Gene
c1qbp
- ID
- ZDB-GENE-050417-408
- Name
- complement component 1, q subcomponent binding protein
- Symbol
- c1qbp Nomenclature History
- Previous Names
-
- fa14h03
- sb:cb785
- si:ch1073-329n19.2
- wu:fa14h03
- zgc:110137
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to have mRNA binding activity; mitochondrial ribosome binding activity; and translation activator activity. Predicted to be involved in positive regulation of mitochondrial translation. Predicted to localize to mitochondrion. Is expressed in several structures, including alar plate midbrain region; digestive system; midbrain; musculature system; and segmental plate. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 33. Orthologous to human C1QBP (complement C1q binding protein).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 5 figures from Thisse et al., 2001
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb785 (10 images)
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 |
|---|---|---|---|
| combined oxidative phosphorylation deficiency 33 | Alliance | Combined oxidative phosphorylation deficiency 33 | 617713 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial glycoprotein | Mitochondrial glycoprotein superfamily |
|---|---|---|---|
|
UniProtKB:F1R3F7
|
270 |
Interactions and Pathways
No data available
Plasmids
No data available