XB-FEAT-6041437: Difference between revisions
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This is the community wiki page for the gene '' | 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 | |||
Latest revision as of 07:00, 20 July 2017
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