Gene
hccsb
- ID
- ZDB-GENE-000607-78
- Name
- holocytochrome c synthase b
- Symbol
- hccsb Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 24 Mapping Details/Browsers
- Description
- Predicted to have holocytochrome-c synthase activity. Predicted to be involved in cytochrome c-heme linkage. Predicted to localize to mitochondrion. Human ortholog(s) of this gene implicated in microphthalmia. Is expressed in several structures, including adaxial cell; alar plate midbrain region; immature eye; musculature system; and retina. Orthologous to human HCCS (holocytochrome c synthase).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 8 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:55778 (9 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 |
|---|---|---|---|
| linear skin defects with multiple congenital anomalies 1 | Alliance | Linear skin defects with multiple congenital anomalies 1 | 309801 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR000511 | Holocytochrome c/c1 synthase |
Domain Details Per Protein
| Protein | Length | Holocytochrome c/c1 synthase |
|---|---|---|
|
UniProtKB:Q803H2
|
269 |
Interactions and Pathways
No data available
Plasmids
No data available