WormBase Tree Display for Gene: WBGene00045293
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| WBGene00045293 | SMap | S_parent | Sequence | C38D9 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | fbxa-175 | Person_evidence | WBPerson655 | |||||
| Sequence_name | C38D9.12 | ||||||||
| Molecular_name | C38D9.12 | ||||||||
| Other_name | CELE_C38D9.12 | Accession_evidence | NDB | BX284605 | |||||
| Public_name | fbxa-175 | ||||||||
| DB_info | Database | NDB | locus_tag | CELE_C38D9.12 | |||||
| NCBI | gene | 13217901 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 Feb 2007 15:02:48 | WBPerson4025 | Event | Split_from | WBGene00008017 | ||
| 2 | 01 Mar 2007 11:55:18 | WBPerson2970 | Name_change | CGC_name | fbxa-175 | ||||
| Split_from | WBGene00008017 | ||||||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0000336 | |||||||
| Gene_class | fbxa | ||||||||
| Allele (70) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| Paralog | WBGene00009296 | Caenorhabditis elegans | From_analysis | modENCODE_Pseudogenes | |||||
| Structured_description | Automated_description | Enriched in intestine based on RNA-seq studies. Is affected by several genes including hsf-1; clk-1; and npr-1 based on microarray and RNA-seq studies. Is affected by bortezomib based on RNA-seq studies. | 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 | ||||||||
| Molecular_info | Corresponding_pseudogene | C38D9.12 | |||||||
| Associated_feature | WBsf647660 | ||||||||
| Experimental_info | Microarray_results | GPL19516_CGZ0008160 | |||||||
| GPL21109_C38D9.12 | |||||||||
| GPL8673_C38D9_9P00758 | |||||||||
| Expression_cluster (27) | |||||||||
| Map_info | Map | V | Position | 12.9184 | Error | 5.5e-05 | |||
| Positive | Positive_clone | C38D9 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| 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 |
