EVX2 (even-skipped homeobox 2)

2014-11-01  

Identity

HGNC
LOCATION
2q31.1
LOCUSID
ALIAS
EVX-2

Other Information

Locus ID:

NCBI: 344191
MIM: 142991
HGNC: 3507
Ensembl: ENSG00000174279

Variants:

dbSNP: 344191
ClinVar: 344191
TCGA: ENSG00000174279
COSMIC: EVX2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000174279ENST00000308618Q03828

Expression (GTEx)

0
1
2
3
4
5
6
7
8

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
117781602002A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.19

Citation

Dessen P

EVX2 (even-skipped homeobox 2)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/62939/evx2