Gene

hoxb1a

ID
ZDB-GENE-990415-101
Name
homeobox B1a
Symbol
hoxb1a Nomenclature History
Previous Names
  • hoxb1
  • etID309950.3 (1)
  • id:ibd3532
  • sb:eu402
  • Z-3
Type
protein_coding_gene
Location
Chr: 3 Mapping Details/Browsers
Description
Exhibits sequence-specific DNA binding activity. Involved in central nervous system development. Predicted to localize to nucleus. Is expressed in several structures, including hindbrain; mesoderm; neural keel; neural plate; and neural rod. Orthologous to human HOXB1 (homeobox B1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
96 figures from 63 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
15 figures from 5 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With hoxb1a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Facial paresis, hereditary congenital, 3 614744
Associated With hoxb1a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Conserved_site IPR017970 Homeobox, conserved site
Domain IPR001356 Homeobox domain
Domain IPR020479 Homeobox domain, metazoa
Homologous_superfamily IPR009057 Homeobox-like domain superfamily
Domain Details Per Protein
Protein Length Homeobox, conserved site Homeobox domain Homeobox domain, metazoa Homeobox-like domain superfamily
UniProtKB:O42366 311
UniProtKB:B3DHZ4 316
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations