The following gene names and symbols are associated with antigen Deafness, Autosomal Dominant 5 across different species:

deafness, autosomal dominant 5 (DFNA5), deafness, autosomal dominant 5 (human) (Dfna5), deafness, autosomal dominant 5 (dfna5)

Other aliases include:

ICERE-1, Fin15, Dfna5h, EG14210, 2310037D07Rik, 4932441K13Rik, fk59f08, zgc:91916, wu:fc41e05, wu:fk59f08, MGC83660

On the protein level the following designations are being used for antigen Deafness, Autosomal Dominant 5:

deafness, autosomal dominant 5 protein – OTTHUMP00000202026 – nonsyndromic hearing impairment protein – inversely correlated with estrogen receptor expression 1 – deafness, autosomal dominant 5 homolog – deafness, autosomal dominant 5

Deafness, Autosomal Dominant 5 fulfills a number of functions:

protein binding – molecular_function

Deafness, Autosomal Dominant 5 is relevant to the following processes:

inner ear receptor cell differentiation – sensory perception of sound – ear morphogenesis – inner ear morphogenesis – regulation of biosynthetic process – biological_process

Locations for Deafness, Autosomal Dominant 5:

cellular_component

Source: NCBI Entrez Gene, Gene Ontology