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WormBase Tree Display for Variation: WBVar00145917

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Name Class

WBVar00145917NamePublic_namegk549
Other_nameF57A10.3.1:c.1060+246_1389-239del
HGVSgCHROMOSOME_V:g.15762749_15763889del
Sequence_detailsSMapS_parentSequenceF57A10
Flanking_sequencesttttttaataagtttaatcacatttttcgggtaatttctctttttttttaaaaagacttt
Mapping_targetF57A10
Type_of_mutationDeletion
PCR_productgk549_external
gk549_internal
SeqStatusSequenced
Deletion_verificationPCR with one primer internal to the deletion and one external confirms that no WT copy of the gene remains.Person_evidenceWBPerson154
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00036397
LaboratoryVC
PersonWBPerson427
KO_consortium_allele
StatusLive
AffectsGeneWBGene00001813
WBGene00201841
TranscriptF57A10.9VEP_consequencetranscript_ablation
VEP_impactHIGH
Exon_number1/1
F57A10.3.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,intron_variant
VEP_impactHIGH
HGVScF57A10.3.1:c.1060+246_1389-239del
Intron_number8-10/15
Exon_number9-10/16
InteractorWBInteraction000537506
IsolationMutagenUV/TMP
DescriptionPhenotype_not_observedWBPhenotype:0002423Paper_evidenceWBPaper00049307
Curator_confirmedWBPerson2987
Remark"Mutations in ABC transporters for other organelles such as haf-2 and haf-3 did not suppress m-nonN-Nmnat1 protection against hypoxia (Supplementary Figure S4b)."Paper_evidenceWBPaper00049307
Curator_confirmedWBPerson2987
EQ_annotationsGO_termGO:0001666PATO:0000460Paper_evidenceWBPaper00049307
Curator_confirmedWBPerson2987
Phenotype_assayGenotypegcIs30[Neuro-m-nonN-Nmnat1]Paper_evidenceWBPaper00049307
Curator_confirmedWBPerson2987
ReferenceWBPaper00049307
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele