WormBase Tree Display for Gene: WBGene00004383
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| WBGene00004383 | Evidence | Accession_evidence | EMBL | AF181619 | |||||
|---|---|---|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | T13H5 | ||||||
| Identity | Version | 1 | |||||||
| Name | CGC_name | rnh-2 | |||||||
| Sequence_name | T13H5.7 | ||||||||
| Molecular_name | T13H5.7 | ||||||||
| T13H5.7.1 | |||||||||
| CE28960 | |||||||||
| Other_name | rnh2 | Accession_evidence | EMBL | AF181619 | |||||
| CELE_T13H5.7 | Accession_evidence | NDB | BX284602 | ||||||
| Public_name | rnh-2 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:35 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | rnh | ||||||||
| Allele (20) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (14) | |||||||||
| Contained_in_operon | CEOP2356 | ||||||||
| Ortholog (38) | |||||||||
| Structured_description | Concise_description | rnh-2 encodes the C. elegans ortholog of the large subunit of ribonuclease H2 (RNase H2). | Paper_evidence | WBPaper00005577 | |||||
| Curator_confirmed | WBPerson1843 | ||||||||
| Date_last_updated | 02 Aug 2007 00:00:00 | ||||||||
| Automated_description | Predicted to enable RNA-DNA hybrid ribonuclease activity. Predicted to be involved in DNA replication, removal of RNA primer and mismatch repair. Predicted to be part of ribonuclease H2 complex. Human ortholog(s) of this gene implicated in Aicardi-Goutieres syndrome. Is an ortholog of human RNASEH2A (ribonuclease H2 subunit A). | 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:0050629 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:18518) | ||||
| Molecular_info | Corresponding_CDS | T13H5.7 | |||||||
| Corresponding_transcript | T13H5.7.1 | ||||||||
| Other_sequence (32) | |||||||||
| Associated_feature | WBsf644475 | ||||||||
| WBsf221759 | |||||||||
| WBsf221760 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00027913 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00053302 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00053301 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1012567 | ||||||||
| Expr1032194 | |||||||||
| Expr1156887 | |||||||||
| Expr2015389 | |||||||||
| Expr2033623 | |||||||||
| Drives_construct | WBCnstr00035522 | ||||||||
| Construct_product | WBCnstr00035522 | ||||||||
| Microarray_results (18) | |||||||||
| Expression_cluster (125) | |||||||||
| Interaction (55) | |||||||||
| Map_info | Map | II | Position | 0.814627 | Error | 0.000208 | |||
| Positive | Positive_clone | T13H5 | Inferred_automatically | From CDS info | |||||
| From sequence, transcript, pseudogene data | |||||||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00005577 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00064312 | |||||||||
| 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 |
