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Gene: F20D12.5 
| F20D12.5 | SMap | S_parent | Sequence | F20D12 |
|---|---|---|---|---|
| Chromosome | IV | |||
| Identity (5) | ||||
| Gene_info (5) | ||||
| Molecular_info | Corresponding_CDS | F20D12.5 | ||
| Corresponding_protein | WP:CE29767 | |||
| Corresponding_RNAi_reagent | Cenix:132-d6 | |||
| mv_G_YK7761 | ||||
| Experimental_info | RNAi_result | Cenix:132-d6 | ||
| WB_RNAi_result | MV_SV:mv_G_YK7761 | |||
| Cenix:132-d6 | ||||
| Reference | WBPaper00003721 | |||
| WBPaper00012523 | ||||
| WBPaper00019619 | ||||
| WBPaper00026207 | ||||
| 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 | ||
| n2669 was previously listed as an allele of exc-5. Later repeated complementation tests showed n2669 to be an allele of a novel locus positioned close to exc-5. | ||||
| Method | Gene |
