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WormBase Tree Display for Variation: WBVar00249293

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Name Class

WBVar00249293NamePublic_nametm239
Other_nameC33D12.1.1:c.87_437+105del
HGVSgCHROMOSOME_X:g.3069509_3070221del
Sequence_detailsSMapS_parentSequenceCHROMOSOME_X
Flanking_sequencestaatgcactacaattaacacaaagtggcgtccggaagaactctgagcagcaagttggttg
Mapping_targetCHROMOSOME_X
Source_location7CHROMOSOME_X30695083070222Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm239_external
tm239_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq239
NBP_allele
StatusLive
AffectsGeneWBGene00000452
WBGene00202458
TranscriptC33D12.17VEP_consequencenon_coding_transcript_exon_variant
VEP_impactMODIFIER
cDNA_position236-?
Exon_number1/1
C33D12.1.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScC33D12.1.1:c.87_437+105del
cDNA_position202-?
CDS_position87-?
Protein_position29-?
Intron_number2-3/4
Exon_number2-3/5
IsolationMutagenTMP/UV
GeneticsMapX
DescriptionPhenotype (15)
Phenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
WBPhenotype:0000095Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the National Bioresource Project of Japan from Dr. J.K.Lu: no defects in the M lineagePerson_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceKW
ReferenceWBPaper00032309
Remark27769/27770-[F52E4]443/444 (713 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 C33D12 updated based on the VEP analysis pipeline to CHROMOSOME_X.
MethodNBP_knockout_allele