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WormBase Tree Display for Variation: WBVar00091509

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Name Class

WBVar00091509EvidencePaper_evidenceWBPaper00039866
NamePublic_nameok200
HGVSgCHROMOSOME_IV:g.11800544_11801794del
Sequence_detailsSMapS_parentSequenceH01G02
Flanking_sequencesaaactcacttttgaaacattcgggaccattgatgaagatcatggaacgttgcaatcaatt
Mapping_targetH01G02
Type_of_mutationDeletion
PCR_productOK200_external
OK200_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00007240
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00045108
WBGene00010349
TranscriptH01G02.4.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position886-?
Intron_number6/6
Exon_number6-7/7
H01G02.4.1VEP_consequence3_prime_UTR_variant
VEP_impactMODIFIER
cDNA_position886-?
Exon_number6/6
H01G02.2.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-206
CDS_position?-116
Protein_position?-39
Intron_number2/8
Exon_number1-3/9
InteractorWBInteraction000563598
WBInteraction000579025
WBInteraction000579026
IsolationMutagenUV/TMP
DescriptionPhenotypeWBPhenotype:0000249Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
RemarkThe strain was impaired in its ability to avoid substances of high osmolarity (Osm phenotype).Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
WBPhenotype:0000255Paper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
Remarksuppression of dye filling defectivePaper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
EQ_annotationsAnatomy_termWBbt:0005391PATO:0000460Paper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
WBbt:0005425PATO:0000460Paper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
WBPhenotype:0000436Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
RemarkThe dyf-18 (ok200) mutant showed prominent accumulations of the homodimeric kinesin-II motor, OSM-3, between the middle and the distal segment both in the amphid and phasmid neuron cilia in 100% of the mutant worms. The IFT protein OSM-5, on the other hand, was frequently observed to accumulate at the base of cilia in amphid and phasmid neurons, with much reduced localization along the ciliary axoneme.Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
WBPhenotype:0000615Paper_evidenceWBPaper00039866
WBPaper00056552
Curator_confirmedWBPerson712
WBPerson35872
RemarkThe structure of most cilia appeared superficially similar to wild type, with occasionally long curved cilia.Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
long and unbranched AWA ciliaPaper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
EQ_annotationsAnatomy_termWBbt:0005670PATO:0000460Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
GO_termGO:0005929PATO:0000573Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
PATO:0000414Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
WBPhenotype:0000854Paper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
EQ_annotationsGO_termGO:0042073PATO:0000460Paper_evidenceWBPaper00054177
Curator_confirmedWBPerson22262
WBPhenotype:0002471Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
Remarklong and unbranched AWA ciliaPaper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
EQ_annotationsAnatomy_termWBbt:0005670PATO:0000460Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
GO_termGO:0005929PATO:0000573Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
PATO:0000414Paper_evidenceWBPaper00056552
Curator_confirmedWBPerson35872
WBPhenotype:0002535Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
RemarkCompared to wild-type animals, ok200 mutant animals display only a weak ability to uptake the dye in amphid (head) and phasmid (tail) neurons.Paper_evidenceWBPaper00039866
Curator_confirmedWBPerson712
ReferenceWBPaper00039866
WBPaper00054177
WBPaper00056552
WBPaper00065813
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele