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Gene: Y54G9A.3 
| Y54G9A.3 | Evidence | CGC_data_submission | ||||
|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | Y54G9A | |||
| Chromosome | II | |||||
| Identity (5) | ||||||
| Gene_info | Gene_class | kqt | ||||
| Allele | aw1 | |||||
| tm542 | ||||||
| GO_term (9) | ||||||
| Structured_description | Provisional_description | The kqt-3 gene encodes a homolog of human KVLQT1, which when mutated leads to type 1 long QT syndrome (OMIM:192500). | Paper_evidence | WBPaper00004103 | ||
| Person_evidence | WBPerson567 | |||||
| Curator_confirmed | WBPerson567 | |||||
| Date_last_updated | 17 Jun 2004 00:00:00 | |||||
| Concise_description | The kqt-3 gene encodes a homolog of human KVLQT1, which when mutated leads to type 1 long QT syndrome (OMIM:192500). | |||||
| Molecular_info (6) | ||||||
| Experimental_info | RNAi_result | Cenix:26-g7 | ||||
| JA:Y54G9A.3 | ||||||
| WB_RNAi_result | JA:Y54G9A.3 | |||||
| MV_SV:mv_Y54G9A.3 | ||||||
| Cenix:26-g7 | ||||||
| Expr_pattern | Expr3236 | |||||
| Reference (5) | ||||||
| Remark | Sequence connection from [Wei A] | |||||
| 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 |
