WormBase Tree Display for Gene: WBGene00008624
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| WBGene00008624 | SMap | S_parent | Sequence | F09E8 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | crld-1 | Person_evidence | WBPerson61 | |||||
| Sequence_name | F09E8.2 | ||||||||
| Molecular_name | F09E8.2a | ||||||||
| F09E8.2a.1 | |||||||||
| CE05579 | |||||||||
| F09E8.2b | |||||||||
| CE41378 | |||||||||
| F09E8.2a.2 | |||||||||
| F09E8.2b.1 | |||||||||
| F09E8.2b.2 | |||||||||
| Other_name | CELE_F09E8.2 | Accession_evidence | NDB | BX284604 | |||||
| Public_name | crld-1 | ||||||||
| DB_info | Database (13) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:49 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 11 Jun 2018 11:44:56 | WBPerson1983 | Name_change | CGC_name | crld | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | crld | ||||||||
| Allele (54) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00064145 | ||||||||
| 00064146 | |||||||||
| 00064147 | |||||||||
| 00064148 | |||||||||
| 00064149 | |||||||||
| 00064150 | |||||||||
| 00105626 | |||||||||
| 00116504 | |||||||||
| Ortholog (39) | |||||||||
| Paralog (16) | |||||||||
| Structured_description | Automated_description | Predicted to enable calcium ion binding activity and protein disulfide isomerase activity. Involved in IRE1-mediated unfolded protein response. Predicted to be located in endoplasmic reticulum lumen and endoplasmic reticulum membrane. Expressed in several structures, including body wall musculature; gonad; hypodermis; intestine; and pharynx. Human ortholog(s) of this gene implicated in atrioventricular septal defect. Is an ortholog of human CRELD1 (cysteine rich with EGF like domains 1) and CRELD2 (cysteine rich with EGF like domains 2). | 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:0050651 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14630) | ||||
| DOID:1681 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:14630) | ||||||
| Molecular_info | Corresponding_CDS | F09E8.2a | |||||||
| F09E8.2b | |||||||||
| Corresponding_transcript | F09E8.2a.1 | ||||||||
| F09E8.2a.2 | |||||||||
| F09E8.2b.1 | |||||||||
| F09E8.2b.2 | |||||||||
| Other_sequence (35) | |||||||||
| Associated_feature | WBsf652326 | ||||||||
| WBsf668450 | |||||||||
| WBsf231090 | |||||||||
| WBsf231091 | |||||||||
| WBsf231092 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00044135 | Inferred_automatically | RNAi_primary | |||||
| Expr_pattern | Expr13991 | ||||||||
| Expr13992 | |||||||||
| Expr1012319 | |||||||||
| Expr1033757 | |||||||||
| Expr1148103 | |||||||||
| Expr2002352 | |||||||||
| Expr2020570 | |||||||||
| Drives_construct | WBCnstr00032821 | ||||||||
| Construct_product | WBCnstr00032821 | ||||||||
| Microarray_results (23) | |||||||||
| Expression_cluster (100) | |||||||||
| Interaction | WBInteraction000232077 | ||||||||
| WBInteraction000287415 | |||||||||
| WBInteraction000297873 | |||||||||
| WBInteraction000325674 | |||||||||
| WBInteraction000337609 | |||||||||
| WBInteraction000341764 | |||||||||
| WBInteraction000425202 | |||||||||
| WBInteraction000445983 | |||||||||
| WBInteraction000559802 | |||||||||
| Map_info | Map | IV | Position | 8.2248 | |||||
| Positive | Positive_clone | F09E8 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00026830 | ||||||||
| 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 |
