GJB6 gap junction protein beta 6
Gene ID: 10804, updated on 27-Nov-2024Gene type: protein coding
Also known as: ED2; EDH; HED; CX30; HED2; DFNA3; ECTD2; DFNA3B; DFNB1B
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- Go to complete Gene record for GJB6
- Go to Variation Viewer for GJB6 variants
Summary
Gap junctions allow the transport of ions and metabolites between the cytoplasm of adjacent cells. They are formed by two hemichannels, made up of six connexin proteins assembled in groups. Each connexin protein has four transmembrane segments, two extracellular loops, a cytoplasmic loop formed between the two inner transmembrane segments, and the N- and C-terminus both being in the cytoplasm. The specificity of the gap junction is determined by which connexin proteins comprise the hemichannel. In the past, connexin protein names were based on their molecular weight, however the new nomenclature uses sequential numbers based on which form (alpha or beta) of the gap junction is present. This gene encodes one of the connexin proteins. Mutations in this gene have been found in some forms of deafness and in some families with hidrotic ectodermal dysplasia. [provided by RefSeq, Jul 2008]
Associated conditions
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Copy number response
Description |
---|
Copy number response Haploinsufficency No evidence available (Last evaluated 2014-01-30) ClinGen Genome Curation PageTriplosensitivity No evidence available (Last evaluated 2014-01-30) ClinGen Genome Curation Page |
Genomic context
- Location:
- 13q12.11
- Sequence:
- Chromosome: 13; NC_000013.11 (20221962..20232319, complement)
- Total number of exons:
- 6
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for GJB6 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- CCHMC - Human Genetics Mutation Database
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- Hereditary Hearing Loss Homepage
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- The Connexin-deafness homepage
- Variation ViewerRelated Variants
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