Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 3211
MIM: 142968
HGNC: 5111
Ensembl: ENSG00000120094
Variants:
dbSNP: 3211
ClinVar: 3211
TCGA: ENSG00000120094
COSMIC: HOXB1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000120094 | ENST00000239174 | P14653 |
| ENSG00000120094 | ENST00000577092 | P14653 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34488545 | 2021 | MicroRNA-301b-3p facilitates cell proliferation and migration in colorectal cancer by targeting HOXB1. | 5 |
| 34488545 | 2021 | MicroRNA-301b-3p facilitates cell proliferation and migration in colorectal cancer by targeting HOXB1. | 5 |
| 32102121 | 2020 | The MicroRNA hsa-let-7g Promotes Proliferation and Inhibits Apoptosis in Lung Cancer by Targeting HOXB1. | 11 |
| 32102121 | 2020 | The MicroRNA hsa-let-7g Promotes Proliferation and Inhibits Apoptosis in Lung Cancer by Targeting HOXB1. | 11 |
| 29923154 | 2018 | Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. | 1 |
| 29923154 | 2018 | Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. | 1 |
| 27640920 | 2017 | A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis. | 4 |
| 27640920 | 2017 | A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis. | 4 |
| 27144914 | 2016 | Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis. | 11 |
| 27144914 | 2016 | Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis. | 11 |
| 26565624 | 2015 | HOXB1 Is a Tumor Suppressor Gene Regulated by miR-3175 in Glioma. | 15 |
| 26565624 | 2015 | HOXB1 Is a Tumor Suppressor Gene Regulated by miR-3175 in Glioma. | 15 |
| 22770981 | 2012 | HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice. | 32 |
| 22770981 | 2012 | HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice. | 32 |
| 21433221 | 2011 | Anterior Hox genes interact with components of the neural crest specification network to induce neural crest fates. | 14 |
Citation
Dessen P
HOXB1 (homeobox B1)
Atlas Genet Cytogenet Oncol Haematol. 2016-08-01
Online version: http://atlasgeneticsoncology.org/gene/55862/hoxb1-(homeobox-b1)
