WormBase Tree Display for Gene: WBGene00019234
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| WBGene00019234 | SMap | S_parent | Sequence | H23N18 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | ugt-8 | Person_evidence | WBPerson1208 | |||||
| WBPerson655 | |||||||||
| Sequence_name | H23N18.3 | ||||||||
| Molecular_name | H23N18.3 | ||||||||
| H23N18.3.1 | |||||||||
| CE20985 | |||||||||
| Other_name | CELE_H23N18.3 | Accession_evidence | NDB | BX284605 | |||||
| Public_name | ugt-8 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:31:01 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| 2 | 10 Jun 2005 11:17:00 | WBPerson2970 | Name_change | CGC_name | ugt-8 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | ugt | ||||||||
| Allele (42) | |||||||||
| Strain | WBStrain00003544 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00097327 | ||||||||
| 00097328 | |||||||||
| 00097329 | |||||||||
| 00097330 | |||||||||
| 00097331 | |||||||||
| 00097332 | |||||||||
| 00124133 | |||||||||
| Ortholog (120) | |||||||||
| Paralog (74) | |||||||||
| Structured_description | Automated_description | Predicted to enable UDP-glycosyltransferase activity. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in osteoporosis. Is an ortholog of several human genes including UGT2B10 (UDP glucuronosyltransferase family 2 member B10); UGT2B4 (UDP glucuronosyltransferase family 2 member B4); and UGT2B7 (UDP glucuronosyltransferase family 2 member B7). | 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:11476 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12547) | ||||
| Molecular_info | Corresponding_CDS | H23N18.3 | |||||||
| Corresponding_transcript | H23N18.3.1 | ||||||||
| Other_sequence | CSC01018_1 | ||||||||
| FD517098.1 | |||||||||
| FC542605.1 | |||||||||
| Acan_isotig08747 | |||||||||
| ACC06895_1 | |||||||||
| Acan_isotig09299 | |||||||||
| Associated_feature | WBsf646783 | ||||||||
| WBsf231711 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00033746 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00016304 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049468 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049469 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Chronogram495 | ||||||||
| Expr6282 | |||||||||
| Expr1011033 | |||||||||
| Expr1153194 | |||||||||
| Expr2017816 | |||||||||
| Expr2035953 | |||||||||
| Drives_construct | WBCnstr00003998 | ||||||||
| WBCnstr00025978 | |||||||||
| Construct_product | WBCnstr00025978 | ||||||||
| Microarray_results (16) | |||||||||
| Expression_cluster (255) | |||||||||
| Interaction (11) | |||||||||
| Map_info | Map | V | Position | -3.72696 | Error | 0.003016 | |||
| Positive | Positive_clone | H23N18 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00033099 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00044018 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00055433 | |||||||||
| WBPaper00061115 | |||||||||
| WBPaper00062515 | |||||||||
| WBPaper00064708 | |||||||||
| 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 |
