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Gene: VT23B5.2 
| VT23B5.2 | SMap | S_parent | Sequence | SUPERLINK_CB_IV | ||
|---|---|---|---|---|---|---|
| Chromosome | IV | |||||
| Identity (5) | ||||||
| Gene_info | Allele | ok912 | Inferred_automatically | From strain object: RB991 | ||
| Strain | RB991 | |||||
| GO_term | GO:0008270 | IEA | Inferred_automatically | |||
| Structured_description | Provisional_description | The VT23B5.2 gene encodes a homolog of human CHS, when when mutated leads to Chediak-Higashi syndrome (OMIM:214500). | Paper_evidence | WBPaper00004103 | ||
| Person_evidence | WBPerson567 | |||||
| Curator_confirmed | WBPerson567 | |||||
| Date_last_updated | 17 Jun 2004 00:00:00 | |||||
| Concise_description | The VT23B5.2 gene encodes a homolog of human CHS, when when mutated leads to Chediak-Higashi syndrome (OMIM:214500). | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | Cenix:38-d3 | ||||
| JA:VT23B5.2 | ||||||
| WB_RNAi_result | JA:VT23B5.2 | |||||
| MV_SV:mv_VT23B5.2 | ||||||
| Cenix:38-d3 | ||||||
| Method | Gene |
