Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar00094202

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00094202NamePublic_nameok3124
Other_nameF32E10.5.1:c.578-564_578-191del
F32E10.2.2:c.-6-61_234del
HGVSgCHROMOSOME_IV:g.7576120_7576493del
Sequence_detailsSMapS_parentSequenceF32E10
Flanking_sequencesggatgtgtgcacgtctattcgattcatcgacaatctgatgatagcagcggaggtaatttt
Mapping_targetF32E10
Type_of_mutationDeletion
PCR_productok3124_external
ok3124_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00032979
WBStrain00050681
WBStrain00050687
WBStrain00050688
WBStrain00051706
WBStrain00053675
WBStrain00053676
WBStrain00054542
WBStrain00054543
LaboratoryRB
PersonWBPerson46
KO_consortium_allele
StatusLive
AffectsGeneWBGene00017992
WBGene00017990
TranscriptF32E10.2.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScF32E10.2.2:c.-6-61_234del
cDNA_position?-381
CDS_position?-234
Protein_position?-78
Intron_number1-3/6
Exon_number2-4/7
F32E10.2.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-240
CDS_position?-234
Protein_position?-78
Intron_number2/5
Exon_number1-3/6
F32E10.5.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScF32E10.5.1:c.578-564_578-191del
Intron_number4/7
IsolationMutagenEMS
DescriptionPhenotypeWBPhenotype:0001348Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
RemarkChromosome compaction and intermixing of compartments for chromosome V in embryosPaper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
WBPhenotype:0002636Paper_evidenceWBPaper00048885
Curator_confirmedWBPerson14737
RemarkFigure 1E and Figure 5A-B delocalization of heterochromatic reporter and chromosome arms, respectively; Detachment of H3K9 methylated chromatin from nuclear periphery in early embryosPaper_evidenceWBPaper00048885
Curator_confirmedWBPerson14737
Phenotype_not_observedWBPhenotype:0000050Paper_evidenceWBPaper00048885
Curator_confirmedWBPerson14737
WBPhenotype:0000054Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
WBPhenotype:0000059Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
WBPhenotype:0000062Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
WBPhenotype:0000824Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
WBPhenotype:0008001Paper_evidenceWBPaper00059355
Curator_confirmedWBPerson401
Disease_infoModifies_diseaseDOID:11726
Modifies_disease_in_annotationWBDOannot00000948
ReferenceWBPaper00048885
WBPaper00059355
WBPaper00065293
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele