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HMX2

Official Full Name
H6 family homeobox 2
Organism
Homo sapiens
GeneID
3167
Background
The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]
Synonyms
H6L; Nkx5-2;

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