WormBase Tree Display for Gene: WBGene00011672
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| WBGene00011672 | SMap | S_parent | Sequence | T10B9 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | cyp-13A5 | |||||||
| Sequence_name | T10B9.2 | ||||||||
| Molecular_name | T10B9.2 | ||||||||
| T10B9.2.1 | |||||||||
| CE01656 | |||||||||
| Other_name | CELE_T10B9.2 | Accession_evidence | NDB | BX284602 | |||||
| Public_name | cyp-13A5 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 21 Sep 2004 09:38:16 | WBPerson1971 | Name_change | CGC_name | cyp-13A5 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | cyp | ||||||||
| Allele (36) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00079947 | ||||||||
| 00079948 | |||||||||
| 00079949 | |||||||||
| 00118899 | |||||||||
| 00118900 | |||||||||
| 00118901 | |||||||||
| 00118902 | |||||||||
| Ortholog (64) | |||||||||
| Paralog (12) | |||||||||
| Structured_description | Concise_description | cyp-13A5 encodes one of ~80 C. elegans cytochrome P450s: membrane-associated, heme-containing NADPH-dependent monooxygenases that catalyze the oxidative metabolism of a variety of exogenous compounds and endogenous substrates; loss of cyp-13A5 activity in large-scale RNAi screens results in uncoordinated locomotion, decreased and/or slow growth, and cadmium hypersensitivity. | Paper_evidence | WBPaper00005654 | |||||
| WBPaper00006395 | |||||||||
| WBPaper00030811 | |||||||||
| Curator_confirmed | WBPerson1843 | ||||||||
| Date_last_updated | 20 Nov 2008 00:00:00 | ||||||||
| Automated_description | Predicted to enable heme binding activity; iron ion binding activity; and oxidoreductase activity. Human ortholog(s) of this gene implicated in several diseases, including Ghosal hematodiaphyseal syndrome; familial Mediterranean fever; and leukemia (multiple). Is an ortholog of several human genes including CYP3A4 (cytochrome P450 family 3 subfamily A member 4); CYP3A5 (cytochrome P450 family 3 subfamily A member 5); and CYP3A7 (cytochrome P450 family 3 subfamily A member 7). | 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:8552 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2638) | ||||
| DOID:3526 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11609) | ||||||
| DOID:2987 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2637) | ||||||
| DOID:9952 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2638) | ||||||
| DOID:0112251 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11609) | ||||||
| DOID:0080630 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2638) | ||||||
| DOID:10825 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2638) | ||||||
| DOID:1612 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2637) | ||||||
| Molecular_info | Corresponding_CDS | T10B9.2 | |||||||
| Corresponding_transcript | T10B9.2.1 | ||||||||
| Other_sequence | JI174138.1 | ||||||||
| Oden_isotig14710 | |||||||||
| Acan_isotig21796 | |||||||||
| Associated_feature | WBsf223709 | ||||||||
| WBsf223710 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00018525 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00070152 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00053015 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00035421 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00092623 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1156616 | ||||||||
| Expr2010685 | |||||||||
| Expr2028924 | |||||||||
| Drives_construct | WBCnstr00030481 | ||||||||
| Construct_product | WBCnstr00030481 | ||||||||
| Microarray_results (14) | |||||||||
| Expression_cluster (327) | |||||||||
| Interaction (36) | |||||||||
| Map_info | Map | II | Position | 1.7164 | Error | 0.000227 | |||
| Positive | Positive_clone | T10B9 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00037579 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00042257 | |||||||||
| WBPaper00055090 | |||||||||
| WBPaper00064073 | |||||||||
| WBPaper00064598 | |||||||||
| WBPaper00065331 | |||||||||
| 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 |
