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WormBase Tree Display for Variation: WBVar00145526

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Name Class

WBVar00145526EvidencePaper_evidenceWBPaper00026102
NamePublic_namegk119
HGVSgCHROMOSOME_I:g.1842444_1843119delinsTGGAAAAAGCGATTTCAA
Sequence_detailsSMapS_parentSequenceM01D7
Flanking_sequencescttgaaaattgtcattttttgctttttccagttgaaatcgctatttttacccctctccct
Mapping_targetM01D7
Type_of_mutationInsertiontggaaaaagcgatttcaat
Deletion
PCR_productGK119_external
GK119_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00003835
WBStrain00003842
WBStrain00035605
WBStrain00047806
WBStrain00047807
WBStrain00047808
WBStrain00055828
WBStrain00055831
WBStrain00055835
WBStrain00055840
LaboratoryVC
CA
PersonWBPerson427
KO_consortium_allele
StatusLive
AffectsGeneWBGene00001309
TranscriptM01D7.6.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-550
Intron_number2-3/5
Exon_number1-5/6
M01D7.6.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,3_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-550
Intron_number2-3/4
Exon_number1-5/5
InteractorWBInteraction000505178
WBInteraction000544761
WBInteraction000579028
GeneticsMapping_dataIn_multi_point4286
DescriptionPhenotypeWBPhenotype:0000016Paper_evidenceWBPaper00044786
Curator_confirmedWBPerson2987
Affected_byMoleculeWBMol:00003650Paper_evidenceWBPaper00044786
Curator_confirmedWBPerson2987
Disease_infoModels_diseaseDOID:11726
Models_disease_in_annotationWBDOannot00000045
ReferenceWBPaper00026102
WBPaper00044786
WBPaper00065722
RemarkSequenced by the C. elegans Gene Knockout ConsortiumPaper_evidenceWBPaper00041807
MethodKO_consortium_allele