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WormBase Tree Display for Variation: WBVar00249867

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Name Class

WBVar00249867NamePublic_nametm841
Other_nameC52B9.1b.1:c.867-15_973-150del
C52B9.1a.1:c.930-15_1036-150del
C52B9.1b.2:c.867-15_973-150del
HGVSgCHROMOSOME_X:g.4290489_4290911del
Sequence_detailsSMapS_parentSequenceC52B9
Flanking_sequencesaggttattcatggcgatttgaaattttaaaccgtttttcaaaaccccatttgtaggcaaa
Mapping_targetC52B9
Source_location7CHROMOSOME_X42904884290912Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm841_external
tm841_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq841
NBP_allele
StatusLive
AffectsGeneWBGene00000510
TranscriptC52B9.1a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScC52B9.1a.1:c.930-15_1036-150del
Intron_number7-8/10
Exon_number8/11
C52B9.1b.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScC52B9.1b.2:c.867-15_973-150del
Intron_number6-7/9
Exon_number7/10
C52B9.1b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScC52B9.1b.1:c.867-15_973-150del
Intron_number6-7/9
Exon_number7/10
IsolationMutagenTMP/UV
GeneticsMapX
DescriptionPhenotype_not_observedWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson48
WBPhenotype:0000315Person_evidenceWBPerson7743
Curator_confirmedWBPerson48
RemarkComment from Dr. M. Chalfie: normal touch sensitivity.Person_evidenceWBPerson7743
Curator_confirmedWBPerson48
Remark35053/35054-35476/35477 (423 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