Bos taurus Gene: HOXD13
Summary
InnateDB Gene IDBG-640382.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HOXD13
Gene Name Uncharacterized protein
Synonyms HOXD13
Species Bos taurus
Ensembl Gene ENSBTAG00000004313
Encoded Proteins
homeobox D13
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 ENSG00000128714:
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008]
This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5\' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:20854099-20856159
Strand Reverse strand
Band
Transcripts
ENSBTAT00000005651 ENSBTAP00000005651
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003682 chromatin binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0001501 skeletal system development
GO:0006355 regulation of transcription, DNA-templated
GO:0007389 pattern specification process
GO:0009952 anterior/posterior pattern specification
GO:0022612 gland morphogenesis
GO:0030326 embryonic limb morphogenesis
GO:0030539 male genitalia development
GO:0035108 limb morphogenesis
GO:0042127 regulation of cell proliferation
GO:0042733 embryonic digit morphogenesis
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0060527 prostate epithelial cord arborization involved in prostate glandular acinus morphogenesis
GO:0060571 morphogenesis of an epithelial fold
GO:0060602 branch elongation of an epithelium
GO:0060687 regulation of branching involved in prostate gland morphogenesis
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL F1MT63
UniProt Splice Variant
Entrez Gene 100336775
UniGene Bt.32614
RefSeq XM_005197441
HUGO HGNC:5136
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02004174 DAAA02004175
GenPept
RNA Seq Atlas 100336775