Gene

myo18b

ID
ZDB-GENE-111111-8
Name
myosin XVIIIB
Symbol
myo18b Nomenclature History
Previous Names
  • fro
  • frozen (1)
  • schläfrig (1)
  • sig (1)
Type
protein_coding_gene
Location
Ambiguous Mapping Details/Browsers
Description
Predicted to have ATP binding activity; actin binding activity; and motor activity. Involved in sarcomerogenesis. Predicted to localize to myosin complex. Used to study myopathy. Is expressed in musculature system and somite border.
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
4 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
14 figures from 4 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With myo18b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Klippel-Feil syndrome 4 Alliance Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism 616549
Associated With myo18b Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Transcripts
Genome Browsers
No data available
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