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WormBase Tree Display for Variation: WBVar00249494

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Name Class

WBVar00249494NamePublic_nametm448
Other_nameW06B3.2d.1:c.335-78_490delinsC
W06B3.2a.1:c.482-78_637delinsC
W06B3.2b.1:c.482-78_637delinsC
W06B3.2c.1:c.551-78_706delinsC
W06B3.2e.1:c.551-78_706delinsC
W06B3.2a.2:c.482-78_637delinsC
W06B3.2f.1:c.335-78_490delinsC
HGVSgCHROMOSOME_X:g.11999375_12000158delinsG
Sequence_detailsSMapS_parentSequenceW06B3
Flanking_sequencesgaagagttccatcttggttaacaagcaagttgtatagtgggtataatacacccaacacaa
Mapping_targetW06B3
Source_location7CHROMOSOME_X1199937412000159Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionG
Deletion
PCR_producttm448_external
tm448_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq448
NBP_allele
StatusLive
AffectsGeneWBGene00004859
TranscriptW06B3.2b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2b.1:c.482-78_637delinsC
cDNA_position?-681
CDS_position?-637
Protein_position?-213
Intron_number4-5/9
Exon_number5-6/10
W06B3.2f.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2f.1:c.335-78_490delinsC
cDNA_position?-495
CDS_position?-490
Protein_position?-164
Intron_number3-4/8
Exon_number4-5/9
W06B3.2e.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2e.1:c.551-78_706delinsC
cDNA_position?-706
CDS_position?-706
Protein_position?-236
Intron_number4-5/9
Exon_number5-6/10
W06B3.2d.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2d.1:c.335-78_490delinsC
cDNA_position?-495
CDS_position?-490
Protein_position?-164
Intron_number3-4/9
Exon_number4-5/10
W06B3.2c.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2c.1:c.551-78_706delinsC
cDNA_position?-706
CDS_position?-706
Protein_position?-236
Intron_number4-5/8
Exon_number5-6/9
W06B3.2a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2a.1:c.482-78_637delinsC
cDNA_position?-679
CDS_position?-637
Protein_position?-213
Intron_number4-5/10
Exon_number5-6/11
W06B3.2a.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScW06B3.2a.2:c.482-78_637delinsC
cDNA_position?-1251
CDS_position?-637
Protein_position?-213
Intron_number5-6/11
Exon_number6-7/12
IsolationMutagenTMP/UV
GeneticsMapX
DescriptionPhenotypeWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as lethal OR sterile by the National Bioresource Project of Japan. Comment to the NBP from Dr. Y. Ohshima: Development, 132, 3175 (2005).Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
WBPhenotype:0000688Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as lethal OR sterile by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Remark934/935-G-1718/1719 (784 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