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. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 33. Is expressed in several structures, including alar plate midbrain region; digestive system; midbrain; musculature system; and segmental plate. 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