WormBase Tree Display for Gene: WBGene00021073
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| WBGene00021073 | SMap | S_parent | Sequence | CHROMOSOME_II | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 4 | |||||||
| Name | CGC_name | nsun-1 | Person_evidence | WBPerson3772 | |||||
| WBPerson38007 | |||||||||
| Sequence_name | W07E6.1 | ||||||||
| Molecular_name | W07E6.1a | ||||||||
| W07E6.1a.1 | |||||||||
| CE28259 | |||||||||
| W07E6.1b | |||||||||
| CE51106 | |||||||||
| W07E6.1b.1 | |||||||||
| Other_name | nol-1 | ||||||||
| nol-2 | |||||||||
| CELE_W07E6.1 | Accession_evidence | NDB | BX284602 | ||||||
| Public_name | nsun-1 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:31:04 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| 2 | 17 Aug 2007 14:29:26 | WBPerson2970 | Name_change | CGC_name | nol-1 | ||||
| 3 | 01 Aug 2017 12:58:54 | WBPerson2970 | Name_change | CGC_name | nol-2 | ||||
| Other_name | nol-1 | ||||||||
| 4 | 01 Jun 2020 11:19:49 | WBPerson1983 | Name_change | CGC_name | nsun-1 | ||||
| Other_name | nol-2 | ||||||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | nsun | ||||||||
| Allele (69) | |||||||||
| Strain | WBStrain00055474 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (28) | |||||||||
| Contained_in_operon | CEOP2028 | ||||||||
| CEOP2686 | |||||||||
| Ortholog (38) | |||||||||
| Paralog | WBGene00013151 | Caenorhabditis elegans | From_analysis | Panther | |||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Enables rRNA (cytosine-C5-)-methyltransferase activity. Involved in several processes, including negative regulation of cellular response to heat; negative regulation of locomotion involved in locomotory behavior; and positive regulation of reproductive process. Predicted to be located in nucleolus. Expressed widely. Used to study Williams-Beuren syndrome. Is an ortholog of human NOP2 (NOP2 nucleolar protein). | Paper_evidence | WBPaper00065943 | |||||
| WBPaper00067038 | |||||||||
| Curator_confirmed | WBPerson324 | ||||||||
| WBPerson37462 | |||||||||
| Inferred_automatically | This description was generated automatically by a script based on data from the WS296 version of WormBase | ||||||||
| Date_last_updated | 20 Mar 2025 00:00:00 | ||||||||
| Disease_info | Experimental_model | DOID:1928 | Homo sapiens | Paper_evidence | WBPaper00060738 | ||||
| Curator_confirmed | WBPerson324 | ||||||||
| Date_last_updated | 26 Aug 2021 00:00:00 | ||||||||
| Models_disease_in_annotation | WBDOannot00001017 | ||||||||
| Molecular_info | Corresponding_CDS | W07E6.1a | |||||||
| W07E6.1b | |||||||||
| Corresponding_transcript | W07E6.1a.1 | ||||||||
| W07E6.1b.1 | |||||||||
| Other_sequence | FK808924.1 | ||||||||
| Tcir_isotig02450 | |||||||||
| JI212929.1 | |||||||||
| Tcir_isotig02449 | |||||||||
| Acan_isotig18328 | |||||||||
| CBC09039_1 | |||||||||
| Associated_feature | WBsf665325 | ||||||||
| WBsf665326 | |||||||||
| WBsf986413 | |||||||||
| WBsf986414 | |||||||||
| WBsf1011398 | |||||||||
| WBsf222607 | |||||||||
| WBsf222608 | |||||||||
| Experimental_info | RNAi_result (22) | ||||||||
| Expr_pattern | Expr2052 | ||||||||
| Expr1027369 | |||||||||
| Expr1039192 | |||||||||
| Expr1158483 | |||||||||
| Expr2014349 | |||||||||
| Expr2032590 | |||||||||
| Microarray_results (23) | |||||||||
| Expression_cluster (146) | |||||||||
| Interaction (409) | |||||||||
| Map_info | Map | II | Position | -15.6042 | Error | 0.001006 | |||
| Positive | Positive_clone | W07E6 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00028451 | ||||||||
| WBPaper00029254 | |||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00060738 | |||||||||
| 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 |
