WormBase Tree Display for Gene: WBGene00017827
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| WBGene00017827 | SMap | S_parent | Sequence | F26F4 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | F26F4.5 | |||||||
| Molecular_name | F26F4.5 | ||||||||
| F26F4.5.1 | |||||||||
| CE29289 | |||||||||
| F26F4.5.2 | |||||||||
| Other_name | CELE_F26F4.5 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | F26F4.5 | ||||||||
| DB_info | Database | AceView | gene | 3F978 | |||||
| WormQTL | gene | WBGene00017827 | |||||||
| WormFlux | gene | WBGene00017827 | |||||||
| NDB | locus_tag | CELE_F26F4.5 | |||||||
| NCBI | gene | 175653 | |||||||
| RefSeq | protein | NM_065623.7 | |||||||
| TrEMBL | UniProtAcc | Q19816 | |||||||
| UniProt_GCRP | UniProtAcc | Q19816 | |||||||
| OMIM | gene | 614140 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:30:59 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (23) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00065928 | ||||||||
| 00065929 | |||||||||
| 00065930 | |||||||||
| Contained_in_operon | CEOP3232 | ||||||||
| Ortholog (27) | |||||||||
| Structured_description | Automated_description | Predicted to be involved in actin cytoskeleton organization. Predicted to be located in microtubule organizing center. Predicted to be part of filamentous actin. Human ortholog(s) of this gene implicated in Teebi hypertelorism syndrome 1 and oblique facial clefting 1. Is an ortholog of human SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1 like). | 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:0080698 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:29022) | ||||
| DOID:0111706 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:29022) | ||||||
| Molecular_info | Corresponding_CDS | F26F4.5 | |||||||
| Corresponding_transcript | F26F4.5.1 | ||||||||
| F26F4.5.2 | |||||||||
| Other_sequence | CJC11164_1 | ||||||||
| CBC04044_1 | |||||||||
| CRC06540_1 | |||||||||
| CR03497 | |||||||||
| CBC16256_1 | |||||||||
| Associated_feature | WBsf666426 | ||||||||
| WBsf666832 | |||||||||
| WBsf992239 | |||||||||
| WBsf226595 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00007752 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00005256 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00001351 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00045678 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00013965 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1012173 | ||||||||
| Expr1037660 | |||||||||
| Expr1149589 | |||||||||
| Expr2003036 | |||||||||
| Expr2021250 | |||||||||
| Drives_construct | WBCnstr00026983 | ||||||||
| Construct_product | WBCnstr00026983 | ||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (106) | |||||||||
| Interaction (26) | |||||||||
| Map_info | Positive | Positive_clone | F26F4 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | III | -2.40778 | |||||||
| Reference | WBPaper00060275 | ||||||||
| Method | Gene |
