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WormBase Tree Display for Variation: WBVar00095115

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Name Class

WBVar00095115EvidencePaper_evidenceWBPaper00005148
NamePublic_namep675
Other_nameC02F4.2a.2:c.775G>A
CE46586:p.Asp259Asn
CE07853:p.Asp259Asn
C02F4.2a.1:c.775G>A
C02F4.2c.1:c.775G>A
CE52450:p.Asp259Asn
C02F4.2b.1:c.775G>A
C02F4.2c.2:c.775G>A
HGVSgCHROMOSOME_IV:g.10498698C>T
Sequence_detailsSMapS_parentSequenceC02F4
Flanking_sequencestttggtccaatgtgtgatcttctctggtcaacccacttgaagatttcggaaacgaaagga
Mapping_targetC02F4
Type_of_mutationSubstitutionga
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00030784
LaboratoryPR
StatusLive
AffectsGeneWBGene00006527
TranscriptC02F4.2c.2 (12)
C02F4.2c.1 (12)
C02F4.2b.1 (12)
C02F4.2a.1 (12)
C02F4.2a.2 (12)
InteractorWBInteraction000500286
WBInteraction000501865
WBInteraction000502332
WBInteraction000502703
WBInteraction000502705
WBInteraction000502707
WBInteraction000504755
GeneticsInterpolated_map_positionIV4.61436
Mapping_dataIn_multi_point4720
DescriptionPhenotype (16)
Phenotype_not_observedWBPhenotype:0000615Paper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
RemarkIn the tax-6(p675) loss-of-function mutant, cilia development, morphology, and OSM-6 motility were intact in amphid, phasmid, and male-specific sensory neurons (unpublished data).Paper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
Variation_effectLoss_of_function_undetermined_extentPaper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
WBPhenotype:0000853Paper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
RemarkIn the tax-6(p675) loss-of-function mutant, cilia development, morphology, and OSM-6 motility were intact in amphid, phasmid, and male-specific sensory neurons (unpublished data).Paper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
Variation_effectLoss_of_function_undetermined_extentPaper_evidenceWBPaper00027106
Curator_confirmedWBPerson712
WBPhenotype: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
Reference (15)
MethodSubstitution_allele