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WormBase Tree Display for Gene: WBGene00001164

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Name Class

WBGene00001164SMapS_parentSequenceF15A2
IdentityVersion1
NameCGC_nameefn-3Person_evidenceWBPerson893
Sequence_nameF15A2.5
Molecular_nameF15A2.5
F15A2.5.1
CE44529
Other_nameCELE_F15A2.5Accession_evidenceNDBBX284606
Public_nameefn-3
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classefn
Allele (35)
StrainWBStrain00029134
WBStrain00005372
WBStrain00005375
WBStrain00005671
RNASeq_FPKM (74)
GO_annotation00064874
00064875
00064876
00064877
00064878
00108359
Ortholog (28)
ParalogWBGene00001163Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006869Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001165Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionefn-3 encodes a potential GPI-modified ephrin that is, with EFN-2, is required for normal epidermal organization in the male tail; EFN-3, along with EFN-1 and EFN-2, activates the VAB-1 tyrosine kinase in vivo and binds it in vitro, and has a minor role in embryonic epiboly.Paper_evidenceWBPaper00003865
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable ephrin receptor binding activity. Predicted to be involved in axon guidance and ephrin receptor signaling pathway. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in craniofrontonasal syndrome; dysostosis; and stomach cancer. Is an ortholog of human EFNB1 (ephrin B1).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:1934Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3226)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3226)
DOID:14737Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3226)
Molecular_infoCorresponding_CDSF15A2.5
Corresponding_CDS_historyF15A2.5:wp109
F15A2.5:wp211
Corresponding_transcriptF15A2.5.1
Associated_featureWBsf1007619
WBsf1024237
Experimental_infoRNAi_resultWBRNAi00044670Inferred_automaticallyRNAi_primary
WBRNAi00068189Inferred_automaticallyRNAi_primary
WBRNAi00068216Inferred_automaticallyRNAi_primary
WBRNAi00067728Inferred_automaticallyRNAi_primary
WBRNAi00064787Inferred_automaticallyRNAi_primary
WBRNAi00013336Inferred_automaticallyRNAi_primary
WBRNAi00030979Inferred_automaticallyRNAi_primary
WBRNAi00067850Inferred_automaticallyRNAi_primary
Expr_patternExpr1011959
Expr1148644
Drives_constructWBCnstr00037054
Construct_productWBCnstr00009795
WBCnstr00009796
WBCnstr00037054
Microarray_results (16)
Expression_cluster (145)
Interaction (72)
Map_infoMapXPosition12.6185Error0.012221
PositivePositive_cloneF15A2Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4276
Pseudo_map_position
Reference (21)
RemarkSequence connection from [Wang X, Culotti JG, Pawson T]
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
MethodGene