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WormBase Tree Display for Variation: WBVar00142935

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Name Class

WBVar00142935NamePublic_namee51
Other_name (18)
HGVSgCHROMOSOME_I:g.7434408C>T
Sequence_detailsSMapS_parentSequenceC44E1
Flanking_sequencesAAGATGACACTCACCAATATGATGAAGTTGATCGTGGATCCGAGTATCTTTCACAAGAACACCATCAGTAGATAGAACAG
Mapping_targetC44E1
Type_of_mutationSubstitutionCTPerson_evidenceWBPerson26471
SeqStatusSequenced
Variation_typeEngineered_allele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000461
WBStrain00000462
WBStrain00000463
WBStrain00000465
WBStrain00000466
WBStrain00000467
WBStrain00000468
WBStrain00000469
WBStrain00000470
WBStrain00000471
WBStrain00000472
WBStrain00000473
WBStrain00000474
WBStrain00000477
WBStrain00000481
WBStrain00000482
WBStrain00000483
WBStrain00000493
WBStrain00003935
WBStrain00003938
WBStrain00004086
WBStrain00004960
WBStrain00005004
WBStrain00006206
WBStrain00006261
WBStrain00007186
WBStrain00007300
WBStrain00007986
WBStrain00007987
WBStrain00008014
WBStrain00022553
WBStrain00022567
WBStrain00022569
WBStrain00022576
WBStrain00023813
WBStrain00023902
WBStrain00023924
WBStrain00023925
WBStrain00023926
WBStrain00023927
WBStrain00023928
WBStrain00023929
WBStrain00023930
WBStrain00023931
WBStrain00023936
WBStrain00023941
WBStrain00023942
WBStrain00027013
WBStrain00027039
WBStrain00027077
WBStrain00027308
WBStrain00028972
WBStrain00030685
WBStrain00033905
WBStrain00034438
WBStrain00034776
WBStrain00034777
WBStrain00040443
WBStrain00047195
WBStrain00050644
WBStrain00050645
WBStrain00055671
WBStrain00057280
WBStrain00057282
LaboratoryCB
KR
NCA
PersonWBPerson26471
StatusLive
Linked_toWBVar02146566
AffectsGeneWBGene00006752
TranscriptZK524.2e.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2e.1:c.1411C>T
HGVSpCE34626:p.Arg471Ter
cDNA_position1411
CDS_position1411
Protein_position471
Exon_number11/30
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2c.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2c.1:c.388C>T
HGVSpCE34624:p.Arg130Ter
cDNA_position388
CDS_position388
Protein_position130
Exon_number3/22
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2f.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2f.1:c.1420C>T
HGVSpCE43866:p.Arg474Ter
cDNA_position1420
CDS_position1420
Protein_position474
Exon_number11/30
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2j.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2j.1:c.1375C>T
HGVSpCE51718:p.Arg459Ter
cDNA_position1375
CDS_position1375
Protein_position459
Exon_number11/29
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2k.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2k.1:c.1366C>T
HGVSpCE51726:p.Arg456Ter
cDNA_position1366
CDS_position1366
Protein_position456
Exon_number11/29
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2a.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2a.1:c.1411C>T
HGVSpCE15371:p.Arg471Ter
cDNA_position1411
CDS_position1411
Protein_position471
Exon_number11/30
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2i.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2i.1:c.1420C>T
HGVSpCE32552:p.Arg474Ter
cDNA_position1420
CDS_position1420
Protein_position474
Exon_number11/29
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2d.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2d.1:c.1411C>T
HGVSpCE34625:p.Arg471Ter
cDNA_position1411
CDS_position1411
Protein_position471
Exon_number11/31
Codon_changeCga/Tga
Amino_acid_changeR/*
ZK524.2h.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScZK524.2h.1:c.388C>T
HGVSpCE51759:p.Arg130Ter
cDNA_position388
CDS_position388
Protein_position130
Exon_number3/21
Codon_changeCga/Tga
Amino_acid_changeR/*
InteractorWBInteraction000518950
IsolationMutagenEMS
GeneticsInterpolated_map_positionI2.07389
Mapping_dataIn_2_point (20)
In_multi_point (87)
In_pos_neg_data466
470
2514
5851
5853
5963
8066
8086
DescriptionPhenotype (13)
Phenotype_not_observedWBPhenotype:0000640Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkable to lay eggsPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0001426Paper_evidenceWBPaper00030754
WBPaper00004883
Curator_confirmedWBPerson712
Remarkas measured by fluorescence levels of ANF::GFP in coelomocytesPaper_evidenceWBPaper00030754
Curator_confirmedWBPerson712
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Phenotype_assayGenotypeEG3683 unc-13(e51) oxIs206[Paex-3:ANF::GFP]Paper_evidenceWBPaper00030754
Curator_confirmedWBPerson712
arIs37Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
WBPhenotype:0001512Paper_evidenceWBPaper00031992
Curator_confirmedWBPerson712
RemarkON-OFF asymmetry of ASEL and ASER was preserved in each of these animals.Paper_evidenceWBPaper00031992
Curator_confirmedWBPerson712
WBPhenotype:0001645Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
RemarkTable S2Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
Reference (29)
Remark (2)
MethodSubstitution_allele