WormBase Tree Display for Gene: WBGene00010664
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WBGene00010664 | SMap | S_parent | Sequence | K08E3 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | dbn-1 | Person_evidence | WBPerson17543 | |||||
Sequence_name | K08E3.4 | ||||||||
Molecular_name | K08E3.4 | ||||||||
K08E3.4.1 | |||||||||
CE18868 | |||||||||
Other_name | CELE_K08E3.4 | Accession_evidence | NDB | BX284603 | |||||
Public_name | dbn-1 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:51 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 11 Jul 2014 14:45:03 | WBPerson2970 | Name_change | CGC_name | abn-1 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | dbn | ||||||||
Allele (66) | |||||||||
Strain | WBStrain00031713 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (16) | |||||||||
Contained_in_operon | CEOP3829 | ||||||||
Ortholog (44) | |||||||||
Structured_description | Automated_description | Predicted to enable actin filament binding activity. Predicted to be involved in cellular component organization and positive regulation of neurogenesis. Predicted to be located in several cellular components, including actin cytoskeleton; plasma membrane bounded cell projection; and postsynapse. Human ortholog(s) of this gene implicated in Alzheimer's disease; Down syndrome; and cognitive disorder. Is an ortholog of human DBNL (drebrin 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:10652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2695) | ||||
DOID:14250 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2695) | ||||||
DOID:1561 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2695) | ||||||
Molecular_info | Corresponding_CDS | K08E3.4 | |||||||
Corresponding_transcript | K08E3.4.1 | ||||||||
Other_sequence (33) | |||||||||
Associated_feature | WBsf981657 | ||||||||
WBsf995014 | |||||||||
WBsf995015 | |||||||||
WBsf227791 | |||||||||
WBsf227792 | |||||||||
WBsf227793 | |||||||||
Experimental_info | RNAi_result | WBRNAi00080543 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00117317 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00114664 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00117316 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00050284 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00016807 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00117315 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00077333 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00117318 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00034133 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr14431 | ||||||||
Expr1016575 | |||||||||
Expr1034662 | |||||||||
Expr1153986 | |||||||||
Expr2010798 | |||||||||
Expr2029035 | |||||||||
Drives_construct | WBCnstr00031242 | ||||||||
Construct_product | WBCnstr00031242 | ||||||||
WBCnstr00040856 | |||||||||
Antibody | WBAntibody00002644 | ||||||||
Microarray_results (19) | |||||||||
Expression_cluster (105) | |||||||||
Interaction (107) | |||||||||
Map_info | Map | III | Position | 21.4952 | |||||
Positive | Positive_clone | K08E3 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference | WBPaper00024200 | ||||||||
WBPaper00031546 | |||||||||
WBPaper00038491 | |||||||||
WBPaper00046990 | |||||||||
WBPaper00049824 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00056797 | |||||||||
WBPaper00064659 | |||||||||
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 |