GJD3

Gap junction delta-2 (GJD2), also known as connexin-36 (Cx36) or gap junction alpha-9 (GJA9), is a protein that in humans is encoded by the GJD2 gene.[5]

GJD3
Identifiers
AliasesGJD3, CX31.9, Cx30.2, GJA11, GJC1, gap junction protein delta 3
External IDsOMIM: 607425 MGI: 2384150 HomoloGene: 17530 GeneCards: GJD3
Gene location (Human)
Chr.Chromosome 17 (human)[1]
Band17q21.2Start40,360,652 bp[1]
End40,364,737 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

125111

353155

Ensembl

ENSG00000183153

ENSMUSG00000047197

UniProt

Q8N144

Q91YD1

RefSeq (mRNA)

NM_152219

NM_178596

RefSeq (protein)

NP_689343

NP_848711

Location (UCSC)Chr 17: 40.36 – 40.36 MbChr 11: 98.98 – 98.98 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

This gene is a member of the large family of connexins that are required for the formation of gap junctions. Six connexin monomers form a hemichannel, or connexon, on the cell surface. This connexon can interact with a connexon from a neighboring cell, thus forming a channel linking the cytoplasm of the 2 cells.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000183153 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000047197 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: gap junction protein".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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