WormBase Tree Display for Gene: WBGene00008136
expand all nodes | collapse all nodes | view schema
| WBGene00008136 | SMap | S_parent | Sequence | C47D12 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | C47D12.2 | |||||||
| Molecular_name | C47D12.2 | ||||||||
| C47D12.2.1 | |||||||||
| CE20567 | |||||||||
| Other_name | CELE_C47D12.2 | Accession_evidence | NDB | BX284602 | |||||
| Public_name | C47D12.2 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:48 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (56) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00061910 | ||||||||
| 00061911 | |||||||||
| 00061912 | |||||||||
| Ortholog (37) | |||||||||
| Structured_description | Concise_description | C47D12.2 encodes an ortholog of human FLJ20071/FLJ90130 (dymeclin, OMIM:607461, mutated in Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia). | Paper_evidence | WBPaper00005654 | |||||
| WBPaper00013114 | |||||||||
| WBPaper00013195 | |||||||||
| WBPaper00013213 | |||||||||
| Curator_confirmed | WBPerson1843 | ||||||||
| WBPerson567 | |||||||||
| Date_last_updated | 30 Jul 2012 00:00:00 | ||||||||
| Automated_description | Predicted to be involved in Golgi organization. Located in endoplasmic reticulum. Human ortholog(s) of this gene implicated in Smith-McCort dysplasia 1. Is an ortholog of human DYM (dymeclin). | 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:0081270 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21317) | ||||
| DOID:2256 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21317) | ||||||
| DOID:0111167 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:21317) | ||||||
| Molecular_info | Corresponding_CDS | C47D12.2 | |||||||
| Corresponding_transcript | C47D12.2.1 | ||||||||
| Other_sequence (46) | |||||||||
| Associated_feature | WBsf644708 | ||||||||
| WBsf222175 | |||||||||
| Experimental_info | RNAi_result (19) | ||||||||
| Expr_pattern | Expr7768 | ||||||||
| Expr9541 | |||||||||
| Expr1014435 | |||||||||
| Expr1033532 | |||||||||
| Expr1146650 | |||||||||
| Expr2001707 | |||||||||
| Expr2019934 | |||||||||
| Drives_construct | WBCnstr00012913 | ||||||||
| WBCnstr00033215 | |||||||||
| Construct_product | WBCnstr00014106 | ||||||||
| WBCnstr00033215 | |||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (88) | |||||||||
| Interaction (115) | |||||||||
| Map_info | Positive | Positive_clone | C47D12 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | II | 3.9301 | |||||||
| Reference | WBPaper00038444 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
