GJB7

Protein-coding gene in the species Homo sapiens
GJB7
Identifiers
AliasesGJB7, CX25, bA136M9.1, connexin25, gap junction protein beta 7
External IDsOMIM: 611921 HomoloGene: 89311 GeneCards: GJB7
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)[1]
Chromosome 6 (human)
Genomic location for GJB7
Genomic location for GJB7
Band6q14.3-q15Start87,282,980 bp[1]
End87,329,278 bp[1]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right uterine tube

  • placenta

  • pituitary gland

  • anterior pituitary

  • right lung

  • bone marrow

  • endometrium

  • Achilles tendon

  • thymus

  • urinary bladder
    n/a
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
  • cell communication
  • transmembrane transport
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

375519

n/a

Ensembl

ENSG00000164411

n/a

UniProt

Q6PEY0

n/a

RefSeq (mRNA)

NM_198568

n/a

RefSeq (protein)

NP_940970

n/a

Location (UCSC)Chr 6: 87.28 – 87.33 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Gap junction beta-7 protein (GJB7), also known as connexin-25 (Cx25), is a protein that in humans is encoded by the GJB7 gene.[3]

Function

Connexins, such as GJB7, 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.[3][4]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000164411 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ a b "Entrez Gene: gap junction protein".
  4. ^ 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.

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


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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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