WormBase Tree Display for Gene: WBGene00010769
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| WBGene00010769 | SMap | S_parent | Sequence | K11D2 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | asah-1 | |||||||
| Sequence_name | K11D2.2 | ||||||||
| Molecular_name | K11D2.2 | ||||||||
| K11D2.2.1 | |||||||||
| CE12120 | |||||||||
| Other_name | dod-7 | CGC_data_submission | |||||||
| CELE_K11D2.2 | Accession_evidence | NDB | BX284601 | ||||||
| Public_name | asah-1 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:51 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 25 Aug 2004 14:17:26 | WBPerson1971 | Name_change | CGC_name | asah-1 | ||||
| Other_name | dod-7 | ||||||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | asah | ||||||||
| Allele (54) | |||||||||
| Strain | WBStrain00033927 | ||||||||
| WBStrain00055428 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (15) | |||||||||
| Ortholog (39) | |||||||||
| Paralog | WBGene00009192 | Caenorhabditis elegans | From_analysis | Panther | |||||
| WormBase-Compara | |||||||||
| WBGene00021917 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Predicted to enable N-acylsphingosine amidohydrolase activity. Predicted to be involved in fatty acid metabolic process and sphingolipid metabolic process. Predicted to be located in extracellular region and lysosome. Human ortholog(s) of this gene implicated in Farber lipogranulomatosis; sphingolipidosis; and spinal muscular atrophy with progressive myoclonic epilepsy. Is an ortholog of human ASAH1 (N-acylsphingosine amidohydrolase 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:0111527 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:735) | ||||
| DOID:1927 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:735) | ||||||
| DOID:0050464 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:735) | ||||||
| Molecular_info | Corresponding_CDS | K11D2.2 | |||||||
| Corresponding_transcript | K11D2.2.1 | ||||||||
| Other_sequence (52) | |||||||||
| Associated_feature | WBsf643764 | ||||||||
| WBsf985584 | |||||||||
| WBsf218603 | |||||||||
| WBsf218604 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00034283 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00063174 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00090564 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00001097 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00003984 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00050596 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern (12) | |||||||||
| Drives_construct | WBCnstr00001079 | ||||||||
| WBCnstr00002691 | |||||||||
| WBCnstr00004394 | |||||||||
| WBCnstr00011665 | |||||||||
| WBCnstr00043068 | |||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (315) | |||||||||
| Interaction (25) | |||||||||
| Map_info | Map | I | Position | 13.2437 | Error | 0.0148 | |||
| Positive | Positive_clone | K11D2 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Mapping_data | Multi_point | 5396 | |||||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00005976 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00041771 | |||||||||
| WBPaper00042257 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00065215 | |||||||||
| WBPaper00065849 | |||||||||
| 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 |
