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WormBase Tree Display for Variation: WBVar00250352

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Name Class

WBVar00250352NamePublic_nametm1357
Other_nameY59A8B.7.1:c.148-52_315+305delinsAATA
HGVSgCHROMOSOME_V:g.18045644_18046168delinsAATA
Sequence_detailsSMapS_parentSequenceY59A8B
Flanking_sequencesattgcaaatttctaggtaaacctcaaaattaggatctttacactgtgtatttactcataa
Mapping_targetY59A8B
Source_location7CHROMOSOME_V1804564318046169Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionAATA
Deletion
PCR_producttm1357_external
tm1357_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq1357
NBP_allele
StatusLive
AffectsGeneWBGene00305846
WBGene00305847
WBGene00013344
WBGene00305845
TranscriptY59A8B.45
Y59A8B.7.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScY59A8B.7.1:c.148-52_315+305delinsAATA
Intron_number2-3/6
Exon_number3/7
Y59A8B.44
Y59A8B.46
IsolationMutagenTMP/UV
GeneticsMapV
DescriptionPhenotypeWBPhenotype:0000640Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment from Dr. J. Ahringer to the National Bioresource Project of Japan: weak Egl.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
WBPhenotype:0000646Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment from Dr. J. Ahringer to the National Bioresource Project of Japan: sluggish.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Phenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
Remark116089/116090-AATA-116614/116615 (525 bp deletion + 4 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