1. Gene
  2. JCHAIN - joining chain of multimeric IgA and IgM Gene

JCHAIN - joining chain of multimeric IgA and IgM Gene

Homo sapiens

Also known as IGJ; JCH; IGCJ

Gene ID: 3512 | Gene type: protein coding

About JCHAIN

Cytogenetic location: 4q13.3 Genomic coordinates (GRCh38): 4:70,655,541-70,666,508 (from NCBI)

This gene has 5 transcripts (splice variants) and 126 orthologues. Biased expression in colon (RPKM 2264.9), duodenum (RPKM 2014.1) and 10 other tissues.

Summary

Enables IgA binding activity and protein homodimerization activity. Contributes to several functions, including immunoglobulin receptor binding activity; peptidoglycan binding activity; and phosphatidylcholine binding activity. Involved in several processes, including defense response to other organism; glomerular filtration; and positive regulation of respiratory burst. Located in extracellular space. Part of monomeric IgA immunoglobulin complex; pentameric IgM immunoglobulin complex; and secretory dimeric IgA immunoglobulin complex. [provided by Alliance of Genome Resources, Apr 2022]

JCHAIN Products(1)

mRNA Protein Name
NM_144646.4 NP_653247.1 immunoglobulin J chain precursor

JCHAIN Protein Structure

Ig_J_chain

Ig_J_chain: Immunoglobulin J chain (24 - 159)

  • 0
  • 100
  • 159 a.a.
Protein Preferred Names Protein Names

immunoglobulin J chain

IgJ chain

Recombinant JCHAIN Proteins

Cat. No. Product Name Accession Purity
HY-P74842 IgJ Protein, Human (His) P01591/NP_653247.1 (Q23-D159) ≥95%

Related Diseases

Diseases Alias
Alpha Chain Disease

Seligmann'S Disease

Immunoproliferative Small Intestinal Disease

Mu Chain Disease

Mu-Chain Disease

Epiphyseal Chondrodysplasia, Miura Type

ECDM

Tall Stature-Scoliosis-Macrodactyly Of The Great Toes Syndrome

Miura Type Epiphyseal Chondrodysplasia

Tall Stature-Scoliosis-Macrodactyly Of The Halluces Syndrome

Tall Stature-Long Halluces-Multiple Extra-Epiphyses Syndrome

Chondrodysplasia, Epiphyseal, Miura Type

Immunoglobulin Alpha Deficiency

Iga Deficiency

Gamma-A-Globulin Deficiency

Immunoglobulin A Deficiency

Hodgkin'S Lymphoma, Lymphocytic-Histiocytic Predominance

Hodgkin Disease

Hodgkin Lymphoma, Lymphocyte-Rich

Hodgkin Lymphoma, Lymphocytic-Histiocytic Predominance

Hodgkin'S Disease, Lymphocyte Predominance

Lymphocyte Rich Hodgkin'S Disease

Lymphocyte Rich Classical Hodgkin Lymphoma

Heavy Chain Disease

Hcd

Ciliary Dyskinesia, Primary, 7

Primary Ciliary Dyskinesia 7

CILD7

Ciliary Dyskinesia, Primary, 7, With Or Without Situs Inversus

Primary Ciliary Dyskinesia 7 With Or Without Situs Inversus

Ics7

Immotile Cilia Syndrome 7

Dyskinesia, Ciliary, Primary, 7

Isolated Growth Hormone Deficiency

Congenital Ighd

Congenital Isolated Gh Deficiency

Congenital Isolated Growth Hormone Deficiency

Non-Acquired Isolated Growth Hormone Deficiency

Pituitary Dwarfism

Dwarfism, Pituitary

Isolated Somatotropin Deficiency

Isolated Congenital Growth Hormone Deficiency

Familial Isolated Growth Hormone Deficiency

Ighd

Dwarfism, Growth Hormone Deficiency

Growth Hormone Deficiency Dwarfism

Isolated Gh Deficiency

Isolated Hgh Deficiency

Isolated Human Growth Hormone Deficiency

Isolated Somatotropin Deficiency Disorder

Dwarfism Pituitary

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta JCHAIN VGNC VGNC:106622
Canis familiaris JCHAIN VGNC VGNC:42184
Rattus norvegicus JCHAIN RGD RGD:1310155
Felis catus JCHAIN VGNC VGNC:107339
Bos taurus JCHAIN VGNC VGNC:30373
Mus musculus JCHAIN MGD MGI:96493
Others JCHAIN NCBI