WormBase Tree Display for Gene: WBGene00008925
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| WBGene00008925 | SMap | S_parent | Sequence | CHROMOSOME_X | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | F17H10.1 | |||||||
| Molecular_name | F17H10.1 | ||||||||
| F17H10.1.1 | |||||||||
| CE03226 | |||||||||
| Other_name | CELE_F17H10.1 | Accession_evidence | NDB | BX284606 | |||||
| Public_name | F17H10.1 | ||||||||
| DB_info | Database | AceView | gene | XN725 | |||||
| WormQTL | gene | WBGene00008925 | |||||||
| WormFlux | gene | WBGene00008925 | |||||||
| NDB | locus_tag | CELE_F17H10.1 | |||||||
| NCBI | gene | 181439 | |||||||
| RefSeq | protein | NM_077776.8 | |||||||
| TREEFAM | TREEFAM_ID | TF319689 | |||||||
| TrEMBL | UniProtAcc | G5ECN2 | |||||||
| UniProt_GCRP | UniProtAcc | G5ECN2 | |||||||
| OMIM | gene | 614725 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:49 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (54) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| Ortholog (34) | |||||||||
| Paralog | WBGene00015486 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
| Structured_description | Automated_description | Enriched in intestine based on RNA-seq studies. Is affected by several genes including daf-16; daf-2; and daf-12 based on microarray; tiling array; RNA-seq; and proteomic studies. Is affected by fifteen chemicals including methylmercuric chloride; rotenone; and D-glucopyranose based on microarray and RNA-seq studies. Human ortholog(s) of this gene implicated in 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome. Is predicted to encode a protein with the following domain: Alpha/Beta hydrolase fold. Is an ortholog of human SERAC1 (serine active site containing 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:0110001 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21061) | ||||
| Molecular_info | Corresponding_CDS | F17H10.1 | |||||||
| Corresponding_transcript | F17H10.1.1 | ||||||||
| Other_sequence (14) | |||||||||
| Associated_feature | WBsf648643 | ||||||||
| WBsf663463 | |||||||||
| WBsf663464 | |||||||||
| WBsf663465 | |||||||||
| WBsf982259 | |||||||||
| WBsf1007518 | |||||||||
| WBsf236535 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00044901 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00114801 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00013478 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00001001 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00031084 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1022569 | ||||||||
| Expr1033886 | |||||||||
| Expr1148872 | |||||||||
| Expr2002699 | |||||||||
| Expr2020914 | |||||||||
| Drives_construct | WBCnstr00032589 | ||||||||
| Construct_product | WBCnstr00032589 | ||||||||
| Microarray_results (21) | |||||||||
| Expression_cluster (144) | |||||||||
| Interaction | WBInteraction000373525 | ||||||||
| WBInteraction000504576 | |||||||||
| Map_info | Positive | Positive_clone | F17H10 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | X | 10.2099 | |||||||
| Reference | WBPaper00029387 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
