Gene: TARID

Alternate names for this Gene: EYA4-AS1

Gene Summary:

Gene is located in Chromosome: 6

Location in Chromosome : 6q23.2

Description of this Gene: TCF21 antisense RNA inducing promoter demethylation

Type of Gene: ncRNA

Gene: EYA4

Alternate names for this Gene: CMD1J|DFNA10

Gene Summary: This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, and it may be important for eye development, and for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, and innate immunity following DNA damage, cellular damage, and viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Gene is located in Chromosome: 6

Location in Chromosome : 6q23.2

Description of this Gene: EYA transcriptional coactivator and phosphatase 4

Type of Gene: protein-coding

rs797045088 in TARID;EYA4 gene and Deafness, Autosomal Dominant 10 PMID 11159937 2001 Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.