Gene
klc2
- ID
- ZDB-GENE-030131-2670
- Name
- kinesin light chain 2
- Symbol
- klc2 Nomenclature History
- Previous Names
-
- fc15b01
- wu:fc15b01
- wu:fj62c06
- zgc:162288
- Type
- protein_coding_gene
- Location
- Ambiguous Mapping Details/Browsers
- Description
- Predicted to have microtubule motor activity. Involved in swimming behavior. Predicted to localize to kinesin complex. Human ortholog(s) of this gene implicated in SPOAN syndrome. Orthologous to human KLC2 (kinesin light chain 2).
- Genome Resources
-
- Alliance (1)
- Gene:562365 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| SPOAN syndrome | Alliance | Spastic paraplegia, optic atrophy, and neuropathy | 609541 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Kinesin light chain | Kinesin light chain repeat | Tetratricopeptide-like helical domain superfamily | Tetratricopeptide repeat |
|---|---|---|---|---|---|
|
UniProtKB:A4IG65
|
618 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance