BARX1 (BARX homeobox 1)

2019-05-01  

Identity

HGNC
LOCATION
9q22.32
LOCUSID
ALIAS
-

Other Information

Locus ID:

NCBI: 56033
MIM: 603260
HGNC: 955
Ensembl: ENSG00000131668

Variants:

dbSNP: 56033
ClinVar: 56033
TCGA: ENSG00000131668
COSMIC: BARX1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000131668ENST00000253968Q9HBU1
ENSG00000131668ENST00000401724Q9HBU1

Expression (GTEx)

0
10
20
30
40
50
60
70

References

Pubmed IDYearTitleCitations
189786782008Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.21
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.18
263835892015Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma.8
174866242007Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow up.3
294540952018An esophageal adenocarcinoma susceptibility locus at 9q22 also confers risk to esophageal squamous cell carcinoma by regulating the function of BARX1.3
302810992019Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.2
187087382008Barx1, growth factors and apoptosis in facial tissue of children with clefts.1

Citation

Dessen P

BARX1 (BARX homeobox 1)

Atlas Genet Cytogenet Oncol Haematol. 2019-05-01

Online version: http://atlasgeneticsoncology.org/gene/57980/barx1-(barx-homeobox-1)