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WormBase Tree Display for Variation: WBVar00252164

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Name Class

WBVar00252164NamePublic_nametm3495
Other_nameF29G6.3f.2:c.183+86_367delinsGATAA
F29G6.3b.1:c.183+86_367delinsGATAA
F29G6.3f.3:c.183+86_367delinsGATAA
F29G6.3c.1:c.183+86_367delinsGATAA
F29G6.3f.1:c.183+86_367delinsGATAA
F29G6.3a.1:c.183+86_367delinsGATAA
HGVSgCHROMOSOME_X:g.11518244_11518648delinsTTATC
Sequence_detailsSMapS_parentSequenceF29G6
Flanking_sequencescaacaacagcttccccaacaacaatcggagataagttatcaaatcagaagtaaaaaaaat
Mapping_targetF29G6
Source_location7CHROMOSOME_X1151824311518649Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionTTATC
Deletion
PCR_producttm3495_external
tm3495_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq3495
NBP_allele
StatusLive
AffectsGeneWBGene00009259
TranscriptF29G6.3b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3b.1:c.183+86_367delinsGATAA
cDNA_position?-413
CDS_position?-367
Protein_position?-123
Intron_number4-6/19
Exon_number5-7/20
F29G6.3c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3c.1:c.183+86_367delinsGATAA
cDNA_position?-367
CDS_position?-367
Protein_position?-123
Intron_number3-5/18
Exon_number4-6/19
F29G6.3a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3a.1:c.183+86_367delinsGATAA
cDNA_position?-410
CDS_position?-367
Protein_position?-123
Intron_number4-6/19
Exon_number5-7/20
F29G6.3d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-94
CDS_position?-94
Protein_position?-32
Intron_number1/13
Exon_number1-2/14
F29G6.3f.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3f.2:c.183+86_367delinsGATAA
cDNA_position?-416
CDS_position?-367
Protein_position?-123
Intron_number4-6/18
Exon_number5-7/19
F29G6.3f.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3f.1:c.183+86_367delinsGATAA
cDNA_position?-416
CDS_position?-367
Protein_position?-123
Intron_number4-6/17
Exon_number5-7/18
F29G6.3f.3VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF29G6.3f.3:c.183+86_367delinsGATAA
cDNA_position?-401
CDS_position?-367
Protein_position?-123
Intron_number4-6/16
Exon_number5-7/17
IsolationMutagenTMP/UV
GeneticsMapX
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
WBPhenotype:0000643Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkComments to the National Bioresource Project of Japan: Dr. R. Aroian: Normal locomotion.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
Remark20621/20622-TTATC-21026/21027 (405 bp deletion + 5 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