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WormBase Tree Display for Gene: WBGene00020927

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Name Class

WBGene00020927SMapS_parentSequenceW02B3
IdentityVersion2
NameSequence_nameW02B3.7
Molecular_nameW02B3.7
W02B3.7.1
CE47811
Other_nameCELE_W02B3.7Accession_evidenceNDBBX284603
Public_nameW02B3.7
DB_infoDatabaseAceViewgene3B306
WormQTLgeneWBGene00020927
WormFluxgeneWBGene00020927
NDBlocus_tagCELE_W02B3.7
PanthergeneCAEEL|WormBase=WBGene00020927|UniProtKB=Q09343
familyPTHR15407
NCBIgene189107
RefSeqproteinNM_064838.4
SwissProtUniProtAccQ09343
UniProt_GCRPUniProtAccQ09343
OMIMgene607440
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
204 Sep 2012 09:55:56WBPerson1849EventAcquires_mergeWBGene00020925
Acquires_mergeWBGene00020925
StatusLive
Gene_infoBiotypeSO:0001217
Allele (137)
RNASeq_FPKM (74)
GO_annotation00053427
00053428
00053429
Ortholog (30)
ParalogWBGene00011554Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020307Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020924Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021249Caenorhabditis 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_CDSW02B3.7
Corresponding_CDS_historyW02B3.7:wp233
Corresponding_transcriptW02B3.7.1
Associated_featureWBsf991125
WBsf991126
WBsf991127
WBsf1014113
WBsf1014114
WBsf1014115
Experimental_infoRNAi_resultWBRNAi00006646Inferred_automaticallyRNAi_primary
WBRNAi00054568Inferred_automaticallyRNAi_primary
WBRNAi00019496Inferred_automaticallyRNAi_primary
WBRNAi00019495Inferred_automaticallyRNAi_primary
WBRNAi00036178Inferred_automaticallyRNAi_primary
WBRNAi00006665Inferred_automaticallyRNAi_primary
WBRNAi00054570Inferred_automaticallyRNAi_primary
Expr_patternExpr1014268
Expr1158114
Expr1158116
Expr2006685
Expr2024902
Drives_constructWBCnstr00024781
Construct_productWBCnstr00024781
Microarray_results (29)
Expression_cluster (54)
Interaction (31)
Map_infoPositivePositive_cloneW02B3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIII-26.28
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00065080
MethodGene