Gene
smc5
- ID
- ZDB-GENE-061013-288
- Name
- structural maintenance of chromosomes 5
- Symbol
- smc5 Nomenclature History
- Previous Names
-
- pufa (1)
- pum3
- wu:fb70d10
- wu:fi47h05
- zgc:152845
- zgc:66377
- Type
- protein_coding_gene
- Location
- Chr: 10 Mapping Details/Browsers
- Description
- Predicted to be involved in double-strand break repair via homologous recombination and sister chromatid cohesion. Predicted to localize to Smc5-Smc6 complex. Orthologous to human SMC5 (structural maintenance of chromosomes 5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Zhu et al., 2023
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 2 figures from Zhu et al., 2023
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Atelis syndrome 2 | 620185 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | P-loop containing nucleoside triphosphate hydrolase | Rad50/SbcC-type AAA domain | RecF/RecN/SMC, N-terminal |
|---|---|---|---|---|
|
UniProtKB:F1QEQ8
|
697 | |||
|
UniProtKB:E7F0W1
|
1073 |
Interactions and Pathways
No data available
Plasmids
No data available