Homo sapiens Gene: NKX3-2
Summary
InnateDB Gene IDBG-10163.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NKX3-2
Gene Name NK3 homeobox 2
Synonyms BAPX1; NKX3.2; NKX3B; SMMD
Species Homo sapiens
Ensembl Gene ENSG00000109705
Encoded Proteins
NK3 homeobox 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the NK family of homeobox-containing proteins. The encoded protein may play a role in skeletal development. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:13540830-13545050
Strand Reverse strand
Band p15.33
Transcripts
ENST00000382438 ENSP00000371875
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000978 RNA polymerase II core promoter proximal region sequence-specific DNA binding
GO:0001078 RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in negative regulation of transcription
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0043565 sequence-specific DNA binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0001501 skeletal system development
GO:0006355 regulation of transcription, DNA-templated
GO:0006366 transcription from RNA polymerase II promoter
GO:0007368 determination of left/right symmetry
GO:0031016 pancreas development
GO:0032331 negative regulation of chondrocyte differentiation
GO:0042474 middle ear morphogenesis
GO:0043066 negative regulation of apoptotic process
GO:0048513 organ development
GO:0048536 spleen development
GO:0048645 organ formation
GO:0048705 skeletal system morphogenesis
GO:0048706 embryonic skeletal system development
GO:0055123 digestive system development
GO:0060576 intestinal epithelial cell development
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt P78367
TrEMBL
UniProt Splice Variant
Entrez Gene 579
UniGene Hs.105941 Hs.590927
RefSeq NM_001189
HUGO HGNC:951
OMIM 602183
CCDS CCDS3410
HPRD
IMGT
EMBL AF005260 AF009801 AF009802 BC111966 U89845
GenPept AAB49696 AAB82783 AAB82784 AAC39536 AAI11967
RNA Seq Atlas 579