Bos taurus Gene: HMX1
Summary
InnateDB Gene IDBG-643493.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HMX1
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000031197
Encoded Proteins
H6 family homeobox 1
H6 family homeobox 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000215612:
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 6:106868232-106872198
Strand Reverse strand
Band
Transcripts
ENSBTAT00000044175 ENSBTAP00000041689
ENSBTAT00000056515 ENSBTAP00000051029
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:0006355 regulation of transcription, DNA-templated
GO:0045892 negative regulation of transcription, DNA-templated
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Homo sapiens
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL F1N765
UniProt Splice Variant
Entrez Gene 785113
UniGene
RefSeq XM_003582354 XM_003586228
HUGO HGNC:5017
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02018441
GenPept
RNA Seq Atlas 785113