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Gene: F57B10.6 
| F57B10.6 | SMap | S_parent | Sequence | F57B10 | ||
|---|---|---|---|---|---|---|
| Chromosome | I | |||||
| Identity (5) | ||||||
| Gene_info | Allele | tm1670 | ||||
| tm1682 | ||||||
| GO_term | GO:0003677 | IEA | Inferred_automatically | |||
| GO:0004518 | IEA | Inferred_automatically | ||||
| GO:0006281 | IEA | Inferred_automatically | ||||
| Contained_in_operon | CEOP1336 | |||||
| Structured_description | Provisional_description | F57B10.6 is orthologous to the human gene EXCISION REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 5 (XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G (COCKAYNE SYNDROME)) (ERCC5; OMIM:133530), which when mutated leads to disease. | Person_evidence | WBPerson567 | ||
| Curator_confirmed | WBPerson567 | |||||
| Concise_description | F57B10.6 is orthologous to the human gene EXCISION REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION GROUP 5 (XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G (COCKAYNE SYNDROME)) (ERCC5; OMIM:133530), which when mutated leads to disease. | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | Cenix:12-h12 | ||||
| JA:F57B10.6 | ||||||
| PF:GL1_2G12 | ||||||
| WB_RNAi_result | JA:F57B10.6 | |||||
| MV_SV:mv_F57B10.6 | ||||||
| Cenix:12-h12 | ||||||
| PF:GL1_2G12 | ||||||
| Method | Gene |
