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Gene: T22B11.5 
| T22B11.5 | SMap | S_parent | Sequence | T22B11 | |
|---|---|---|---|---|---|
| Chromosome | IV | ||||
| Identity (5) | |||||
| Gene_info | GO_term | GO:0004591 | IEA | Inferred_automatically | |
| GO:0030976 | IEA | Inferred_automatically | |||
| GO:0006096 | IEA | Inferred_automatically | |||
| GO:0016624 | IEA | Inferred_automatically | |||
| GO:0008152 | IEA | Inferred_automatically | |||
| Structured_description | Provisional_description (5) | ||||
| Concise_description | The T22B11.5 gene encodes an ortholog of the human gene OGDH, which when mutated leads to alpha-ketoglutarate deficiency (OMIM:203740); the T22B11.5 protein is predicted to be mitochondrial with 68% accuracy. | ||||
| Molecular_info (5) | |||||
| Experimental_info | RNAi_result (7) | ||||
| WB_RNAi_result (9) | |||||
| Expr_pattern | Expr2111 | ||||
| Expr5147 | |||||
| Method | Gene |
