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RGD ID: 1592346
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc25a42
Name: solute carrier family 25, member 42
Acc ID: DOID:699
Term: mitochondrial myopathy
Definition: A myopathy that is characterized by mitochondrial dysfunction. (DO)
Definition Source(s): "DO" "DO", "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Slc25a42 ISOSLC25A42 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Mitochondrial MyopathiesPMID:25741868 PMID:26541337 PMID:29327420 PMID:29923093 PMID:30237576
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