WormBase Tree Display for Gene: WBGene00008877
expand all nodes | collapse all nodes | view schema
| WBGene00008877 | SMap | S_parent | Sequence | F16A11 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | rtcb-1 | Person_evidence | WBPerson236 | |||||
| Sequence_name | F16A11.2 | ||||||||
| Molecular_name | F16A11.2a | ||||||||
| F16A11.2a.1 | |||||||||
| CE23663 | |||||||||
| F16A11.2b | |||||||||
| Other_name | CELE_F16A11.2 | Accession_evidence | NDB | BX284601 | |||||
| Public_name | rtcb-1 | ||||||||
| DB_info | Database (12) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:49 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 28 Jan 2015 11:26:55 | WBPerson2970 | Name_change | CGC_name | rtcb-1 | ||||
| Status | Live | ||||||||
| Gene_info (10) | |||||||||
| Disease_info | Experimental_model | DOID:14330 | Homo sapiens | Paper_evidence | WBPaper00031384 | ||||
| WBPaper00046051 | |||||||||
| Curator_confirmed | WBPerson324 | ||||||||
| Date_last_updated | 24 Jul 2013 00:00:00 | ||||||||
| Disease_relevance | In an elegans model of Parkinson''s disease, where human alpha-synuclein was overexpressed, RNA interference studies showed that the elegans rtcb-1 (contains an RNA-binding motif, ortholog to human HSPC117 protein, a component of RNA trafficking granules in neurons), significantly protected against age- and dose-dependent degeneration in the dopamine neurons of transgenic worms; further the RNA ligase activity of rtcb-1 is required for neuroprotection, which is mediated via the splicing of the xbp-1/HAC1 mRNA in the unfolded protein response pathway; this model highlights the intersection of RNA processing and proteostasis in mediating neuroprotection; it also allows the identification of human modifier proteins of alpha-synuclein dependent misfolding and neurodegeneration, these proteins may also be new potential targets for therapeutic intervention. | Homo sapiens | Paper_evidence | WBPaper00031384 | |||||
| WBPaper00046051 | |||||||||
| Curator_confirmed | WBPerson324 | ||||||||
| Date_last_updated | 04 Feb 2015 00:00:00 | ||||||||
| Models_disease_in_annotation | WBDOannot00000215 | ||||||||
| Molecular_info | Corresponding_CDS | F16A11.2a | |||||||
| Corresponding_transcript | F16A11.2b | ||||||||
| F16A11.2a.1 | |||||||||
| Other_sequence (89) | |||||||||
| Experimental_info | RNAi_result | WBRNAi00003394 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00025118 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00076309 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00065397 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00025117 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00044772 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00008148 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00116595 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Chronogram686 | ||||||||
| Expr5773 | |||||||||
| Expr12080 | |||||||||
| Expr12738 | |||||||||
| Expr1018785 | |||||||||
| Expr1033870 | |||||||||
| Expr1148737 | |||||||||
| Expr2015570 | |||||||||
| Expr2033805 | |||||||||
| Drives_construct | WBCnstr00003232 | ||||||||
| Construct_product | WBCnstr00006218 | ||||||||
| WBCnstr00006225 | |||||||||
| WBCnstr00019835 | |||||||||
| WBCnstr00020144 | |||||||||
| WBCnstr00022738 | |||||||||
| WBCnstr00022739 | |||||||||
| Microarray_results (17) | |||||||||
| Expression_cluster (96) | |||||||||
| Interaction | WBInteraction000242604 | ||||||||
| WBInteraction000288404 | |||||||||
| WBInteraction000330452 | |||||||||
| WBInteraction000370713 | |||||||||
| WBInteraction000444571 | |||||||||
| WBInteraction000524592 | |||||||||
| Map_info | Map | I | Position | 3.75935 | |||||
| Positive | Positive_clone | F16A11 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference (13) | |||||||||
| 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 |
