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WormBase Tree Display for Variation: WBVar00249802

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Name Class

WBVar00249802NamePublic_nametm774
Other_name (25)
HGVSgCHROMOSOME_V:g.23999_24591del
Sequence_detailsSMapS_parentSequenceB0348
Flanking_sequencesatgtatttttcaaaaaaaaattgccttaacaaaaagaagaaaaccggttgaaaacgataa
Mapping_targetB0348
Source_location7CHROMOSOME_V2399824592Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm774_external
tm774_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq774
NBP_allele
StatusLive
AffectsGeneWBGene00001177
Transcript (25)
IsolationMutagenTMP/UV
GeneticsMapV
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Remark18969/18970-19562/19563 (593 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