XB-FEAT-6041437

From XenWiki
Revision as of 07:00, 20 July 2017 by imported>Xenbase (→‎nomenclature changes)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

pjvk

This is the community wiki page for the gene pjvk please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase


summary from NCBI

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]

nomenclature changes

06/26/2017 Human symbol has changed for genepage ID: 6041437 From dfnb59 to pjvk

Human symbol has changed for Entrez Gene: 494513. From DFNB59 to PJVK

Human name has changed for Entrez Gene: 494513. From deafness, autosomal recessive 59 to pejvakin