Homo sapiens Gene: GBX2
Summary
InnateDB Gene IDBG-84062.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GBX2
Gene Name gastrulation brain homeobox 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000168505
Encoded Proteins
gastrulation brain homeobox 2
gastrulation brain homeobox 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 2:236165236-236168369
Strand Reverse strand
Band q37.2
Transcripts
ENST00000306318 ENSP00000302251
ENST00000465889
ENST00000551105 ENSP00000448747
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:0001569 patterning of blood vessels
GO:0001755 neural crest cell migration
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007399 nervous system development
GO:0007411 axon guidance
GO:0008283 cell proliferation
GO:0021549 cerebellum development
GO:0021555 midbrain-hindbrain boundary morphogenesis
GO:0021568 rhombomere 2 development
GO:0021794 thalamus development
GO:0021884 forebrain neuron development
GO:0021930 cerebellar granule cell precursor proliferation
GO:0030902 hindbrain development
GO:0030917 midbrain-hindbrain boundary development
GO:0035239 tube morphogenesis
GO:0042472 inner ear morphogenesis
GO:0048483 autonomic nervous system development
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt P52951
TrEMBL
UniProt Splice Variant
Entrez Gene 2637
UniGene Hs.184945 Hs.735751
RefSeq NM_001485 XM_005246071
HUGO HGNC:4186
OMIM 601135
CCDS CCDS2515
HPRD 03087
IMGT
EMBL AC079135 AF118452 BC137448 BC137449 CH471063 U02080 U31468
GenPept AAA17406 AAC03241 AAD39907 AAI37449 AAI37450 AAX93240 EAW71084
RNA Seq Atlas 2637