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Gene: T21B10.2 
| T21B10.2 | SMap | S_parent | Sequence | T21B10 | ||
|---|---|---|---|---|---|---|
| Chromosome | II | |||||
| Identity (5) | ||||||
| Gene_info | GO_term | GO:0004634 | IEA | Inferred_automatically | ||
| GO:0006096 | IEA | Inferred_automatically | ||||
| GO:0000015 | IEA | Inferred_automatically | ||||
| Contained_in_operon | CEOP2396 | |||||
| Structured_description | Provisional_description | T21B10.2 is orthologous to human ENOLASE 1 (also CRYSTALLIN, TAU; ENO1; OMIM:172430), which when mutated leads to spherocytic red cell enolase deficiency. | Person_evidence | WBPerson567 | ||
| Curator_confirmed | WBPerson567 | |||||
| Concise_description | T21B10.2 is orthologous to human ENOLASE 1 (also CRYSTALLIN, TAU; ENO1; OMIM:172430), which when mutated leads to spherocytic red cell enolase deficiency. | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | JA:T21B10.1 | ||||
| Simmer:T21B10.1 | ||||||
| JA:T21B10.2 | ||||||
| Cenix:72-h7 | ||||||
| Cenix:89-c1 | ||||||
| WB_RNAi_result (6) | ||||||
| Expr_pattern | Expr6382 | |||||
| Method | Gene |
