclerosis. | 12 |
| 34409913 | 2021 | Screening differentially expressed genes between endometriosis and ovarian cancer to find new biomarkers for endometriosis. | 13 |
| 34435697 | 2021 | Refractory serum immunoglobulin M elevation during anti-interleukin (IL)-1- or IL-6-targeted treatment in four patients with Schnitzler syndrome. | 3 |
| 34057235 | 2021 | Intrathecal Immunoglobulin M Synthesis is an Independent Biomarker for Higher Disease Activity and Severity in Multiple Sclerosis. | 12 |
| 34409913 | 2021 | Screening differentially expressed genes between endometriosis and ovarian cancer to find new biomarkers for endometriosis. | 13 |
| 34435697 | 2021 | Refractory serum immunoglobulin M elevation during anti-interleukin (IL)-1- or IL-6-targeted treatment in four patients with Schnitzler syndrome. | 3 |
| 28534223 | 2017 | Immunoglobulin M gene association with autoantibody reactivity and type 1 diabetes. | 3 |
| 28769069 | 2017 | Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene. | 5 |
| 28534223 | 2017 | Immunoglobulin M gene association with autoantibody reactivity and type 1 diabetes. | 3 |
| 28769069 | 2017 | Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene. | 5 |
| 26910880 | 2016 | Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects. | 6 |
| 27611867 | 2016 | The Expression Pattern of the Pre-B Cell Receptor Components Correlates with Cellular Stage and Clinical Outcome in Acute Lymphoblastic Leukemia. | 18 |
| 26910880 | 2016 | Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects. | 6 |
Citation
Dessen P
IGHM (immunoglobulin heavy constant mu)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/45610/ighm
