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Gene: C47D12.2 
| C47D12.2 | SMap | S_parent | Sequence | C47D12 | ||
|---|---|---|---|---|---|---|
| Chromosome | II | |||||
| Identity (5) | ||||||
| Gene_info | Allele | uCE2-2023 | ||||
| Structured_description | Provisional_description | C47D12.2 encodes an ortholog of human FLJ20071/FLJ90130 (dymeclin, OMIM:607461, mutated in Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia), which has no obvious function in mass RNAi assays | Paper_evidence | WBPaper00005654 | ||
| WBPaper00013114 | ||||||
| WBPaper00013195 | ||||||
| WBPaper00013213 | ||||||
| Curator_confirmed | WBPerson567 | |||||
| Date_last_updated | 07 Jul 2004 00:00:00 | |||||
| Concise_description | C47D12.2 encodes an ortholog of human FLJ20071/FLJ90130 (dymeclin, OMIM:607461, mutated in Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia), which has no obvious function in mass RNAi assays | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | Cenix:201-d3 | ||||
| JA:C47D12.2 | ||||||
| WB_RNAi_result | JA:C47D12.2 | |||||
| MV_SV:mv_C47D12.2 | ||||||
| Cenix:201-d3 | ||||||
| Y2H_bait (86) | ||||||
| Y2H_target | Y2H009801 | |||||
| Y2H009804 | ||||||
| Method | Gene |
