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Gene: mt-Atp6 (ATP synthase 6, mitochondrial) Mus musculus
Symbol: mt-Atp6
Name: ATP synthase 6, mitochondrial
Description: Predicted to contribute to ATPase activity and proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in ATP synthesis coupled proton transport. Localizes to the mitochondrion. 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 several structures, including alimentary system; brain; heart; integumental system; and sensory organ. Orthologous to human MT-ATP6 (mitochondrially encoded ATP synthase 6); PARTICIPATES IN electron transport chain pathway; Alzheimer's disease pathway; Huntington's disease pathway; INTERACTS WITH (+)-catechin; 2,3,7,8-tetrachlorodibenzodioxine; 3,4-methylenedioxymethamphetamine.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ATP synthase F0 subunit 6
Latest Assembly: GRCm38 - Mouse Genome Assembly GRCm38
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
GRCm38 EnsemblMT7,927 - 8,607 (+)Ensembl
GRCm38MT7,927 - 8,607 (+)NCBIGRCm38GRCm38mm10GRCm38
MGSCv37MT7,927 - 8,607 (+)NCBIGRCm37mm9NCBIm37
Cytogenetic MapMT NCBI

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated


Comparative Map Data
Position Markers
miRNA Target Status



Nucleotide Sequences
Protein Sequences

Additional Information

External Database Links
Nomenclature History
More on mt-Atp6
Alliance Gene
Ensembl Gene
MGI Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 736804
Created: 2004-02-06
Species: Mus musculus
Last Modified: 2019-11-27
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.