1. Gene
  2. Gsdme - gasdermin E Gene

Gsdme - gasdermin E Gene

Mus musculus

Also known as Dfna5; Fin15; Dfna5h; EG14210; 2310037D07Rik; 4932441K13Rik

Gene ID: 54722 | Gene type: protein coding

About Gsdme

Summary

Enables cardiolipin binding activity. Involved in cellular response to virus and necrotic cell death. Acts upstream of or within inner ear receptor cell differentiation. Located in cytoplasm. Is expressed in several structures, including alimentary system; brain; genitourinary system; hemolymphoid system gland; and liver and biliary system. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 5 and sensorineural hearing loss. Orthologous to human GSDME (gasdermin E). [provided by Alliance of Genome Resources, Apr 2022]

Gsdme Products(1)

mRNA Protein Name
NM_018769.4 NP_061239.1 gasdermin-E precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables cardiolipin binding IDA
IDA: Inferred from direct assay
28459430 MGI
Biological Process GO Annotation Evidence Reference Source
involved in cellular response to virus IMP
IMP: Inferred from mutant phenotype
28045099 MGI
acts upstream of or within inner ear auditory receptor cell differentiation IMP
IMP: Inferred from mutant phenotype
16023581 MGI
involved in pyroptotic inflammatory response IMP
IMP: Inferred from mutant phenotype
28045099 MGI
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
28209736 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

gasdermin-E

deafness associated tumor suppressor

deafness, autosomal dominant 5 homolog

non-syndromic hearing impairment protein 5 homolog

Orthologs Information

Species Symbol Source ID
Homo sapiens Gsdme NCBI NCBI:1687