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WormBase Tree Display for Variation: WBVar00252059

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Name Class

WBVar00252059NamePublic_nametm3364
Other_nameM03F8.2e.1:c.-654+357_-10+87delinsTGAAATTTT
M03F8.2b.1:c.202+357_846+87delinsTGAAATTTT
M03F8.2a.1:c.157+357_801+87delinsTGAAATTTT
M03F8.2d.1:c.157+357_801+87delinsTGAAATTTT
M03F8.2c.1:c.202+357_846+87delinsTGAAATTTT
HGVSgCHROMOSOME_V:g.5945383_5946568delinsTGAAATTTT
Sequence_detailsSMapS_parentSequenceM03F8
Flanking_sequencestttatggctaaatgtatcaattttccctttttgaaattttttgtgaaaaacaatttttgc
Mapping_targetM03F8
Source_location7CHROMOSOME_V59453825946569Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionTGAAATTTT
Deletion
PCR_producttm3364_external
tm3364_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq3364
NBP_allele
StatusLive
AffectsGeneWBGene00004206
TranscriptM03F8.2e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScM03F8.2e.1:c.-654+357_-10+87delinsTGAAATTTT
Intron_number1-3/7
Exon_number2-3/8
M03F8.2d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM03F8.2d.1:c.157+357_801+87delinsTGAAATTTT
Intron_number3-5/8
Exon_number4-5/9
M03F8.2c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM03F8.2c.1:c.202+357_846+87delinsTGAAATTTT
Intron_number2-4/7
Exon_number3-4/8
M03F8.2a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM03F8.2a.1:c.157+357_801+87delinsTGAAATTTT
Intron_number3-5/7
Exon_number4-5/8
M03F8.2b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScM03F8.2b.1:c.202+357_846+87delinsTGAAATTTT
Intron_number3-5/7
Exon_number4-5/8
InteractorWBInteraction000500894
WBInteraction000500895
IsolationMutagenTMP/UV
GeneticsMapV
DescriptionPhenotype (19)
Phenotype_not_observedWBPhenotype:0000047Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
RemarkNo abnormalities were observed for Ea and Ep cell ingression.Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
WBPhenotype:0000748Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
RemarkNo abnormalities in this phenotype were observed in these mutants.Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0004015PATO:0000460Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
WBbt:0006770PATO:0000460Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
WBPhenotype:0001018Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
RemarkNo abnormalities in this phenotype were observed in these mutants.Paper_evidenceWBPaper00036358
Curator_confirmedWBPerson712
ReferenceWBPaper00036358
Remark14054/14055-TGAAATTTT-15240/15241 (1186 bp deletion + 9 bp insertion)
This knockout was generated by the National Bioresource Project, Tokyo, Japan, which is part of the International C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use.Paper_evidenceWBPaper00041807
MethodNBP_knockout_allele