Gene
hoxb1b
- ID
- ZDB-GENE-980526-290
- Name
- homeobox B1b
- Symbol
- hoxb1b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 12 Mapping Details/Browsers
- Description
- Exhibits sequence-specific DNA binding activity. Involved in several processes, including hindbrain development; neural keel formation; and regulation of histone modification. Predicted to localize to nucleus. Is expressed in several structures, including germ ring; mesoderm; neural keel; neural plate; and presumptive neural plate. Orthologous to human HOXB1 (homeobox B1).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 81 figures from 53 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb249 (16 images)
Wild Type Expression Summary
- All Phenotype Data
- 17 figures from 5 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Facial paresis, hereditary congenital, 3 | 614744 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Homeobox, conserved site | Homeobox domain | Homeobox domain, metazoa | Homeobox-like domain superfamily | Homeobox protein Hox-A1/B1/D1 |
---|---|---|---|---|---|---|
UniProtKB:Q90423
|
307 | |||||
UniProtKB:A3KNJ6
|
307 |
Type | Name | Length (nt) | Analysis |
---|---|---|---|
mRNA | hoxb1b-001 (1) | 1310 nt | |
mRNA |
hoxb1b-201
(1)
|
1606 nt |
Interactions and Pathways
No data available
Plasmids