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WormBase Tree Display for Variation: WBVar00143592

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Name Class

WBVar00143592NamePublic_namee912
Other_nameF59G1.4a.1:c.250-263_947-68del
HGVSgCHROMOSOME_II:g.5896964_5902373del
Sequence_detailsSMapS_parentSequenceF59G1
Flanking_sequencesaggaaggaacaagtcgatcggaaaattttattttcacactgggagctagttccaataaaa
Mapping_targetF59G1
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004403
WBStrain00006311
WBStrain00026764
WBStrain00026863
WBStrain00027055
WBStrain00027229
WBStrain00027586
WBStrain00040213
WBStrain00040275
WBStrain00051497
LaboratoryCB
StatusLive
AffectsGeneWBGene00002993
WBGene00198855
WBGene00199631
WBGene00197123
WBGene00019128
TranscriptF59G1.6
F59G1.13VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
F59G1.10VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
F59G1.4a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF59G1.4a.1:c.250-263_947-68del
Intron_number4-10/14
Exon_number5-10/15
F59G1.12VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Interactor (17)
IsolationMutagen
GeneticsInterpolated_map_positionII-0.855656
Mapping_dataIn_2_point40
777
4220
In_multi_point (11)
In_pos_neg_data3708
4223
4224
DescriptionPhenotype (23)
Phenotype_not_observedWBPhenotype:0000207Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
RemarkDefecation cycle is normalPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBPhenotype:0000634Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
RemarkPumping is normalPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBPhenotype:0000637Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
RemarkNo defects in dauer formationPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBPhenotype:0001233Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
RemarkCell number and nuclear staining is normalPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Phenotype_assayTreatmentDAPI stainingPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBPhenotype:0002535Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Remarknon-DyfPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
EQ_annotationsAnatomy_termWBbt:0005666PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0005667PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0005668PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0005665PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0005661PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0007807PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
WBbt:0007808PATO:0000460Paper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Phenotype_assayTreatmentDiO stainingPaper_evidenceWBPaper00031335
Curator_confirmedWBPerson2021
Reference (35)
MethodDeletion_allele