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GRHL2

Official Full Name
grainyhead like transcription factor 2
Organism
Homo sapiens
GeneID
79977
Background
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).[provided by RefSeq, Mar 2009]
Synonyms
BOM; ECTDS; PPCD4; DFNA28; TFCP2L3;

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