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 be involved in cytosolic ribosome assembly. Predicted to act upstream of or within adaptive immune response. Predicted to be located in mitochondrial matrix and plasma membrane. 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