Homo sapiens Gene: EVX2
Summary
InnateDB Gene IDBG-75652.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol EVX2
Gene Name even-skipped homeobox 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000174279
Encoded Proteins
even-skipped homeobox 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is located at the 5' end of the HOXD gene cluster on chromosome 2. The encoded protein is a homeobox transcription factor that is related to the protein encoded by the Drosophila even-skipped (eve) gene, a member of the pair-rule class of segmentation genes. A 117 kb microdeletion at the 5' end of the HOXD gene cluster, which includes this gene and the HOXD9-HOXD13 genes, causes synpolydactyly, a dominantly inherited disease resulting in limb malformation. [provided by RefSeq, Sep 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:176077472-176083913
Strand Reverse strand
Band q31.1
Transcripts
ENST00000308618 ENSP00000312385
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:0008150 biological_process
GO:0035108 limb morphogenesis
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.452341
RefSeq NM_001080458
HUGO
OMIM
CCDS CCDS33333
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas