Gene: LOC107986961

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

Gene: LOC107986962

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

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

rs1554579878 in LOC107986961;LOC107986962;GRHL2 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.