Homo sapiens Gene: HMX1
Summary
InnateDB Gene IDBG-227653.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HMX1
Gene Name H6 family homeobox 1
Synonyms H6; NKX5-3
Species Homo sapiens
Ensembl Gene ENSG00000215612
Encoded Proteins
H6 family homeobox 1
H6 family homeobox 1
H6 family homeobox 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
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]
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:8846076-8871817
Strand Reverse strand
Band p16.1
Transcripts
ENST00000400677 ENSP00000383516
ENST00000506970 ENSP00000446997
ENST00000617742 ENSP00000479086
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0007275 multicellular organismal development
GO:0045892 negative regulation of transcription, DNA-templated
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_018942 XM_005248160
HUGO
OMIM
CCDS CCDS47018
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas