Gene

myo9ab

ID
ZDB-GENE-080424-6
Name
myosin IXAb
Symbol
myo9ab Nomenclature History
Previous Names
  • myo9a2 (1)
  • myo9al2
  • im:7155152
Type
protein_coding_gene
Location
Chr: 25 Mapping Details/Browsers
Description
Predicted to have several functions, including ATP binding activity; GTPase activator activity; and actin binding activity. Involved in axon extension and swimming behavior. Predicted to localize to several cellular components, including cell junction; growth cone; and myosin complex. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome. Orthologous to human MYO9A (myosin IXA).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from O'Connor et al., 2016
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from O'Connor et al., 2019
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With myo9ab Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Myasthenic syndrome, congenital, 24, presynaptic 618198
Associated With myo9ab Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein Length
UniProtKB:A0A8M9PH01 2343
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations