mt-Atp6 - ATP synthase 6, mitochondrial Gene

Also Known as ATP6

Species: Rattus norvegicus (strain: BN/SsNHsdMCW)

Gene Type: protein coding
Gene ID: 26197

Summary

Predicted to contribute to proton-transporting ATP Synthase activity, rotational mechanism. Involved in aging and response to hyperoxia. Predicted to be integral component of membrane. Predicted to be part of 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. Orthologous to human MT-ATP6 (mitochondrially encoded ATP Synthase membrane subunit 6). [provided by Alliance of Genome Resources, Apr 2022]

mt-Atp6 Products (1)

mRNA Protein Name
YP_665634.1 ATP synthase F0 subunit 6 (mitochondrion) [Rattus norvegicus]

Gene Ontology

  • Biological Process
Biological Process GO Annotation Evidence References Source
involved in response to hyperoxia IEP
IEP: Inferred from expression pattern
18481000 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

ATPase subunit 6

  • ATP synthase F0 subunit 6

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08751 MT-ATP6 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens mt-Atp6 NCBI NCBI:4508