Gene
shq1
- ID
- ZDB-GENE-070112-1412
- Name
- SHQ1, H/ACA ribonucleoprotein assembly factor
- Symbol
- shq1 Nomenclature History
- Previous Names
-
- zgc:158255
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have unfolded protein binding activity. Predicted to be involved in box H/ACA snoRNP assembly. Predicted to localize to cytoplasm and nucleoplasm. Orthologous to human SHQ1 (SHQ1, H/ACA ribonucleoprotein assembly factor).
- Genome Resources
- 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
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
dystonia 35, childhood-onset | Alliance | ?Dystonia 35, childhood-onset | 619921 |
Neurodevelopmental disorder with dystonia and seizures | 619922 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | CS domain | HSP20-like chaperone | Protein Shq1 | Shq1, C-terminal domain | SHQ1-like, CS domain |
---|---|---|---|---|---|---|
UniProtKB:A1L1R0
|
585 | |||||
UniProtKB:A0A8M2BDH4
|
395 | |||||
UniProtKB:F1QC67
|
586 |
Interactions and Pathways
No data available
Plasmids
No data available