XB-FEAT-983244: Difference between revisions
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[In Humans] Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] | |||
Latest revision as of 10:13, 22 August 2017
gsdme
This is the community wiki page for the gene gsdme please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature changes
08/21/2017 Human symbol has changed for genepage ID: 983244 From dfna5 to gsdme
Human symbol has changed for Entrez Gene: 1687. From DFNA5 to GSDME
Human name has changed for Entrez Gene: 1687. From DFNA5, deafness associated tumor suppressor to gasdermin E icere-1
summary from NCBI
[In Humans] Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]