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WormBase Tree Display for Variation: WBVar00090992

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Name Class

WBVar00090992EvidencePaper_evidenceWBPaper00026736
NamePublic_namene1350
Other_name (12)
HGVSgCHROMOSOME_III:g.13720113C>T
Sequence_detailsSMapS_parentSequenceW06F12
Flanking_sequencesttgcaaatttccaggtcagtaacagatccgggagtggaaaacgagtagctctcaaaaaaa
Mapping_targetW06F12
Type_of_mutationSubstitutionctPaper_evidenceWBPaper00026736
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryWM
StatusLive
AffectsGeneWBGene00003048
TranscriptW06F12.1a.1 (12)
W06F12.1c.1 (12)
W06F12.1b.1 (12)
W06F12.1e.1 (12)
W06F12.1d.2 (12)
W06F12.1d.1 (12)
W06F12.1d.3 (12)
GeneticsInterpolated_map_positionIII21.3992
DescriptionPhenotypeWBPhenotype:0000050Paper_evidenceWBPaper00026736
Curator_confirmedWBPerson2021
RemarkMutants have defects in P2/EMS signalingPaper_evidenceWBPaper00026736
Curator_confirmedWBPerson2021
EQ_annotationsLife_stageWBls:0000003PATO:0000460Paper_evidenceWBPaper00026736
Curator_confirmedWBPerson2021
Temperature_sensitiveHeat_sensitive25CPaper_evidenceWBPaper00026736
Curator_confirmedWBPerson2021
Phenotype_assayTemperature25CPaper_evidenceWBPaper00026736
Curator_confirmedWBPerson2021
ReferenceWBPaper00026736
MethodSubstitution_allele