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WormBase Tree Display for Variation: WBVar00249700

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Name Class

WBVar00249700NamePublic_nametm668
Other_nameH15N14.1e.1:c.211_690+13del
H15N14.1d.1:c.211_690+13del
H15N14.1c.1:c.211_897+13del
HGVSgCHROMOSOME_I:g.7774199_7775165del
Sequence_detailsSMapS_parentSequenceH15N14
Flanking_sequencescaacaacaggctcaacaacaagctcagaattttcaaaagctgtacttataaattctcaag
Mapping_targetH15N14
Source_location7CHROMOSOME_I77741987775166Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm668_external
tm668_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00000437
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq668
NBP_allele
StatusLive
AffectsGeneWBGene00000079
TranscriptH15N14.1d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScH15N14.1d.1:c.211_690+13del
cDNA_position233-?
CDS_position211-?
Protein_position71-?
Intron_number4-7/11
Exon_number4-7/12
H15N14.1f.1VEP_consequencecoding_sequence_variant,3_prime_UTR_variant
VEP_impactMODIFIER
cDNA_position211-?
CDS_position211-?
Protein_position71-?
Exon_number3/3
H15N14.1c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScH15N14.1c.1:c.211_897+13del
cDNA_position231-?
CDS_position211-?
Protein_position71-?
Intron_number4-8/14
Exon_number4-8/15
H15N14.1e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScH15N14.1e.1:c.211_690+13del
cDNA_position231-?
CDS_position211-?
Protein_position71-?
Intron_number4-7/13
Exon_number4-7/14
H15N14.1g.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position211-?
CDS_position211-?
Protein_position71-?
Intron_number3-4/4
Exon_number3-5/5
IsolationMutagenTMP/UV
GeneticsMapI
DescriptionPhenotypeWBPhenotype:0000007Paper_evidenceWBPaper00056617
Curator_confirmedWBPerson11281
Phenotype_assayGenotypeunc-22(RNAi)Paper_evidenceWBPaper00056617
Curator_confirmedWBPerson11281
WBPhenotype:0000640Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the National Bioresource Project of Japan from Dr. H. Sawa: Egl.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceHS
WBPhenotype:0000697Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the National Bioresource Project of Japan from Dr. H. Sawa: Pvul.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceHS
WBPhenotype:0000699Paper_evidenceWBPaper00056617
Curator_confirmedWBPerson11281
WBPhenotype:0001171Paper_evidenceWBPaper00056617
Curator_confirmedWBPerson11281
Phenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
ReferenceWBPaper00056617
Remark3992/3993-4959/4960 (967 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
MethodNBP_knockout_allele