WormBase Tree Display for Gene: WBGene00015266
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| WBGene00015266 | SMap | S_parent | Sequence | BE0003N10 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | BE0003N10.1 | |||||||
| Molecular_name | BE0003N10.1 | ||||||||
| BE0003N10.1.1 | |||||||||
| CE39207 | |||||||||
| Other_name | CELE_BE0003N10.1 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | BE0003N10.1 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:30:55 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (326) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (14) | |||||||||
| Ortholog (37) | |||||||||
| Structured_description | Automated_description | Predicted to enable 3'-5'-RNA exonuclease activity and polyribonucleotide nucleotidyltransferase activity. Predicted to be involved in mitochondrial RNA 3'-end processing and mitochondrial mRNA catabolic process. Predicted to be located in cytosol and mitochondrion. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 70; combined oxidative phosphorylation deficiency 13; and spinocerebellar ataxia type 25. Is an ortholog of human PNPT1 (polyribonucleotide nucleotidyltransferase 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:0050974 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23166) | ||||
| DOID:0110521 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23166) | ||||||
| DOID:0111467 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23166) | ||||||
| Molecular_info | Corresponding_CDS | BE0003N10.1 | |||||||
| Corresponding_CDS_history | BE0003N10.1:wp150 | ||||||||
| Corresponding_transcript | BE0003N10.1.1 | ||||||||
| Other_sequence (34) | |||||||||
| Associated_feature (12) | |||||||||
| Experimental_info | RNAi_result | WBRNAi00039217 | Inferred_automatically | RNAi_primary | |||||
| Expr_pattern | Expr1022496 | ||||||||
| Expr1036539 | |||||||||
| Expr1143360 | |||||||||
| Expr2000254 | |||||||||
| Expr2018474 | |||||||||
| Microarray_results (18) | |||||||||
| Expression_cluster (86) | |||||||||
| Interaction (77) | |||||||||
| Map_info | Positive | Positive_clone | BE0003N10 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | III | -24.7829 | |||||||
| Reference | WBPaper00035488 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
