WormBase Tree Display for Gene: WBGene00020924
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WBGene00020924 | SMap | S_parent | Sequence | W02B3 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | Sequence_name | W02B3.4 | |||||||
Molecular_name | W02B3.4 | ||||||||
W02B3.4.1 | |||||||||
CE34600 | |||||||||
Other_name | CELE_W02B3.4 | Accession_evidence | NDB | BX284603 | |||||
Public_name | W02B3.4 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:31:03 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (87) | |||||||||
Strain | WBStrain00003334 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00053424 | ||||||||
00053425 | |||||||||
00053426 | |||||||||
Ortholog (36) | |||||||||
Paralog | WBGene00011554 | Caenorhabditis elegans | From_analysis | TreeFam | |||||
Inparanoid_8 | |||||||||
Panther | |||||||||
WormBase-Compara | |||||||||
WBGene00017877 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Inparanoid_8 | |||||||||
WBGene00020307 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Inparanoid_8 | |||||||||
Panther | |||||||||
WormBase-Compara | |||||||||
WBGene00020308 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
WBGene00020309 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Inparanoid_8 | |||||||||
WBGene00021249 | Caenorhabditis elegans | From_analysis | TreeFam | ||||||
Inparanoid_8 | |||||||||
Panther | |||||||||
WormBase-Compara | |||||||||
WBGene00020927 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00045475 | Caenorhabditis elegans | From_analysis | Panther | ||||||
Structured_description | Automated_description | Predicted to be involved in protein glycosylation. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in Fukuyama congenital muscular dystrophy; Walker-Warburg syndrome; autosomal recessive limb-girdle muscular dystrophy type 2L; autosomal recessive limb-girdle muscular dystrophy type 2M; dilated cardiomyopathy (multiple); and muscular dystrophy-dystroglycanopathy type B4. Is an ortholog of human FKTN (fukutin). | 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 (8) | ||||||||
Molecular_info | Corresponding_CDS | W02B3.4 | |||||||
Corresponding_CDS_history | W02B3.4:wp102 | ||||||||
Corresponding_transcript | W02B3.4.1 | ||||||||
Other_sequence | Acan_isotig16043 | ||||||||
Associated_feature | WBsf226121 | ||||||||
Experimental_info | RNAi_result | WBRNAi00036177 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00054567 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00006634 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern (6) | |||||||||
Drives_construct | WBCnstr00003805 | ||||||||
WBCnstr00024782 | |||||||||
Construct_product | WBCnstr00024782 | ||||||||
Microarray_results (19) | |||||||||
Expression_cluster (100) | |||||||||
Map_info | Positive | Positive_clone | W02B3 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | III | -26.2854 | |||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00055090 | |||||||||
WBPaper00062840 | |||||||||
WBPaper00065080 | |||||||||
Method | Gene |