WormBase Tree Display for Gene: WBGene00021709
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| WBGene00021709 | SMap | S_parent | Sequence | Y49C4A | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | ugt-29 | Person_evidence | WBPerson1208 | |||||
| WBPerson655 | |||||||||
| Sequence_name | Y49C4A.8 | ||||||||
| Molecular_name | Y49C4A.8a | ||||||||
| Y49C4A.8a.1 | |||||||||
| CE26130 | |||||||||
| Y49C4A.8a.2 | |||||||||
| Y49C4A.8a.3 | |||||||||
| Y49C4A.8b | |||||||||
| Other_name | CELE_Y49C4A.8 | Accession_evidence | NDB | BX284605 | |||||
| Public_name | ugt-29 | ||||||||
| DB_info | Database (12) | ||||||||
| 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 | 10 Jun 2005 11:17:00 | WBPerson2970 | Name_change | CGC_name | ugt-29 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | ugt | ||||||||
| Allele (154) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00023001 | ||||||||
| 00023002 | |||||||||
| 00023003 | |||||||||
| 00023004 | |||||||||
| 00023005 | |||||||||
| 00023006 | |||||||||
| 00125960 | |||||||||
| Ortholog (85) | |||||||||
| Paralog (73) | |||||||||
| Structured_description | Automated_description | Predicted to enable UDP-glycosyltransferase activity. Predicted to be located in membrane. Expressed in pharynx; tail; and vulval muscle. 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 | Y49C4A.8a | |||||||
| Corresponding_CDS_history | Y49C4A.8b:wp248 | ||||||||
| Corresponding_transcript | Y49C4A.8b | ||||||||
| Y49C4A.8a.1 | |||||||||
| Y49C4A.8a.2 | |||||||||
| Y49C4A.8a.3 | |||||||||
| Other_sequence (12) | |||||||||
| Associated_feature | WBsf652452 | ||||||||
| WBsf652453 | |||||||||
| WBsf999192 | |||||||||
| WBsf233286 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00057000 | Inferred_automatically | RNAi_primary | |||||
| Expr_pattern | Expr12961 | ||||||||
| Expr1012994 | |||||||||
| Expr1039508 | |||||||||
| Expr1160447 | |||||||||
| Expr2017774 | |||||||||
| Expr2035912 | |||||||||
| Drives_construct | WBCnstr00038051 | ||||||||
| Microarray_results (26) | |||||||||
| Expression_cluster (238) | |||||||||
| Interaction | WBInteraction000030319 | ||||||||
| WBInteraction000542659 | |||||||||
| WBInteraction000575922 | |||||||||
| WBInteraction000585687 | |||||||||
| Map_info | Map | V | Position | -19.963 | |||||
| Positive | Positive_clone | Y49C4A | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00035429 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00049730 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00060797 | |||||||||
| WBPaper00064073 | |||||||||
| 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 |
