Gene
nop56
- ID
- ZDB-GENE-040109-1
- Name
- NOP56 ribonucleoprotein homolog
- Symbol
- nop56 Nomenclature History
- Previous Names
-
- nol5a
- NOP56 (1)
- Type
- protein_coding_gene
- Location
- Chr: 21 Mapping Details/Browsers
- Description
- Predicted to enable snoRNA binding activity. Acts upstream of or within several processes, including central nervous system development; swimming behavior; and thigmotaxis. Predicted to be located in nucleolus. Predicted to be part of box C/D RNP complex and small-subunit processome. Is expressed in head and midbrain. Human ortholog(s) of this gene implicated in spinocerebellar ataxia type 36. Orthologous to human NOP56 (NOP56 ribonucleoprotein).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 17 figures from 4 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| spinocerebellar ataxia type 36 | Alliance | Spinocerebellar ataxia 36 | 614153 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Nop, C-terminal domain | Nop domain | Nop domain superfamily | NOSIC | Nucleolar protein Nop56/Nop58 |
|---|---|---|---|---|---|---|
|
UniProtKB:Q6DRE5
|
548 | |||||
|
UniProtKB:Q5BKV5
|
301 | |||||
|
UniProtKB:G1K2N3
|
110 | |||||
|
UniProtKB:Q6PH34
|
481 | |||||
|
UniProtKB:E7EZW9
|
142 | |||||
|
UniProtKB:Q6TEL4
|
494 |
Interactions and Pathways
No data available
Plasmids
No data available