WormBase Tree Display for Gene: WBGene00022420
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| WBGene00022420 | SMap | S_parent | Sequence | Y102E9 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | wdr-4 | Person_evidence | WBPerson24179 | |||||
| Sequence_name | Y102E9.2 | ||||||||
| Molecular_name | Y102E9.2a | ||||||||
| Y102E9.2a.1 | |||||||||
| CE07574 | |||||||||
| Y102E9.2b | |||||||||
| CE41711 | |||||||||
| Y102E9.2b.1 | |||||||||
| Other_name | CELE_Y102E9.2 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | wdr-4 | ||||||||
| DB_info | Database (12) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:31:05 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| 2 | 28 Sep 2016 15:57:39 | WBPerson2970 | Name_change | CGC_name | wdr-4 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | wdr | ||||||||
| Allele (29) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00021227 | ||||||||
| 00021228 | |||||||||
| 00021229 | |||||||||
| 00021230 | |||||||||
| 00021231 | |||||||||
| 00077690 | |||||||||
| 00077691 | |||||||||
| 00077692 | |||||||||
| 00077693 | |||||||||
| 00126538 | |||||||||
| Contained_in_operon | CEOP3400 | ||||||||
| Ortholog (33) | |||||||||
| Structured_description | Automated_description | Predicted to be involved in tRNA modification. Predicted to be located in cytosol and nucleus. Predicted to be part of tRNA methyltransferase complex. Human ortholog(s) of this gene implicated in Galloway-Mowat syndrome and microcephaly, growth deficiency, seizures, and brain malformations. Is an ortholog of human WDR4 (WD repeat domain 4). | 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:0080694 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12756) | ||||
| DOID:0081051 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12756) | ||||||
| Molecular_info | Corresponding_CDS | Y102E9.2a | |||||||
| Y102E9.2b | |||||||||
| Corresponding_CDS_history | Y102E9.2:wp183 | ||||||||
| Corresponding_transcript | Y102E9.2a.1 | ||||||||
| Y102E9.2b.1 | |||||||||
| Other_sequence | Acan_isotig06647 | ||||||||
| CRC07369_1 | |||||||||
| ACC06704_1 | |||||||||
| PPC08389_1 | |||||||||
| EY468956.1 | |||||||||
| Oden_isotig15414 | |||||||||
| CBC06574_1 | |||||||||
| CR00573 | |||||||||
| CRC08674_1 | |||||||||
| Associated_feature | WBsf659090 | ||||||||
| WBsf976178 | |||||||||
| WBsf976179 | |||||||||
| WBsf976180 | |||||||||
| WBsf225147 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00036457 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00019823 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00055158 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00005553 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00007652 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1015034 | ||||||||
| Expr1039902 | |||||||||
| Expr1158688 | |||||||||
| Expr2018056 | |||||||||
| Expr2036193 | |||||||||
| Drives_construct | WBCnstr00024237 | ||||||||
| Construct_product | WBCnstr00024237 | ||||||||
| Microarray_results (21) | |||||||||
| Expression_cluster (140) | |||||||||
| Interaction (87) | |||||||||
| Map_info | Positive | Positive_clone | Y102E9 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | III | -0.965119 | |||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
