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Gene: C49D10.9 
| C49D10.9 | SMap | S_parent | Sequence | C49D10 | |
|---|---|---|---|---|---|
| Chromosome | II | ||||
| Identity (5) | |||||
| Gene_info | Gene_class | nhr | |||
| Allele | tm895 | ||||
| GO_term | GO:0003700 | IEA | Inferred_automatically | ||
| GO:0006355 | IEA | Inferred_automatically | |||
| GO:0005634 | IEA | Inferred_automatically | |||
| Molecular_info (5) | |||||
| Experimental_info | RNAi_result | Cenix:204-a9 | |||
| JA:C49D10.9 | |||||
| WB_RNAi_result | JA:C17A2.1 | ||||
| MV_SV:mv_C17A2.1 | |||||
| Cenix:204-a9 | |||||
| JA:C49D10.9 | |||||
| Remark | Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC. | CGC_data_submission | |||
| Method | Gene |
