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WormBase Tree Display for Variation: WBVar02146372

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Name Class

WBVar02146372EvidencePaper_evidenceWBPaper00049562
NamePublic_namen5823
Other_nameZK593.8.1:c.862_869del
CE28722:p.Glu288AsnfsTer10
HGVSgCHROMOSOME_IV:g.10939085_10939092del
Sequence_detailsSMapS_parentSequenceZK593
Flanking_sequencesttatcacttggacaaactcgtgcaatactcaatggttattcccggaaaaagtattcgtgaa
Mapping_targetZK593
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeEngineered_allele
OriginSpeciesCaenorhabditis elegans
LaboratoryMT
Production_methodCRISPR_Cas9
StatusLive
AffectsGeneWBGene00014004
TranscriptZK593.8.1VEP_consequenceframeshift_variant
VEP_impactHIGH
HGVScZK593.8.1:c.862_869del
HGVSpCE28722:p.Glu288AsnfsTer10
cDNA_position880-887
CDS_position862-869
Protein_position288-290
Exon_number6/8
Codon_changeGAATCAGGa/a
Amino_acid_changeESG/X
InteractorWBInteraction000535398
DescriptionPhenotypeWBPhenotype:0002164Paper_evidenceWBPaper00049562
Curator_confirmedWBPerson33753
Remarkanimals are more susceptible to PA14 infectionPaper_evidenceWBPaper00049562
Curator_confirmedWBPerson33753
Phenotype_not_observedWBPhenotype:0001574Paper_evidenceWBPaper00061504
Curator_confirmedWBPerson712
RemarkNeither fic-1 knock-out worms nor worms expressing low or high levels of the constitutive AMPylase FIC-1(E274G) show significant differences in ATP levels compared to N2 controls (Fig. 1B).Paper_evidenceWBPaper00061504
Curator_confirmedWBPerson712
ReferenceWBPaper00049562
WBPaper00061504
MethodEngineered_allele