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WormBase Tree Display for Variation: WBVar00250415

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Name Class

WBVar00250415NamePublic_nametm1422
Other_nameB0410.2b.1:c.194_633+45del
B0410.2a.1:c.194_642+45del
HGVSgCHROMOSOME_X:g.2886877_2887472del
Sequence_detailsSMapS_parentSequenceB0410
Flanking_sequencesagattgcaccacctaacgaagactgggcagtttttgggatttttttgctggcttttttta
Mapping_targetB0410
Source_location7CHROMOSOME_X28868762887473Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm1422_external
tm1422_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq1422
NBP_allele
StatusLive
AffectsGeneWBGene00015171
TranscriptB0410.2b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScB0410.2b.1:c.194_633+45del
cDNA_position194-?
CDS_position194-?
Protein_position65-?
Intron_number2-4/7
Exon_number2-4/8
B0410.2a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScB0410.2a.1:c.194_642+45del
cDNA_position208-?
CDS_position194-?
Protein_position65-?
Intron_number3-5/9
Exon_number3-5/10
InteractorWBInteraction000505056
IsolationMutagenTMP/UV
GeneticsMapX
Mapping_dataIn_multi_point5098
DescriptionPhenotypeWBPhenotype:0000061Paper_evidenceWBPaper00040810
Curator_confirmedWBPerson12968
WBPhenotype:0001384Paper_evidenceWBPaper00040810
Curator_confirmedWBPerson12968
WBPhenotype:0001663Paper_evidenceWBPaper00040810
Curator_confirmedWBPerson12968
WBPhenotype:0002490Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the NBP from Dr. A. Colavita: ectopic VC axons.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceOU
EQ_annotationsAnatomy_termWBbt:0005304PATO:0000460Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Phenotype_not_observedWBPhenotype:0000050Paper_evidenceWBPaper00040810
Curator_confirmedWBPerson12968
WBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
WBPhenotype:0000469Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the NBP from Dr. G. Garriga: no obvious HSN or Q neuroblast migration defects.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceNG
WBPhenotype:0000470Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the NBP from Dr. G. Garriga: no obvious HSN or Q neuroblast migration defects.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceNG
WBPhenotype:0000729Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the NBP from Dr. C. Yang: normal cell death phenotype.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFU
WBPhenotype:0001225Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComment to the NBP from Dr. H. Sawa: no Psa phenotype.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceHS
ReferenceWBPaper00040810
Remark1420/1421-2016/2017 (596 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