Homo sapiens Protein: HOXB2
Summary
InnateDB Protein IDBP-56723.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HOXB2
Protein Name homeobox B2
Synonyms Hox-2.8; HOX2; HOX2H; K8;
Species Homo sapiens
Ensembl Protein ENSP00000331741
InnateDB Gene IDBG-56721 (HOXB2)
Protein Structure
UniProt Annotation
Function Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. {ECO:0000269PubMed:10595394}.
Subcellular Localization Nucleus.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 2 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
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:0002011 morphogenesis of an epithelial sheet
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007275 multicellular organismal development
GO:0008015 blood circulation
GO:0009952 anterior/posterior pattern specification
GO:0009953 dorsal/ventral pattern formation
GO:0021569 rhombomere 3 development
GO:0021570 rhombomere 4 development
GO:0021612 facial nerve structural organization
GO:0048704 embryonic skeletal system morphogenesis
GO:0048705 skeletal system morphogenesis
GO:0048857 neural nucleus development
Cellular Component
GO:0005634 nucleus
Protein Structure and Domains
PDB ID
InterPro IPR001356 Homeobox domain
IPR009057 Homeodomain-like
IPR020479 Homeodomain, metazoa
PFAM PF00046
PRINTS PR00024
PIRSF
SMART SM00389
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P14652
PhosphoSite PhosphoSite-P14652
TrEMBL D3DTV2
UniProt Splice Variant
Entrez Gene 3212
UniGene Hs.738483
RefSeq NP_002136
HUGO HGNC:5113
OMIM 142967
CCDS CCDS11527
HPRD 00854
IMGT
EMBL BC074805 BC074806 CH471109 X14571 X16176 X16665 X78978
GenPept AAH74805 AAH74806 CAA32709 CAA34298 CAA34655 CAA55581 EAW94744 EAW94745