Gene
mt-nd3
- ID
- ZDB-GENE-011205-9
- Name
- NADH dehydrogenase 3, mitochondrial
- Symbol
- mt-nd3 Nomenclature History
- Previous Names
-
- mtnd3
- ND3 (1)
- Type
- protein_coding_gene
- Location
- Chr: MT Mapping Details/Browsers
- Description
- Predicted to enable NADH dehydrogenase (ubiquinone) activity. Predicted to be involved in mitochondrial electron transport, NADH to ubiquinone. Predicted to be located in mitochondrial inner membrane. Predicted to be part of NADH dehydrogenase complex. Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; Leigh disease; and Parkinson's disease. Orthologous to human MT-ND3 (mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Sabharwal et al., 2018
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | NADH:ubiquinone oxidoreductase, subunit 3 superfamily | NADH:ubiquinone/plastoquinone oxidoreductase, chain 3 |
|---|---|---|---|
|
UniProtKB:Q9MIY3
|
116 |
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available