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WormBase Tree Display for Variation: WBVar00250940

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Name Class

WBVar00250940NamePublic_nametm1980
Other_nameY69E1A.7c.1:c.14-967_159+19delinsT
HGVSgCHROMOSOME_IV:g.10962941_10964072delinsA
Sequence_detailsSMapS_parentSequenceY69E1A
Flanking_sequencesagtacttgtgtcatagattatgctcatgaaaacacgatagatgtgacatcataaatgtgc
Mapping_targetY69E1A
Source_location7CHROMOSOME_IV1096294010964073Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionA
Deletion
PCR_producttm1980_external
tm1980_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq1980
NBP_allele
StatusLive
AffectsGeneWBGene00000171
WBGene00201914
TranscriptY69E1A.7b.1VEP_consequencesplice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number1/4
Exon_number1/5
Y69E1A.14VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
Y69E1A.7c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScY69E1A.7c.1:c.14-967_159+19delinsT
Intron_number2-3/7
Exon_number3/8
Y69E1A.7a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
Intron_number1-2/6
Exon_number1-2/7
IsolationMutagenTMP/UV
GeneticsMapIV
Mapping_dataIn_multi_point5510
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkHomozygous viable. Originally classified as lethal OR sterile by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
Remark19748/19749-A-20880/20881 (1132 bp deletion + 1 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