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WormBase Tree Display for Variation: WBVar00143369

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Name Class

WBVar00143369NamePublic_namee648
Other_nameCE24899:p.Trp101Ter
F14F3.1a.1:c.303G>A
F14F3.1a.2:c.303G>A
HGVSgCHROMOSOME_X:g.10511192G>A
Sequence_detailsSMapS_parentSequenceF14F3
Flanking_sequencesacaaacgtgaccaacctagcatttttgcatggaaatcagagataaactgctagctgataat
Mapping_targetF14F3
Type_of_mutationSubstitutiongaPaper_evidenceWBPaper00002236
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004190
LaboratoryCB
CX
StatusLive
AffectsGeneWBGene00006870
TranscriptF14F3.1a.1VEP_consequencestop_gained
VEP_impactHIGH
HGVScF14F3.1a.1:c.303G>A
HGVSpCE24899:p.Trp101Ter
cDNA_position605
CDS_position303
Protein_position101
Exon_number6/14
Codon_changetgG/tgA
Amino_acid_changeW/*
F14F3.1a.2VEP_consequencestop_gained
VEP_impactHIGH
HGVScF14F3.1a.2:c.303G>A
HGVSpCE24899:p.Trp101Ter
cDNA_position395
CDS_position303
Protein_position101
Exon_number5/13
Codon_changetgG/tgA
Amino_acid_changeW/*
InteractorWBInteraction000003443
IsolationMutagenEMSPaper_evidenceWBPaper00002236
GeneticsInterpolated_map_positionX2.22423
Mapping_dataIn_2_point164
3647
3649
3652
3658
3668
In_multi_point (15)
In_pos_neg_data293
498
874
3646
4979
4981
DescriptionPhenotype (10)
Phenotype_not_observedWBPhenotype:0001660Paper_evidenceWBPaper00006052
Curator_confirmedWBPerson2021
RemarkNo disruption of ASE asymmetry (as seen with lim-6 reporters)Paper_evidenceWBPaper00006052
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00006052
Curator_confirmedWBPerson2021
Phenotype_assayGenotypeotIs114, otIs6Paper_evidenceWBPaper00006052
Curator_confirmedWBPerson2021
ReferenceWBPaper00006052
WBPaper00021796
WBPaper00003665
WBPaper00003760
WBPaper00014771
WBPaper00004825
WBPaper00014973
WBPaper00014314
WBPaper00017246
WBPaper00016625
RemarkThis allele has the same nucleotide mutation at the same position as ky664. It is mutated with the same mutagen as ky664, but obtained using a diferent screen.Paper_evidenceWBPaper00002236
MethodSubstitution_allele