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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 (3) | |||||
| Reference | WBPaper00003662 | ||||
| Method | Gene |
