WormBase Tree Display for Gene: WBGene00001055
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| WBGene00001055 | Evidence | Person_evidence | WBPerson2549 | ||||||
|---|---|---|---|---|---|---|---|---|---|
| WBPerson6733 | |||||||||
| SMap | S_parent | Sequence | C27C12 | ||||||
| Identity | Version | 1 | |||||||
| Name | CGC_name | dpf-2 | |||||||
| Sequence_name | C27C12.7 | ||||||||
| Molecular_name | C27C12.7 | ||||||||
| C27C12.7.1 | |||||||||
| CE05324 | |||||||||
| Other_name | CELE_C27C12.7 | Accession_evidence | NDB | BX284606 | |||||
| Public_name | dpf-2 | ||||||||
| DB_info | Database (11) | ||||||||
| 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 | dpf | ||||||||
| Allele (111) | |||||||||
| Strain | WBStrain00003293 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (13) | |||||||||
| Ortholog (37) | |||||||||
| Paralog | WBGene00001054 | Caenorhabditis elegans | From_analysis | TreeFam | |||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00001056 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00001057 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| WBGene00001058 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| WBGene00001059 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
| Structured_description | Automated_description | Predicted to enable dipeptidyl-peptidase activity. Predicted to be involved in proteolysis. Predicted to be located in plasma membrane. Expressed in head. Human ortholog(s) of this gene implicated in Middle East respiratory syndrome; squamous cell carcinoma (multiple); and type 2 diabetes mellitus. Is an ortholog of human FAP (fibroblast activation protein alpha). | 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:3908 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3590) | ||||
| DOID:3748 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3009,HGNC:3590) | ||||||
| DOID:0080642 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3009) | ||||||
| DOID:9352 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3009) | ||||||
| DOID:3907 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3590) | ||||||
| Molecular_info | Corresponding_CDS | C27C12.7 | |||||||
| Corresponding_transcript | C27C12.7.1 | ||||||||
| Other_sequence | Acan_isotig10074 | ||||||||
| JI165532.1 | |||||||||
| Dviv_isotig24688 | |||||||||
| Oden_isotig19299 | |||||||||
| Associated_feature | WBsf663597 | ||||||||
| WBsf718775 | |||||||||
| WBsf1008017 | |||||||||
| WBsf1008018 | |||||||||
| WBsf1008019 | |||||||||
| WBsf1024470 | |||||||||
| WBsf236722 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00041330 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00041329 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00088996 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00011253 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00029266 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr5353 | ||||||||
| Expr1013442 | |||||||||
| Expr1030665 | |||||||||
| Expr1145373 | |||||||||
| Expr2011040 | |||||||||
| Expr2029277 | |||||||||
| Drives_construct | WBCnstr00003764 | ||||||||
| WBCnstr00037115 | |||||||||
| Construct_product | WBCnstr00037115 | ||||||||
| Microarray_results (19) | |||||||||
| Expression_cluster (168) | |||||||||
| Interaction (11) | |||||||||
| Map_info | Map | X | Position | 21.4249 | Error | 0.006483 | |||
| Positive | Positive_clone | C27C12 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00010074 | ||||||||
| WBPaper00019587 | |||||||||
| WBPaper00025499 | |||||||||
| WBPaper00028704 | |||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| 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 |
