BSX (brain specific homeobox)

2014-11-01  

Identity

HGNC
LOCATION
11q24.1
LOCUSID
ALIAS
BSX1

Other Information

Locus ID:

NCBI: 390259
MIM: 611074
HGNC: 20450
Ensembl: ENSG00000188909

Variants:

dbSNP: 390259
ClinVar: 390259
TCGA: ENSG00000188909
COSMIC: BSX

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000188909ENST00000343035Q3C1V8

Expression (GTEx)

0
1

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
188550242009Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).16

Citation

Dessen P

BSX (brain specific homeobox)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60821/bsx-(brain-specific-homeobox)