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WormBase Tree Display for Gene: WBGene00020924

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Name Class

WBGene00020924SMapS_parentSequenceW02B3
IdentityVersion1
NameSequence_nameW02B3.4
Molecular_nameW02B3.4
W02B3.4.1
CE34600
Other_nameCELE_W02B3.4Accession_evidenceNDBBX284603
Public_nameW02B3.4
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (87)
StrainWBStrain00003334
RNASeq_FPKM (74)
GO_annotation00053424
00053425
00053426
Ortholog (36)
ParalogWBGene00011554Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00017877Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
WBGene00020307Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00020308Caenorhabditis elegansFrom_analysisTreeFam
WBGene00020309Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
WBGene00021249Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00020927Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00045475Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionAutomated_descriptionPredicted 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_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0050560Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0050559Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0110443Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:9884Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0112379Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0110296Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0110444Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
DOID:0110284Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3622)
Molecular_infoCorresponding_CDSW02B3.4
Corresponding_CDS_historyW02B3.4:wp102
Corresponding_transcriptW02B3.4.1
Other_sequenceAcan_isotig16043
Associated_featureWBsf226121
Experimental_infoRNAi_resultWBRNAi00036177Inferred_automaticallyRNAi_primary
WBRNAi00054567Inferred_automaticallyRNAi_primary
WBRNAi00006634Inferred_automaticallyRNAi_primary
Expr_patternChronogram182
Expr6820
Expr1022840
Expr1158113
Expr2006684
Expr2024901
Drives_constructWBCnstr00003805
WBCnstr00024782
Construct_productWBCnstr00024782
Microarray_results (19)
Expression_cluster (100)
Map_infoPositivePositive_cloneW02B3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIII-26.2854
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00062840
WBPaper00065080
MethodGene