| Gene Symbol | HMX1 |
| Entrez Gene ID | 3166 |
| Full Name | H6 family homeobox 1 |
| Synonyms | H6,NKX5-3 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | Oculoauricular syndrome, 612109 (3) |







































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