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 have snoRNA binding activity. Involved in heart development. Predicted to localize to box C/D snoRNP complex and small-subunit processome. Is expressed in midbrain. Human ortholog(s) of this gene implicated in spinocerebellar ataxia type 36. Orthologous to human NOP56 (NOP56 ribonucleoprotein).
- Genome Resources
- Note
- None
- All Expression Data
- 1 figure from Recher et al., 2013
- Cross-Species Comparison
- High Throughput Data
- No data available
- Thisse Expression Data
-
Wild Type Expression Summary
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 | Helix hairpin bin domain superfamily | NOP5, N-terminal | Nop, C-terminal domain | Nop domain | Nop domain superfamily | NOSIC |
---|---|---|---|---|---|---|---|
UniProtKB:Q6TEL4
|
494 | ||||||
UniProtKB:G1K2N3
|
110 | ||||||
UniProtKB:Q6PH34
|
481 | ||||||
UniProtKB:Q6DRE5
|
548 | ||||||
UniProtKB:Q5BKV5
|
301 | ||||||
UniProtKB:E7EZW9
|
142 |
Interactions and Pathways
No data available
Plasmids
No data available
- Gene Tree
- Ensembl