GRHL2 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human GRHL2 wild-type allele is located in the vicinity of 8q22.3 and is approximately 186 kb in length. This allele, which encodes grainyhead-like protein 2 homolog protein, is involved in development and maintenance of epithelial tissues and neurulation. Mutation of the gene is associated with non-syndromic sensorineural deafness autosomal dominant type 28.
**Synonyms:** - AA404325 - AA834945 - AI224578 - BF675485 - BOM - DFNA28 - Deafness, Autosomal Dominant 28 Gene - ECTDS - FLJ13782 - FLJ38245 - Grainyhead Like Transcription Factor 2 wt Allele - Grainyhead, Drosophila, Homolog of, 2 Gene - Grainyhead-Like 2 (Drosophila) Gene - Grainyhead-Like 2 Gene - PPCD4 - TFCP2L3
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Cross-system equivalences0
No cross-system equivalences mapped for this node.