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WormBase Tree Display for Variation: WBVar00242730

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Name Class

WBVar00242730EvidencePaper_evidenceWBPaper00032114
NamePublic_namesm151
Other_nameCE10580:p.Met140Ile
F46A9.5.1:c.420G>A
HGVSgCHROMOSOME_I:g.9472212G>A
Sequence_detailsSMapS_parentSequenceF30A10
Flanking_sequencescttgatgttacctgcaagactgttgctaacatatcaagggaaaatctccagaagagattcgtc
Mapping_targetF30A10
Type_of_mutationSubstitutiongaPaper_evidenceWBPaper00032114
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00005195
LaboratoryCU
StatusLive
AffectsGeneWBGene00004807
TranscriptF46A9.5.1 (12)
IsolationMutagenEMS
GeneticsInterpolated_map_positionI3.76797
DescriptionPhenotype_not_observedWBPhenotype:0000700Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
RemarkNot MuvPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
WBPhenotype:0000822Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Remarksm151 hermaphrodites and males alone do not exhibit any defects in sex-determinationPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
WBPhenotype:0001218Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Remarksm151 hermaphrodites and males alone do not exhibit any defects in sex-specific apoptosisPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Phenotype_assayGenotypesmIs26 [pkd-2p::gfp]Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
WBPhenotype:0001224Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
RemarkNo defects in AVL GABAergic neuron axon outgrowthPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Phenotype_assayGenotypeoxIs12[unc-47::GFP]Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
WBPhenotype:0001586Paper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Remarkno 2ACPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00032114
Curator_confirmedWBPerson2021
ReferenceWBPaper00032114
MethodSubstitution_allele