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WormBase Tree Display for Variation: WBVar00239370

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Name Class

WBVar00239370EvidencePerson_evidenceWBPerson692
NamePublic_namepk1426
Other_nameF10B5.7.1:c.1028+16_3735del
HGVSgCHROMOSOME_II:g.8163749_8166763del
Sequence_detailsSMapS_parentSequenceF10B5
Flanking_sequencescacagtttgtagtgtgtaagttgcacatatatgatgtcaggtggaaaaccgatgtactac
Mapping_targetF10B5
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
Strain (18)
LaboratoryNL
StatusLive
AffectsGeneWBGene00004510
TranscriptF10B5.7.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF10B5.7.1:c.1028+16_3735del
cDNA_position?-3828
CDS_position?-3735
Protein_position?-1245
Intron_number5-11/16
Exon_number6-12/17
Interactor (121)
IsolationMutagenTMP/UV
GeneticsInterpolated_map_positionII0.737993
DescriptionPhenotype (19)
Phenotype_not_observedWBPhenotype:0000039Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Variation_effectNullPaper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Phenotype_assayTreatmentControl RNAi (bacteria not expressing any dsRNA).Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Temperature20Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
WBPhenotype:0000436Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
RemarkDAF-16::GFP was localized in both the cytoplasm and nuclei of all tissues at all developmental stages, like that in wild-type control animals.Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Phenotype_assayGenotypedaf-16::GFPPaper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
WBPhenotype:0000679Paper_evidenceWBPaper00035228
Curator_confirmedWBPerson712
RemarkPGL-1 staining in the germline resembles wild type and appear associated with nuclei periphery.Paper_evidenceWBPaper00035228
Curator_confirmedWBPerson712
WBPhenotype:0000693Paper_evidenceWBPaper00035246
Curator_confirmedWBPerson2021
Remarkrrf-3(pk1426) males produced sperm that were capable of fertilizationPaper_evidenceWBPaper00035246
Curator_confirmedWBPerson2021
WBPhenotype:0001256Paper_evidenceWBPaper00035246
Curator_confirmedWBPerson2021
RemarkSimilar patterns in N2 and rrf-3(pk1426) RAD-51 foci counts suggest successful DNA double strand breaks (DSBs) repairPaper_evidenceWBPaper00035246
Curator_confirmedWBPerson2021
WBPhenotype:0001759Paper_evidenceWBPaper00031962
WBPaper00031961
Curator_confirmedWBPerson712
RemarkThese proteins are not required for piRNA expression, as determined by comparable levels of 21U-RNA on Northern blot and or qRT-PCR to that of wild-type.Paper_evidenceWBPaper00031962
Curator_confirmedWBPerson712
21U-RNAs were expressed normally, as determined by Northern blot analysis.Paper_evidenceWBPaper00031961
Curator_confirmedWBPerson712
EQ_annotationsGO_termGO:0034585PATO:0000460Paper_evidenceWBPaper00031962
Curator_confirmedWBPerson712
WBPhenotype:0001779Paper_evidenceWBPaper00027057
Curator_confirmedWBPerson712
RemarkStrains depleted of RRF-3 do not exhibit accumulation of the precursor miRNA species.Paper_evidenceWBPaper00027057
Curator_confirmedWBPerson712
WBPhenotype:0002146Paper_evidenceWBPaper00027057
Curator_confirmedWBPerson712
RemarkThe accumulation of at least eight small RNAs corresponding to germline-expressed genes, including T01A4.3, did not appear to require this gene.Paper_evidenceWBPaper00027057
Curator_confirmedWBPerson712
WBPhenotype:0002535Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
RemarkPresence and morphology of ciliated neurons were assayed by DiO.Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Phenotype_assayTreatmentAnimals were maintained on control bacteria.Paper_evidenceWBPaper00032237
Curator_confirmedWBPerson712
Reference (31)
RemarkOriginal flanking sequences were obtained from Plasterk Lab, 11/05. Subsequent re-sequencing (6/09) gives the flanking sequences currently entered above, which are very similar to those quoted in WBPaper00004981.
MethodDeletion_allele