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Gene: F09G8.4 
| F09G8.4 | Evidence | CGC_data_submission | ||||
|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | F09G8 | |||
| Chromosome | III | |||||
| Identity (5) | ||||||
| Gene_info | Gene_class | ncr | ||||
| GO_term | GO:0008158 | IEA | Inferred_automatically | |||
| GO:0016020 | IEA | Inferred_automatically | ||||
| Structured_description | Provisional_description | ncr-2 encodes a homolog of human NPC1, which when mutated leads to Niemann-Pick disease, type C (OMIM:257220). | Paper_evidence | WBPaper00004637 | ||
| Person_evidence | WBPerson567 | |||||
| Curator_confirmed | WBPerson567 | |||||
| Date_last_updated | 17 Jun 2004 00:00:00 | |||||
| Concise_description | ncr-2 encodes a homolog of human NPC1, which when mutated leads to Niemann-Pick disease, type C (OMIM:257220). | |||||
| Molecular_info (5) | ||||||
| Experimental_info | RNAi_result | Cenix:302-f11 | ||||
| Cenix:302-g11 | ||||||
| JA:F09G8.4 | ||||||
| TH:302F11 | ||||||
| WB_RNAi_result | TH:302F11 | |||||
| JA:F09G8.4 | ||||||
| Cenix:302-f11 | ||||||
| Cenix:302-g11 | ||||||
| Expr_pattern | Expr3223 | |||||
| Reference | WBPaper00004265 | |||||
| WBPaper00004161 | ||||||
| WBPaper00023695 | ||||||
| WBPaper00005195 | ||||||
| WBPaper00017935 | ||||||
| WBPaper00018391 | ||||||
| WBPaper00019522 | ||||||
| WBPaper00024550 | ||||||
| WBPaper00019416 | ||||||
| WBPaper00024084 | ||||||
| WBPaper00024136 | ||||||
| WBPaper00026538 | ||||||
| WBPaper00024393 | ||||||
| Method | Gene |
