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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for HMX1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID3166
Official gene symbolHMX1
Full nameH6 family homeobox 1
Aliases,H6,NKX5-3,
Gene summaryThis 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]
LocationChromosome: 4   Locus: 4p16.1
Gene position8873543 - 8868773  Map Viewer
Gene orientationminus
Gene size4771 bp
Gene sequence
OMIM ID142992