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WormBase Tree Display for Variation: WBVar02151732

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Name Class

WBVar02151732NamePublic_nametm11398
Other_nameF59A2.6d.1:c.1440-629_3531+490del
F59A2.6a.1:c.1566-629_3658-191del
F59A2.6c.1:c.1440-629_3532-191del
F59A2.6b.1:c.1566-629_3657+490del
HGVSgCHROMOSOME_III:g.3416172_3420934del
Sequence_detailsSMapS_parentSequenceCHROMOSOME_III
Flanking_sequencesaattttttttctttgaaattctgaaaaaaaattttccccgatttttctccaatttttggc
Mapping_targetCHROMOSOME_III
Source_location7CHROMOSOME_III34161713420935Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm11398_external
tm11398_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq11398
NBP_allele
StatusLive
AffectsGeneWBGene00219986
WBGene00010306
TranscriptF59A2.6a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF59A2.6a.1:c.1566-629_3658-191del
Intron_number8-14/19
Exon_number9-14/20
F59A2.6c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF59A2.6c.1:c.1440-629_3532-191del
Intron_number7-13/18
Exon_number8-13/19
F59A2.6b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF59A2.6b.1:c.1566-629_3657+490del
Intron_number7-13/17
Exon_number8-13/18
F59A2.7VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
F59A2.6d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF59A2.6d.1:c.1440-629_3531+490del
Intron_number7-13/17
Exon_number8-13/18
IsolationMutagenTMP/UV
GeneticsMapIII
Remark[F59A2]22798/22799-[K01A11]2290/2291 (4763 bp deletion)
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
Old Mapping_target F59A2 updated based on the VEP analysis pipeline to CHROMOSOME_III.
MethodNBP_knockout_allele