Gene

map1b

ID
ZDB-GENE-130530-690
Name
microtubule-associated protein 1B
Symbol
map1b Nomenclature History
Previous Names
  • zmp:0000000687 (1)
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Involved in chordate embryonic development; microtubule cytoskeleton organization; and regulation of microtubule depolymerization. Is expressed in mesoderm; neural keel; and neural rod. Orthologous to human MAP1B (microtubule associated protein 1B).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Jayachandran et al., 2016
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
4 figures from Jayachandran et al., 2016
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With map1b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 83 Alliance ?Deafness, autosomal dominant 83 619808
Periventricular nodular heterotopia 9 618918
Associated With map1b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR026074 Microtubule associated protein 1
Domain Details Per Protein
Protein Length Microtubule associated protein 1
UniProtKB:B2ZZ14 2033
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations