Gene: T20H4.5
T20H4.5 | SMap | S_parent | Sequence | T20H4 | |
---|---|---|---|---|---|
Chromosome | III | ||||
Identity (5) | |||||
Gene_info | Allele | uCE3-992 | |||
GO_term | GO:0005489 | IEA | Inferred_automatically | ||
GO:0005506 | IEA | Inferred_automatically | |||
GO:0006118 | IEA | Inferred_automatically | |||
GO:0016651 | IEA | Inferred_automatically | |||
Contained_in_operon | CEOP3424 | ||||
Structured_description | Provisional_description (5) | ||||
Concise_description | The T20H4.5 gene encodes an ortholog of the human gene NADH DEHYDROGENASE-UBIQUINONE FE-S PROTEIN 8 23 KDA SUBUNIT; MITOCHONDRIAL COMPLEX I TYKY SUBUNIT (NDUFS8; OMIM:602141), which when mutated leads to Leigh syndrome (OMIM:256000); the T20H4.5 protein is predicted to be mitochondrial with 52% accuracy. | ||||
Molecular_info (5) | |||||
Experimental_info | RNAi_result | Cenix:305-c3 | |||
Cenix:341-d7 | |||||
JA:T20H4.5 | |||||
Simmer:T20H4.5 | |||||
TH:305C3 | |||||
TH:341D7 | |||||
WB_RNAi_result (7) | |||||
Y2H_bait | Y2H002209 | ||||
Y2H010877 | |||||
Y2H010878 | |||||
Reference | WBPaper00003662 | ||||
Method | Gene |