Gene
rmnd1
- ID
- ZDB-GENE-050522-21
- Name
- required for meiotic nuclear division 1 homolog
- Symbol
- rmnd1 Nomenclature History
- Previous Names
-
- zgc:113022
- Type
- protein_coding_gene
- Location
- Chr: 17 Mapping Details/Browsers
- Description
- Predicted to be involved in positive regulation of mitochondrial translation. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 11. Orthologous to human RMND1 (required for meiotic nuclear division 1 homolog).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:113022 (1 image)
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 11 | Alliance | Combined oxidative phosphorylation deficiency 11 | 614922 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Domain of unknown function DUF155 | RMD1/Sad1-interacting |
|---|---|---|---|
|
UniProtKB:A0A8M9P054
|
410 | ||
|
UniProtKB:A0A8M6YTU2
|
217 | ||
|
UniProtKB:A0A8M6Z1I6
|
296 | ||
|
UniProtKB:A0A8M3AIN6
|
206 | ||
|
UniProtKB:Q501V2
|
410 |
Interactions and Pathways
No data available
Plasmids
No data available