Gene
myo18b
- ID
- ZDB-GENE-111111-8
- Name
- myosin XVIIIB
- Symbol
- myo18b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 10 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
-
- Alliance (1)
- Gene:100331349 (1)
- Note
- None
- Comparative Information
- All Expression Data
- 4 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 14 figures from 4 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
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 |
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Homologous_superfamily | IPR027417 | P-loop containing nucleoside triphosphate hydrolase |
Domain Details Per Protein
Protein | Length | P-loop containing nucleoside triphosphate hydrolase |
---|---|---|
UniProtKB:A0A8M6Z360
|
687 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance