WormBase Tree Display for Gene: WBGene00000972
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| WBGene00000972 | SMap | S_parent | Sequence | K10H10 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | dhs-8 | Person_evidence | WBPerson651 | |||||
| Sequence_name | K10H10.3 | ||||||||
| Molecular_name | K10H10.3a | ||||||||
| K10H10.3a.1 | |||||||||
| CE16253 | |||||||||
| K10H10.3c | |||||||||
| CE49107 | |||||||||
| K10H10.3d | |||||||||
| CE48898 | |||||||||
| K10H10.3b | |||||||||
| K10H10.3c.1 | |||||||||
| K10H10.3d.1 | |||||||||
| Other_name | CELE_K10H10.3 | Accession_evidence | NDB | BX284602 | |||||
| Public_name | dhs-8 | ||||||||
| DB_info | Database (12) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:22 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | dhs | ||||||||
| Allele (38) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00034972 | ||||||||
| Ortholog (21) | |||||||||
| Paralog (11) | |||||||||
| Structured_description | Automated_description | Predicted to enable oxidoreductase activity. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 12; developmental and epileptic encephalopathy 28; and esophagus squamous cell carcinoma. Is an ortholog of human WWOX (WW domain containing oxidoreductase). | 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:3748 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12799) | ||||
| DOID:5041 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12799) | ||||||
| DOID:0080452 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12799) | ||||||
| DOID:0080060 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12799) | ||||||
| DOID:1749 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:12799) | ||||||
| Molecular_info | Corresponding_CDS | K10H10.3a | |||||||
| K10H10.3c | |||||||||
| K10H10.3d | |||||||||
| Corresponding_transcript | K10H10.3b | ||||||||
| K10H10.3a.1 | |||||||||
| K10H10.3c.1 | |||||||||
| K10H10.3d.1 | |||||||||
| Associated_feature | WBsf644859 | ||||||||
| WBsf657184 | |||||||||
| WBsf222470 | |||||||||
| WBsf222471 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00022401 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00034272 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00050567 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1024651 | ||||||||
| Expr1030606 | |||||||||
| Expr1154276 | |||||||||
| Expr2010922 | |||||||||
| Expr2029161 | |||||||||
| Drives_construct | WBCnstr00037167 | ||||||||
| Construct_product | WBCnstr00037167 | ||||||||
| Microarray_results (24) | |||||||||
| Expression_cluster (189) | |||||||||
| Interaction | WBInteraction000047019 | ||||||||
| WBInteraction000047023 | |||||||||
| WBInteraction000047024 | |||||||||
| WBInteraction000305809 | |||||||||
| WBInteraction000309034 | |||||||||
| WBInteraction000425512 | |||||||||
| WBInteraction000444353 | |||||||||
| WBInteraction000505030 | |||||||||
| Map_info | Map | II | Position | 23.0371 | Error | 0.002143 | |||
| Positive | Positive_clone | K10H10 | Inferred_automatically | From CDS info | |||||
| From sequence, transcript, pseudogene data | |||||||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00042257 | |||||||||
| WBPaper00055090 | |||||||||
| Picture | WBPicture0000013093 | ||||||||
| 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 |
