GJA10

Protein-coding gene in the species Homo sapiens
GJA10
Identifiers
AliasesGJA10, CX62, gap junction protein alpha 10
External IDsOMIM: 611924 MGI: 1339969 HomoloGene: 7733 GeneCards: GJA10
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)[1]
Chromosome 6 (human)
Genomic location for GJA10
Genomic location for GJA10
Band6q15Start89,894,469 bp[1]
End89,921,760 bp[1]
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)[2]
Chromosome 4 (mouse)
Genomic location for GJA10
Genomic location for GJA10
Band4 A5|4 14.25 cMStart32,596,960 bp[2]
End32,602,760 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • prefrontal cortex
Top expressed in
  • secondary oocyte

  • Region I of hippocampus proper

  • gland

  • adipose tissue

  • endocrine gland

  • white adipose tissue

  • haematopoietic system

  • thymus
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • gap junction channel activity
Cellular component
  • integral component of membrane
  • gap junction
  • cell junction
  • plasma membrane
  • connexin complex
  • membrane
Biological process
  • synapse assembly
  • cell communication
  • gamete generation
  • transmembrane transport
  • response to light stimulus
  • detection of light stimulus involved in visual perception
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

84694

14610

Ensembl

ENSG00000135355
ENSG00000288435

ENSMUSG00000051056

UniProt

Q969M2

Q9WUS4

RefSeq (mRNA)

NM_032602

NM_010289

RefSeq (protein)

NP_115991

NP_034419

Location (UCSC)Chr 6: 89.89 – 89.92 MbChr 4: 32.6 – 32.6 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Gap junction alpha-10 protein, also known as connexin-62 (Cx62), is a protein that in humans is encoded by the GJA10 gene.[5]

Connexins, such as GJA10, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits.[5][6]

References

  1. ^ a b c ENSG00000288435 GRCh38: Ensembl release 89: ENSG00000135355, ENSG00000288435 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000051056 – 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. ^ a b "Entrez Gene: gap junction protein".
  6. ^ Söhl G, Nielsen PA, Eiberger J, Willecke K (2003). "Expression profiles of the novel human connexin genes hCx30.2, hCx40.1, and hCx62 differ from their putative mouse orthologues". Cell Commun. Adhes. 10 (1): 27–36. doi:10.1080/15419060302063. PMID 12881038. S2CID 225894.

Further reading

  • Hosgood HD, Zhang L, Shen M, et al. (2009). "Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity". Occup Environ Med. 66 (12): 848–53. doi:10.1136/oem.2008.044024. PMC 2928224. PMID 19773279.

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

  • v
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Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl: Chloride channel
H+: Proton channel
M+: CNG cation channel
M+: TRP cation channel
H2O (+ solutes): Porin
Cytoplasm: Gap junction
By gating mechanism
Ion channel class
see also disorders


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