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HMX1

Official Full Name
H6 family homeobox 1
Organism
Homo sapiens
GeneID
3166
Background
This gene encodes a transcription factor that belongs to the H6 family of homeobox proteins. This protein can bind a 5'-CAAG-3' core DNA sequence, and it is involved in the development of craniofacial structures. Mutations in this gene cause oculoauricular syndrome, a disorder of the eye and external ear. [provided by RefSeq, Oct 2009]
Synonyms
H6; NKX5-3;

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