WormBase Tree Display for Gene: WBGene00021352
expand all nodes | collapse all nodes | view schema
| WBGene00021352 | SMap | S_parent | Sequence | Y37E3 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | pcyt-2.1 | Person_evidence | WBPerson293 | |||||
| Sequence_name | Y37E3.11 | ||||||||
| Molecular_name (27) | |||||||||
| Other_name | CELE_Y37E3.11 | Accession_evidence | NDB | BX284601 | |||||
| Public_name | pcyt-2.1 | ||||||||
| DB_info | Database (13) | ||||||||
| 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 | 13 Nov 2017 15:54:28 | WBPerson1983 | Name_change | CGC_name | pcyt-2.1 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | pcyt | ||||||||
| Allele (158) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (16) | |||||||||
| Contained_in_operon | CEOP1036 | ||||||||
| Ortholog (39) | |||||||||
| Paralog | WBGene00016531 | Caenorhabditis elegans | From_analysis | TreeFam | |||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00017241 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| WBGene00021215 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| Structured_description | Automated_description | Predicted to enable ethanolamine-phosphate cytidylyltransferase activity. Predicted to be involved in phosphatidylethanolamine biosynthetic process. Predicted to be located in cytoplasm. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 82. Is an ortholog of human PCYT2 (phosphate cytidylyltransferase 2, ethanolamine). | 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:0112343 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:8756) | ||||
| Molecular_info | Corresponding_CDS | Y37E3.11a | |||||||
| Y37E3.11b | |||||||||
| Y37E3.11c | |||||||||
| Y37E3.11d | |||||||||
| Y37E3.11e | |||||||||
| Y37E3.11f | |||||||||
| Y37E3.11g | |||||||||
| Y37E3.11h | |||||||||
| Y37E3.11i | |||||||||
| Corresponding_CDS_history | Y37E3.11:wp185 | ||||||||
| Corresponding_transcript | Y37E3.11a.1 | ||||||||
| Y37E3.11b.1 | |||||||||
| Y37E3.11c.1 | |||||||||
| Y37E3.11d.1 | |||||||||
| Y37E3.11e.1 | |||||||||
| Y37E3.11f.1 | |||||||||
| Y37E3.11g.1 | |||||||||
| Y37E3.11h.1 | |||||||||
| Y37E3.11i.1 | |||||||||
| Other_sequence (54) | |||||||||
| Associated_feature (12) | |||||||||
| Experimental_info | RNAi_result | WBRNAi00001284 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00055928 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1015223 | ||||||||
| Expr1039320 | |||||||||
| Expr1159448 | |||||||||
| Expr2007263 | |||||||||
| Expr2025496 | |||||||||
| Microarray_results (18) | |||||||||
| Expression_cluster (107) | |||||||||
| Interaction (54) | |||||||||
| Map_info | Positive | Positive_clone | Y37E3 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | I | -11.8736 | |||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00042257 | |||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
