WormBase Tree Display for Gene: WBGene00011043
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| WBGene00011043 | SMap | S_parent | Sequence | R05H10 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | rbm-28 | Paper_evidence | WBPaper00037676 | |||||
| Person_evidence | WBPerson472 | ||||||||
| Sequence_name | R05H10.2 | ||||||||
| Molecular_name | R05H10.2 | ||||||||
| R05H10.2.1 | |||||||||
| CE31214 | |||||||||
| Other_name | CELE_R05H10.2 | Accession_evidence | NDB | BX284602 | |||||
| Public_name | rbm-28 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 19 Oct 2010 16:33:34 | WBPerson2970 | Name_change | CGC_name | rbm-28 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | rbm | ||||||||
| Allele (180) | |||||||||
| Strain | WBStrain00003050 | ||||||||
| WBStrain00051401 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00037697 | ||||||||
| 00037698 | |||||||||
| 00037699 | |||||||||
| 00118341 | |||||||||
| 00118342 | |||||||||
| Contained_in_operon | CEOP2652 | ||||||||
| Ortholog (39) | |||||||||
| Paralog (14) | |||||||||
| Structured_description | Automated_description | Predicted to enable RNA binding activity. Predicted to be located in nucleolus. Expressed in head and tail. Used to study alopecia, neurologic defects, and endocrinopathy syndrome. Human ortholog(s) of this gene implicated in alopecia, neurologic defects, and endocrinopathy syndrome. Is an ortholog of human RBM28 (RNA binding motif protein 28). | 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 | Experimental_model | DOID:0112244 | Homo sapiens | Paper_evidence | WBPaper00037676 | ||||
| Curator_confirmed | WBPerson324 | ||||||||
| Date_last_updated | 23 Feb 2021 00:00:00 | ||||||||
| Potential_model | DOID:0112244 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21863) | |||||
| Models_disease_in_annotation | WBDOannot00000868 | ||||||||
| Molecular_info | Corresponding_CDS | R05H10.2 | |||||||
| Corresponding_CDS_history | R05H10.2:wp80 | ||||||||
| Corresponding_transcript | R05H10.2.1 | ||||||||
| Other_sequence (44) | |||||||||
| Associated_feature | WBsf644875 | ||||||||
| WBsf658441 | |||||||||
| WBsf658442 | |||||||||
| WBsf658443 | |||||||||
| WBsf658444 | |||||||||
| WBsf658445 | |||||||||
| WBsf222517 | |||||||||
| Experimental_info | RNAi_result (22) | ||||||||
| Expr_pattern | Chronogram1241 | ||||||||
| Expr6466 | |||||||||
| Expr1022249 | |||||||||
| Expr1034844 | |||||||||
| Expr1155029 | |||||||||
| Expr2015272 | |||||||||
| Expr2033506 | |||||||||
| Drives_construct | WBCnstr00003547 | ||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (92) | |||||||||
| Interaction (288) | |||||||||
| Map_info | Map | II | Position | 23.6571 | Error | 0.015992 | |||
| Positive | Positive_clone | R05H10 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00029208 | ||||||||
| WBPaper00037676 | |||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| 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 |
