HMX2 H6 family homeobox 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 3167)
Symbol: HMX2
Full name: H6 family homeobox 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: H6L; Nkx5-2
Summary: 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]
Expression: Biased expression in kidney (RPKM 1.3) and duodenum (RPKM 0.1)
Orthologs: mouse
Gene size: 2537bp
Exon count: 2