WormBase Tree Display for Gene: WBGene00016013
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| WBGene00016013 | SMap | S_parent | Sequence | C23G10 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | ugt-66 | Person_evidence | WBPerson1818 | |||||
| Sequence_name | C23G10.6 | ||||||||
| Molecular_name | C23G10.6 | ||||||||
| C23G10.6.1 | |||||||||
| CE45015 | |||||||||
| Other_name | CELE_C23G10.6 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | ugt-66 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:30:56 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| 2 | 07 Jun 2018 14:30:09 | WBPerson1983 | Name_change | CGC_name | ugt-66 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | ugt | ||||||||
| Allele (30) | |||||||||
| Strain | WBStrain00047636 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00092948 | ||||||||
| 00092949 | |||||||||
| 00092950 | |||||||||
| 00092951 | |||||||||
| 00092952 | |||||||||
| 00092953 | |||||||||
| 00092954 | |||||||||
| 00092955 | |||||||||
| 00121706 | |||||||||
| Contained_in_operon | CEOP3826 | ||||||||
| Ortholog (93) | |||||||||
| 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 | C23G10.6 | |||||||
| Corresponding_CDS_history | C23G10.6:wp165 | ||||||||
| C23G10.6:wp214 | |||||||||
| Corresponding_transcript | C23G10.6.1 | ||||||||
| Other_sequence | CJC12136_1 | ||||||||
| Oden_isotig21949 | |||||||||
| EX563196.1 | |||||||||
| EX561522.1 | |||||||||
| PPC07649_1 | |||||||||
| CJC03587_1 | |||||||||
| Associated_feature | WBsf666977 | ||||||||
| WBsf226778 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00041012 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00005373 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00011052 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00029111 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1021099 | ||||||||
| Expr1145055 | |||||||||
| Expr2001011 | |||||||||
| Expr2019229 | |||||||||
| Drives_construct | WBCnstr00028386 | ||||||||
| Construct_product | WBCnstr00028386 | ||||||||
| Microarray_results (16) | |||||||||
| Expression_cluster (265) | |||||||||
| Interaction | WBInteraction000303914 | ||||||||
| WBInteraction000504120 | |||||||||
| WBInteraction000541045 | |||||||||
| Map_info | Map | III | Position | -1.40939 | |||||
| Positive | Positive_clone | C23G10 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00055090 | |||||||||
| WBPaper00055433 | |||||||||
| WBPaper00062838 | |||||||||
| 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 |
