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WormBase Tree Display for Variation: WBVar00146378

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Name Class

WBVar00146378EvidencePaper_evidenceWBPaper00025221
NamePublic_namegu22
Other_nameCE05215:p.Met57Ile
C04G2.7.1:c.171G>A
HGVSgCHROMOSOME_IV:g.10109232C>T
Sequence_detailsSMapS_parentSequenceC04G2
Flanking_sequencestgacacagttcgtgctcaaatagtcgaaattcacaacatggtacacgaccatgtgacata
Mapping_targetC04G2
Type_of_mutationSubstitutiongaPaper_evidenceWBPaper00025221
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryCM
StatusLive
AffectsGeneWBGene00001204
TranscriptC04G2.7.1 (12)
GeneticsInterpolated_map_positionIV4.52959
DescriptionPhenotypeWBPhenotype:0000183Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0005784PATO:0000460Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
Life_stageWBls:0000057PATO:0000460Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
WBPhenotype:0001180Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0005784PATO:0000460Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
Life_stageWBls:0000057PATO:0000460Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
Phenotype_assayTreatmentGermline corpses were quantified in staged adults (generally 24 hours after L4/adult molt) stained with SYTO12.Paper_evidenceWBPaper00028561
Curator_confirmedWBPerson712
WBPhenotype:0001278Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Remarkgu22 affected the expression of lin-48 in hindgut cellsPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Phenotype_assayGenotypesaIs14 [lin-48::GFP]Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
WBPhenotype:0001297Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Remarkgu22 mutants exhibit defective male tail developmentPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
WBPhenotype:0001298Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Remarkgu22 mutants exhibit defective hindgut developmentPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
WBPhenotype:0001372Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Remarkgu22 protein exhibits reduced DNA binding activityPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Phenotype_not_observedWBPhenotype:0000006Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
RemarkMutants retain a high level of function in the egg-laying systemPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
WBPhenotype:0000695Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
RemarkvulF morphogenesis is normalPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
EQ_annotationsAnatomy_termWBbt:0006768PATO:0000460Paper_evidenceWBPaper00025221
Curator_confirmedWBPerson2021
ReferenceWBPaper00028561
WBPaper00025221
MethodSubstitution_allele