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WormBase Tree Display for Variation: WBVar00600869

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Name Class

WBVar00600869NamePublic_nametm5487
Other_nameT21C12.1c.2:c.936_1128+58del
T21C12.1d.1:c.936_1128+58del
T21C12.1e.1:c.936_1129-18del
T21C12.1k.1:c.936_1128+58del
T21C12.1f.1:c.563-1993_563-1692del
T21C12.1c.1:c.936_1128+58del
T21C12.1m.1:c.432_624+58del
T21C12.1o.1:c.59-1993_59-1692del
HGVSgCHROMOSOME_III:g.10528593_10528894del
Sequence_detailsSMapS_parentSequenceT21C12
Flanking_sequencesaaccaataattcgatgccaaaagtgtcttaaacacattcttatttagtcatacgaaatga
Mapping_targetT21C12
Source_location7CHROMOSOME_III1052859210528895Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm5487_external
tm5487_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq5487
NBP_allele
StatusLive
AffectsGeneWBGene00006784
TranscriptT21C12.1k.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1k.1:c.936_1128+58del
cDNA_position936-?
CDS_position936-?
Protein_position312-?
Intron_number7-8/11
Exon_number7-8/12
T21C12.1m.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1m.1:c.432_624+58del
cDNA_position432-?
CDS_position432-?
Protein_position144-?
Intron_number3-4/8
Exon_number3-4/9
T21C12.1c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1c.1:c.936_1128+58del
cDNA_position1142-?
CDS_position936-?
Protein_position312-?
Intron_number8-9/18
Exon_number8-9/19
T21C12.1e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1e.1:c.936_1129-18del
cDNA_position1061-?
CDS_position936-?
Protein_position312-?
Intron_number8-9/19
Exon_number8-9/20
T21C12.1c.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1c.2:c.936_1128+58del
cDNA_position1061-?
CDS_position936-?
Protein_position312-?
Intron_number8-9/14
Exon_number8-9/15
T21C12.1o.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1o.1:c.59-1993_59-1692del
Intron_number1/5
T21C12.1d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScT21C12.1d.1:c.936_1128+58del
cDNA_position1142-?
CDS_position936-?
Protein_position312-?
Intron_number8-9/17
Exon_number8-9/18
T21C12.1f.1VEP_consequenceintron_variant
VEP_impactMODIFIER
HGVScT21C12.1f.1:c.563-1993_563-1692del
Intron_number6/11
IsolationMutagenTMP/UV
GeneticsMapIII
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
Remark7917/7918-8219/8220 (302 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