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WormBase Tree Display for Variation: WBVar00091568

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Name Class

WBVar00091568EvidencePaper_evidenceWBPaper00031112
NamePublic_nameok268
Other_name (12)
HGVSgCHROMOSOME_IV:g.17121871_17123529del
Sequence_detailsSMapS_parentSequenceY116A8C
Flanking_sequencescgaatctcaagaactcggccatcagcttctcagtaatatctcaatgtattgcacaattcc
Mapping_targetY116A8C
Type_of_mutationDeletion
PCR_productOK268_external
OK268_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00035580
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00006405
TranscriptY116A8C.36c.1 (11)
Y116A8C.36b.1 (11)
Y116A8C.36a.1 (11)
Y116A8C.36f.1 (11)
Y116A8C.36e.1 (11)
Y116A8C.36d.1 (11)
InteractorWBInteraction000538783
IsolationMutagenUV/TMP
DescriptionPhenotypeWBPhenotype:0000016Paper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
Remarkitsn-1(ok268) and itsn-1(tm725) worms were hypersensitive to aldicarb, in acute and chronic assaysPaper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
Variation_effectNullPaper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
Affected_byMoleculeWBMol:00003650Paper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
EQ_annotationsLife_stageWBls:0000041PATO:0000460Paper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
WBPhenotype:0000436Paper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
RemarkDynamin redistributes, in part, from a soluble to a membrane-bound fraction in an ITSN-1 mutant backgroundPaper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
Variation_effectNullPaper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
Phenotype_assayTreatmentWestern Blots with SNB-1, ITSN-1 and DYN-1 antibodiesPaper_evidenceWBPaper00031112
Curator_confirmedWBPerson2021
WBPhenotype:0000519Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
RemarkNull mutants are viable and display grossly normal locomotion and development. However, motor neurons in these mutants show a dramatic increase in large irregular vesicles and accumulate membrane-associated vesicles at putative endocytic hotspots, approximately 300 nm from the presynaptic density.Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
WBPhenotype:0001323Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
RemarkNull mutants are viable and display grossly normal locomotion and development. However, motor neurons in these mutants show a dramatic increase in large irregular vesicles and accumulate membrane-associated vesicles at putative endocytic hotspots, approximately 300 nm from the presynaptic density.Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
EQ_annotationsAnatomy_termWBbt:0005409PATO:0000460Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
WBPhenotype:0001671Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
RemarkNull mutants are viable and display grossly normal locomotion and development. However, motor neurons in these mutants show a dramatic increase in large irregular vesicles and accumulate membrane-associated vesicles at putative endocytic hotspots, approximately 300 nm from the presynaptic density.Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
EQ_annotationsAnatomy_termWBbt:0005409PATO:0000460Paper_evidenceWBPaper00031546
Curator_confirmedWBPerson7761
Phenotype_not_observed (13)
ReferenceWBPaper00031112
WBPaper00031546
WBPaper00065262
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele