Gene: GRHL2

Alternate names for this Gene: BOM|DFNA28|ECTDS|PPCD4|TFCP2L3

Gene Summary: The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).

Gene is located in Chromosome: 8

Location in Chromosome : 8q22.3

Description of this Gene: grainyhead like transcription factor 2

Type of Gene: protein-coding

Gene: LOC107986961

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Gene: LOC107986962

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rs1554579819 in GRHL2;LOC107986961;LOC107986962 gene and Corneal dystrophy PMID 29499165 2018 Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4.