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Gene : PANX2 Homo sapiens

Name  ? pannexin 2 Cytological Location  22q13.33
Brief Description  pannexin 2
description  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 1 are abundantly expressed in central nervous system (CNS) and are coexpressed in various neuronal populations. Studies in Xenopus oocytes suggest that this protein alone and in combination with pannexin 1 may form cell type-specific gap junctions with distinct properties. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
  • synonyms:
  • hPANX2,
  • PX2,
  • hPANX2,
  • HGNC:8600,
  • OTTHUMG00000044649,
  • PANX2,
  • NM_052839,
  • uc003bjn.5,
  • PX2
  • identifiers:
  • 56666,
  • ENSG00000073150,
  • PANX2

Genome feature

Region: gene ? Length: 9565  
Location: 22:50170731-50180295 Cyto location: 22q13.33

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



736 SN Ps

4 Cross References

13 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results