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WormBase Tree Display for Disease_model_annotation: WBDOannot00001332

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Name Class

WBDOannot00001332Disease_termDOID:700
Disease_of_speciesHomo sapiens
Modeled_byDisease_relevant_geneWBGene00009992
Association_typeis_implicated_in
Evidence_codeGO_codeIMP
ECO_termECO:0007013
Genetic_sexhermaphrodite
Paper_evidenceWBPaper00064182
Disease_model_descriptionHuman NDUFV2 (NADH:ubiquinone oxidoreductase core subunit V2) is implicated in Complex I deficiency and susceptibility to Parkinson's disease. RNAi silencing of the C. elegans ortholog, F53F4.10, results in developmental phenotypes such as slow development and arrested L2/L3 larvae.
Curator_confirmedWBPerson324
Date_last_updated11 Oct 2022 00:00:00