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WormBase Tree Display for Variation: WBVar00091860

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Name Class

WBVar00091860EvidencePaper_evidenceWBPaper00032446
NamePublic_nameok574
Other_nameF11D5.3b.1:c.1842-114_*181delinsAATTTAATAGGAAAAAA
F11D5.3a.1:c.1932-114_*181delinsAATTTAATAGGAAAAAA
HGVSgCHROMOSOME_X:g.3323338_3324145delinsAATTTAATAGGAAAAAA
Sequence_detailsSMapS_parentSequenceF11D5
Flanking_sequencesatagtggtgtaaatttaataggaaaaataaatcggtgcccaattgagaattatcaatgta
Mapping_targetF11D5
Type_of_mutationInsertionAATTTAATAGGAAAAAA
Deletion
PCR_productOK574_external
OK574_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00031501
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00017381
TranscriptF11D5.3b.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number13-14/14
Exon_number14-15/15
F11D5.3b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScF11D5.3b.1:c.1842-114_*181delinsAATTTAATAGGAAAAAA
cDNA_position?-3308
Intron_number12-13/14
Exon_number13-15/15
F11D5.3a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScF11D5.3a.1:c.1932-114_*181delinsAATTTAATAGGAAAAAA
cDNA_position?-2608
Intron_number13-14/15
Exon_number14-16/16
InteractorWBInteraction000573249
WBInteraction000573250
IsolationMutagenTMP/UV
DescriptionPhenotypeWBPhenotype:0001224Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
Remarkddr-2(ok574) mutants exhibit weak guidance defects in axons extending along the major longitudinal axon tracts, most prominently the left ventral nerve cord (VNC).Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
WBPhenotype:0001911Paper_evidenceWBPaper00050526
Curator_confirmedWBPerson1068
EQ_annotationsGO_termGO:0031103PATO:0001511Paper_evidenceWBPaper00050526
Curator_confirmedWBPerson1068
Phenotype_not_observedWBPhenotype:0001652Paper_evidenceWBPaper00032446
Curator_confirmedWBPerson2021
ReferenceWBPaper00032446
WBPaper00050526
WBPaper00053867
RemarkLast updated on 29 Nov 2002
Knockout originally requested for F11D5.3 before it was renamed to F11D5.3a
Sequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele