WormBase Tree Display for Gene: WBGene00009002
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| WBGene00009002 | SMap | S_parent | Sequence | F21C3 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 3 | |||||||
| Name | CGC_name | hint-1 | |||||||
| Sequence_name | F21C3.3 | ||||||||
| Molecular_name | F21C3.3 | ||||||||
| F21C3.3.1 | |||||||||
| CE05678 | |||||||||
| F21C3.3.2 | |||||||||
| Other_name | tag-202 | Person_evidence | WBPerson201 | ||||||
| CELE_F21C3.3 | Accession_evidence | NDB | BX284601 | ||||||
| Public_name | hint-1 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:49 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 23 Dec 2004 11:12:00 | WBPerson2970 | Name_change | CGC_name | tag-202 | ||||
| 3 | 27 Mar 2008 14:49:40 | WBPerson2970 | Name_change | CGC_name | hint-1 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | hint | ||||||||
| Allele (18) | |||||||||
| Strain | WBStrain00035947 | ||||||||
| WBStrain00055400 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00048121 | ||||||||
| 00048122 | |||||||||
| 00048123 | |||||||||
| 00048124 | |||||||||
| 00116800 | |||||||||
| Contained_in_operon | CEOP1384 | ||||||||
| Ortholog (37) | |||||||||
| Structured_description | Automated_description | Predicted to enable hydrolase activity. Predicted to be involved in purine ribonucleotide catabolic process. Predicted to be located in cytoplasm and nucleus. Human ortholog(s) of this gene implicated in Gamstorp-Wohlfart syndrome. Is an ortholog of human HINT1 (histidine triad nucleotide binding protein 1). | 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:0050526 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4912) | ||||
| Molecular_info | Corresponding_CDS | F21C3.3 | |||||||
| Corresponding_transcript | F21C3.3.1 | ||||||||
| F21C3.3.2 | |||||||||
| Other_sequence (56) | |||||||||
| Associated_feature | WBsf219727 | ||||||||
| WBsf219728 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00045181 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00003411 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00092968 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00076321 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00031208 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00116531 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1027154 | ||||||||
| Expr1033919 | |||||||||
| Expr1149121 | |||||||||
| Expr2012434 | |||||||||
| Expr2030670 | |||||||||
| Drives_construct | WBCnstr00037860 | ||||||||
| Construct_product | WBCnstr00037860 | ||||||||
| Microarray_results (18) | |||||||||
| Expression_cluster (88) | |||||||||
| Interaction (57) | |||||||||
| Map_info | Map | I | Position | 1.87133 | Error | 0.000432 | |||
| Positive | Positive_clone | F21C3 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Mapping_data | Multi_point | 4953 | |||||||
| 5056 | |||||||||
| 5087 | |||||||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00055090 | |||||||||
| WBPaper00064339 | |||||||||
| 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 |
