WormBase Tree Display for Gene: WBGene00011128
expand all nodes | collapse all nodes | view schema
| WBGene00011128 | SMap | S_parent | Sequence | R07H5 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | adk-1 | Person_evidence | WBPerson10610 | |||||
| Sequence_name | R07H5.8 | ||||||||
| Molecular_name | R07H5.8 | ||||||||
| R07H5.8.1 | |||||||||
| CE12564 | |||||||||
| Other_name | CELE_R07H5.8 | Accession_evidence | NDB | BX284604 | |||||
| Public_name | adk-1 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 20 May 2019 14:10:26 | WBPerson1983 | Name_change | CGC_name | adk-1 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | adk | ||||||||
| Allele (23) | |||||||||
| Strain | WBStrain00002930 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (24) | |||||||||
| Ortholog (41) | |||||||||
| Paralog | WBGene00008548 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
| WBGene00013720 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| WBGene00020765 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| Structured_description | Automated_description | Predicted to enable adenosine kinase activity. Predicted to be involved in purine nucleobase metabolic process. Predicted to be located in cytosol and nucleus. Human ortholog(s) of this gene implicated in hypermethioninemia due to adenosine kinase deficiency and temporal lobe epilepsy. Is an ortholog of human ADK (adenosine kinase). | 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:0111038 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:257) | ||||
| DOID:3328 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:257) | ||||||
| Molecular_info | Corresponding_CDS | R07H5.8 | |||||||
| Corresponding_transcript | R07H5.8.1 | ||||||||
| Other_sequence (63) | |||||||||
| Associated_feature | WBsf652198 | ||||||||
| WBsf655529 | |||||||||
| WBsf997793 | |||||||||
| WBsf230843 | |||||||||
| Experimental_info | RNAi_result (18) | ||||||||
| Expr_pattern | Chronogram1261 | ||||||||
| Expr6482 | |||||||||
| Expr1021627 | |||||||||
| Expr1034894 | |||||||||
| Expr1155192 | |||||||||
| Expr2005476 | |||||||||
| Expr2023697 | |||||||||
| Drives_construct | WBCnstr00003442 | ||||||||
| WBCnstr00030909 | |||||||||
| Construct_product | WBCnstr00030909 | ||||||||
| Microarray_results | SMD_R07H5.8 | ||||||||
| SMD_R07H5.9 | |||||||||
| 189371_s_at | |||||||||
| A_12_P116260 | |||||||||
| Aff_R07H5.8 | |||||||||
| GPL13394_WBGene00011128 | |||||||||
| GPL13914_R07H5.8 | |||||||||
| GPL14144_R07H5.8_311-370_0.884_28_C | |||||||||
| GPL14144_R07H5.8_421-480_0.910_12_B | |||||||||
| GPL14144_R07H5.8_936-995_0.959_1_A | |||||||||
| GPL19516_CGZ0031369 | |||||||||
| GPL21109_R07H5.8 | |||||||||
| GPL3518_CE12564 | |||||||||
| GPL8304_CE_WBGene00011128_A | |||||||||
| GPL8673_R07H5_8P00323 | |||||||||
| GPL8673_R07H5_8P00501 | |||||||||
| GPL8673_R07H5_8P00682 | |||||||||
| GPL9450_R07H5.8 | |||||||||
| cea2.c.30585 | |||||||||
| Expression_cluster (163) | |||||||||
| Interaction (193) | |||||||||
| Map_info | Map | IV | Position | 4.92533 | |||||
| Positive | Positive_clone | R07H5 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00044448 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00065026 | |||||||||
| 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 |
