WormBase Tree Display for Gene: WBGene00018612
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| WBGene00018612 | SMap | S_parent | Sequence | CHROMOSOME_III | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 3 | |||||||
| Name | CGC_name | disl-2 | Person_evidence | WBPerson237 | |||||
| Sequence_name | F48E8.6 | ||||||||
| Molecular_name | F48E8.6 | ||||||||
| F48E8.6.1 | |||||||||
| CE45000 | |||||||||
| Other_name | susi-1 | Paper_evidence | WBPaper00050727 | ||||||
| Person_evidence | WBPerson6615 | ||||||||
| CELE_F48E8.6 | Accession_evidence | NDB | BX284603 | ||||||
| Public_name | disl-2 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:31:00 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| 2 | 25 Nov 2013 08:28:53 | WBPerson2970 | Name_change | CGC_name | disl-2 | ||||
| 3 | 13 Mar 2017 11:05:20 | WBPerson2970 | Name_change | Other_name | susi-1 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | disl | ||||||||
| Allele (48) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (21) | |||||||||
| Ortholog (38) | |||||||||
| Paralog | WBGene00001001 | Caenorhabditis elegans | From_analysis | Panther | |||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Predicted to enable 3'-5'-RNA exonuclease activity. Involved in regulation of cell fate specification and regulation of development, heterochronic. Predicted to be located in P-body. Human ortholog(s) of this gene implicated in Perlman syndrome and nephroblastoma. Is an ortholog of human DIS3L2 (DIS3 like 3'-5' exoribonuclease 2). | Paper_evidence | WBPaper00065943 | |||||
| Curator_confirmed | WBPerson324 | ||||||||
| WBPerson37462 | |||||||||
| Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
| Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
| Disease_info | Potential_model | DOID:2154 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:28648) | ||||
| DOID:0060476 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:28648) | ||||||
| Molecular_info | Corresponding_CDS | F48E8.6 | |||||||
| Corresponding_transcript | F48E8.6.1 | ||||||||
| Other_sequence (67) | |||||||||
| Associated_feature | WBsf645166 | ||||||||
| WBsf658939 | |||||||||
| WBsf992390 | |||||||||
| WBsf224922 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00108510 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00108770 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00047755 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00015254 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00108756 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00001897 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00005132 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00032490 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr13269 | ||||||||
| Expr1023993 | |||||||||
| Expr1038012 | |||||||||
| Expr1151587 | |||||||||
| Expr2010933 | |||||||||
| Expr2029172 | |||||||||
| Drives_construct | WBCnstr00026384 | ||||||||
| WBCnstr00039129 | |||||||||
| Construct_product | WBCnstr00026384 | ||||||||
| WBCnstr00039129 | |||||||||
| Microarray_results (21) | |||||||||
| Expression_cluster (91) | |||||||||
| Interaction (103) | |||||||||
| Map_info | Map | III | Position | -1.69294 | |||||
| Positive | Positive_clone | F48E8 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00041065 | |||||||||
| WBPaper00044211 | |||||||||
| WBPaper00046050 | |||||||||
| WBPaper00047168 | |||||||||
| WBPaper00049828 | |||||||||
| WBPaper00050727 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00060183 | |||||||||
| WBPaper00061983 | |||||||||
| Remark | 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 |
