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Gene: F52B11.2 
| F52B11.2 | SMap | S_parent | Sequence | F52B11 | ||
|---|---|---|---|---|---|---|
| Chromosome | IV | |||||
| Identity (5) | ||||||
| Gene_info | GO_term | GO:0004615 | IEA | Inferred_automatically | ||
| GO:0019307 | IEA | Inferred_automatically | ||||
| GO:0005737 | IEA | Inferred_automatically | ||||
| Contained_in_operon | CEOP4576 | |||||
| Structured_description | Provisional_description | F52B11.2 is orthologous to the human gene PHOSPHOMANNOMUTASE 2 (PMS2; OMIM:601785), which when mutated leads to congenital disorder of glycosylation, type Ia. | Person_evidence | WBPerson567 | ||
| Curator_confirmed | WBPerson567 | |||||
| Concise_description | F52B11.2 is orthologous to the human gene PHOSPHOMANNOMUTASE 2 (PMS2; OMIM:601785), which when mutated leads to congenital disorder of glycosylation, type Ia. | |||||
| Molecular_info (6) | ||||||
| Experimental_info | RNAi_result | Cenix:61-g1 | ||||
| JA:F52B11.2 | ||||||
| [cgc5655]:F52B11.2 | ||||||
| [cgc5655]:daf-2:F52B11.2 | ||||||
| [cgc5655]:tph-1:F52B11.2 | ||||||
| [cgc5655]:tub-1:F52B11.2 | ||||||
| WB_RNAi_result (7) | ||||||
| Method | Gene |
