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WormBase Tree Display for Variation: WBVar02148208

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Name Class

WBVar02148208NamePublic_nametm10452
Other_nameF56D6.2.1:c.1025_1089delinsAC
F56D6.2.2:c.1025_1089delinsAC
CE31546:p.Leu342_Leu363delinsHis
HGVSgCHROMOSOME_IV:g.3923906_3923970delinsAC
Sequence_detailsSMapS_parentSequenceF56D6
Flanking_sequencesaacaagtttagttcattggatggatgccactctccaatgtccgtgccacgatatgctcag
Mapping_targetF56D6
Source_location7CHROMOSOME_IV39239053923971Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationInsertionAC
Deletion
PCR_producttm10452_external
tm10452_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq10452
NBP_allele
StatusLive
AffectsGeneWBGene00018971
TranscriptF56D6.2.2VEP_consequenceprotein_altering_variant
VEP_impactMODERATE
HGVScF56D6.2.2:c.1025_1089delinsAC
HGVSpCE31546:p.Leu342_Leu363delinsHis
cDNA_position1055-1119
CDS_position1025-1089
Protein_position342-363
Exon_number7/11
Codon_changecTACGCGAAAGATATCCGATTTATGCCGTCAATCCAAAAGTATCAGGACAAGGATCTCAGACACTT/cAC
Amino_acid_changeLRERYPIYAVNPKVSGQGSQTL/H
F56D6.2.1VEP_consequenceprotein_altering_variant
VEP_impactMODERATE
HGVScF56D6.2.1:c.1025_1089delinsAC
HGVSpCE31546:p.Leu342_Leu363delinsHis
cDNA_position1055-1119
CDS_position1025-1089
Protein_position342-363
Exon_number7/11
Codon_changecTACGCGAAAGATATCCGATTTATGCCGTCAATCCAAAAGTATCAGGACAAGGATCTCAGACACTT/cAC
Amino_acid_changeLRERYPIYAVNPKVSGQGSQTL/H
IsolationMutagenTMP/UV
GeneticsMapIV
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National BioResource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Remark33706/33707-AC-33771/33772 (65 bp deletion + 2 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