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Gene : PJVK Homo sapiens

Name  ? pejvakin Cytological Location  2q31.2
Brief Description  pejvakin
description  The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008]
  • synonyms:
  • BQ887979,
  • uc002umi.5,
  • deafness, autosomal recessive 59,
  • OTTHUMG00000154425,
  • HGNC:29502,
  • PJVK,
  • NM_001042702,
  • DFNB59,
  • BC020859,
  • DFNB59
  • identifiers:
  • 494513,
  • ENSG00000204311,
  • PJVK

Genome feature

Region: gene ? Length: 16958  
Location: 2:178450592-178467549 Cyto location: 2q31.2

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0 Pathways

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]


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Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer

Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

24 SN Ps

4 Cross References

14 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results