WormBase Tree Display for Disease_model_annotation: WBDOannot00001332
expand all nodes | collapse all nodes | view schema
WBDOannot00001332 | Disease_term | DOID:700 | |
---|---|---|---|
Disease_of_species | Homo sapiens | ||
Modeled_by | Disease_relevant_gene | WBGene00009992 | |
Association_type | is_implicated_in | ||
Evidence_code | GO_code | IMP | |
ECO_term | ECO:0007013 | ||
Genetic_sex | hermaphrodite | ||
Paper_evidence | WBPaper00064182 | ||
Disease_model_description | Human 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_confirmed | WBPerson324 | ||
Date_last_updated | 11 Oct 2022 00:00:00 |