Pannexin 1 is a protein in humans that is encoded by the PANX1 gene.[5]

Quick Facts Identifiers, Aliases ...
PANX1
Identifiers
AliasesPANX1, MRS1, PX1, UNQ2529, pannexin 1, OOMD7, Pannexin1
External IDsOMIM: 608420; MGI: 1860055; HomoloGene: 49416; GeneCards: PANX1; OMA:PANX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_015368

NM_019482

RefSeq (protein)

NP_056183

NP_062355

Location (UCSC)Chr 11: 94.13 – 94.18 MbChr 9: 14.91 – 14.96 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene belongs to the innexin family. Innexin family members are the structural components of gap junctions. This protein and pannexin 2 are abundantly expressed in central nerve system (CNS) and are coexpressed in various neuronal populations. Studies in Xenopus oocytes suggest that this protein alone and in combination with pannexin 2 may form cell type-specific gap junctions with distinct properties.[5]

Clinical relevance

Truncating mutations in this gene have been shown to promote breast cancer metastasis to the lungs by allowing cancer cells to survive mechanical stretch in the microcirculation.[6]

Disruptions of this gene have been associated to melanoma tumor progression.[7]

Pannexin 1 is also an important component of membrane channels involved in the formation of thin plasma membrane extensions called apoptopodia and beaded apoptopodia during apoptosis.[8][9]

References

Further reading

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