WormBase Tree Display for Gene: WBGene00001603
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| WBGene00001603 | Evidence | CGC_data_submission | |||||||
|---|---|---|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | K03H1 | ||||||
| Identity | Version | 1 | |||||||
| Name | CGC_name | gln-2 | |||||||
| Sequence_name | K03H1.1 | ||||||||
| Molecular_name | K03H1.1 | ||||||||
| K03H1.1.1 | |||||||||
| CE00507 | |||||||||
| Other_name | CELE_K03H1.1 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | gln-2 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:25 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | gln | ||||||||
| Allele (79) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (13) | |||||||||
| Ortholog (50) | |||||||||
| Paralog | WBGene00001602 | Caenorhabditis elegans | From_analysis | TreeFam | |||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00001604 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00001606 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
| Inparanoid_8 | |||||||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00014755 | Caenorhabditis elegans | From_analysis | modENCODE_Pseudogenes | ||||||
| WBGene00023306 | Caenorhabditis elegans | From_analysis | modENCODE_Pseudogenes | ||||||
| WBGene00001605 | Caenorhabditis elegans | From_analysis | modENCODE_Pseudogenes | ||||||
| WBGene00001607 | Caenorhabditis elegans | From_analysis | Inparanoid_8 | ||||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Predicted to enable glutamine synthetase activity. Predicted to be involved in glutamine biosynthetic process. Predicted to be located in cytoplasm. Expressed in germ line. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Huntington's disease; congenital glutamine deficiency; and epilepsy (multiple). Is an ortholog of human GLUL (glutamate-ammonia ligase). | Paper_evidence | WBPaper00065943 | |||||
| WBPaper00067038 | |||||||||
| Curator_confirmed | WBPerson324 | ||||||||
| WBPerson37462 | |||||||||
| Inferred_automatically | This description was generated automatically by a script based on data from the WS296 version of WormBase | ||||||||
| Date_last_updated | 20 Mar 2025 00:00:00 | ||||||||
| Disease_info | Potential_model | DOID:0070545 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||
| DOID:10652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:114 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:1070 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:409 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:12858 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:0070544 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:5082 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:3328 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| DOID:5419 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4341) | ||||||
| Molecular_info | Corresponding_CDS | K03H1.1 | |||||||
| Corresponding_transcript | K03H1.1.1 | ||||||||
| Other_sequence (45) | |||||||||
| Associated_feature | WBsf651424 | ||||||||
| WBsf993853 | |||||||||
| WBsf993854 | |||||||||
| WBsf993855 | |||||||||
| WBsf1015701 | |||||||||
| WBsf227392 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00033922 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00087697 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00007016 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049845 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00022543 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00007274 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049843 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00016551 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049844 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr4118 | ||||||||
| Expr1025221 | |||||||||
| Expr1153554 | |||||||||
| Expr2012098 | |||||||||
| Expr2030334 | |||||||||
| Drives_construct | WBCnstr00036831 | ||||||||
| Construct_product | WBCnstr00036831 | ||||||||
| Microarray_results (18) | |||||||||
| Expression_cluster (266) | |||||||||
| Interaction (282) | |||||||||
| Map_info | Map | III | Position | 1.30521 | Error | 0.015066 | |||
| Positive | Positive_clone | K03H1 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00028451 | ||||||||
| WBPaper00031805 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00065140 | |||||||||
| 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 |
