Gene
mt-atp6
- ID
- ZDB-GENE-011205-18
- Name
- ATP synthase 6, mitochondrial
- Symbol
- mt-atp6 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: MT Mapping Details/Browsers
- Description
- Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in ATP synthesis coupled proton transport. Predicted to localize to mitochondrial proton-transporting ATP synthase complex. Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; NARP syndrome; Parkinson's disease; multiple sclerosis; and systemic lupus erythematosus. Is expressed in female organism. Orthologous to human MT-ATP6 (mitochondrially encoded ATP synthase membrane subunit 6).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 6 figures from 6 publications
- 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
| Type | InterPro ID | Name |
|---|---|---|
| Active_site | IPR023011 | ATP synthase, F0 complex, subunit A, active site |
| Family | IPR000568 | ATP synthase, F0 complex, subunit A |
| Family | IPR045083 | ATP synthase, F0 complex, subunit A, bacterial/mitochondria |
| Homologous_superfamily | IPR035908 | ATP synthase, F0 complex, subunit A superfamily |
Domain Details Per Protein
| Protein | Length | ATP synthase, F0 complex, subunit A | ATP synthase, F0 complex, subunit A, active site | ATP synthase, F0 complex, subunit A, bacterial/mitochondria | ATP synthase, F0 complex, subunit A superfamily |
|---|---|---|---|---|---|
|
UniProtKB:A0A0A0VDB1
|
227 | ||||
|
UniProtKB:Q9MIY5
|
227 |
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available