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WormBase Tree Display for Variation: WBVar00089537

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Name Class

WBVar00089537NamePublic_namen490
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00026888
WBStrain00026889
WBStrain00026890
WBStrain00026891
LaboratoryMT
StatusLive
Linked_toWBVar00089538
WBVar00089539
WBVar01473744
AffectsGeneWBGene00006832
InteractorWBInteraction000518971
WBInteraction000519146
WBInteraction000537482
WBInteraction000537483
WBInteraction000537484
WBInteraction000537485
WBInteraction000537486
GeneticsMapping_dataIn_2_point778
779
780
In_multi_point702
703
704
821
822
824
825
841
1295
1296
In_pos_neg_data1362
1430
1435
1440
1445
1449
1453
1486
DescriptionPhenotypeWBPhenotype:0000030Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkvery poor growth; n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000154Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
Semi_dominantPaper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
Phenotype_assayGenotypen490/n490Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
WBPhenotype:0000175Paper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
Remarkhypercontracted, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPaper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000229Paper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
Remarksmall, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPaper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Ease_of_scoringES3_Easy_to_scorePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000324Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkshort, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000425Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
RemarkDecreased levels of CED-4 and cytochrome C in mitochondria, Figure 6Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
WBPhenotype:0000546Paper_evidenceWBPaper00002305
Curator_confirmedWBPerson557
WBPhenotype:0000553Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
RemarkThe body wall musculatures of both homozygotes and heterozygotes are structurally disorganized, as revealed by a weak and abnormal birefringency patternPaper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
Semi_dominantPaper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
WBPhenotype:0000583Paper_evidenceWBPaper00002305
Curator_confirmedWBPerson557
WBPhenotype:0000611Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkmuscle hyperactivated, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000634Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarksticky pumping, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000643Paper_evidenceWBPaper00049933
WBPaper00002305
Curator_confirmedWBPerson1754
WBPerson557
RemarkFigure 3Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
Severe locomotion defect.Paper_evidenceWBPaper00002305
Curator_confirmedWBPerson557
WBPhenotype:0000644Paper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
RemarkextremelyPaper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
rigid paralytic; n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPaper_evidenceWBPaper00000914
Person_evidenceWBPerson261
Curator_confirmedWBPerson48
WBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000926Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkabnormal muscle structure, n490/+ similar but less severe phenotypePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Semi_dominantPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Variation_effectNeomorph_gain_of_functionPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0001328Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
Remarkphenotype observed in heterozygotes, but not in homozygotesPaper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
Phenotype_assayGenotypen490/+Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
WBPhenotype:0001577Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
RemarkFigure 4DPaper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
WBPhenotype:0001645Paper_evidenceWBPaper00040284
WBPaper00049933
Curator_confirmedWBPerson2987
WBPerson1754
RemarkTable 1Paper_evidenceWBPaper00040284
Curator_confirmedWBPerson2987
Increased muscle protein degradation, Figure 1Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
WBPhenotype:0001893Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
RemarkFigure 5Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
WBPhenotype:0002019Paper_evidenceWBPaper00002305
Curator_confirmedWBPerson557
WBPhenotype:0002142Paper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
RemarkFigure 5EPaper_evidenceWBPaper00049933
Curator_confirmedWBPerson1754
Phenotype_not_observedWBPhenotype:0000640Paper_evidenceWBPaper00000914
Curator_confirmedWBPerson48
ReferenceWBPaper00040284
WBPaper00000914
WBPaper00016463
WBPaper00014054
WBPaper00016245
WBPaper00015162
WBPaper00002831
WBPaper00049933
WBPaper00002305
MethodAllele