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WormBase Tree Display for Variation: WBVar00251849

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Name Class

WBVar00251849NamePublic_nametm3067
Other_nameC05C8.9b.2:c.-43_345del
C05C8.9a.1:c.-43_345del
C05C8.9b.1:c.-43_345del
HGVSgCHROMOSOME_V:g.7237515_7238007del
Sequence_detailsSMapS_parentSequenceC05C8
Flanking_sequencesgtagtttaacgtgtacgtcatttcctccttcctgagagaaaccttctggtcgatcgagcg
Mapping_targetC05C8
Source_location7CHROMOSOME_V72375147238008Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm3067_external
tm3067_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq3067
NBP_allele
StatusLive
AffectsGeneWBGene00015466
TranscriptC05C8.9b.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,start_lost,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScC05C8.9b.1:c.-43_345del
cDNA_position103-490
CDS_position?-345
Protein_position?-115
Intron_number2-3/5
Exon_number1-4/6
C05C8.9a.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,start_lost,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScC05C8.9a.1:c.-43_345del
cDNA_position135-522
CDS_position?-345
Protein_position?-115
Intron_number2-3/6
Exon_number1-4/7
C05C8.9b.2VEP_consequencesplice_acceptor_variant,splice_donor_variant,start_lost,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
HGVScC05C8.9b.2:c.-43_345del
cDNA_position100-487
CDS_position?-345
Protein_position?-115
Intron_number2-3/4
Exon_number1-4/5
IsolationMutagenTMP/UV
GeneticsMapV
DescriptionPhenotypeWBPhenotype:0000238Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkForaging behavior was reduced compared to controlPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000304Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkChemotaxis to isoamyl alcohol was reduced compared to controlPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000310Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkResidual cilia were not associated with a particular type of neuron; The ASER neuron lacks ciliary projectionsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000425Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkPunctate HYLS-1 staining was absent in hyls-1deletion wormsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000436Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkCHE-11:GFP fails to accumulate at the transition zone of hyls-1 mutantsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000843Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkMale mating efficiency was reduced compared to controlPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0002535Paper_evidenceWBPaper00035062
Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkIn hyls-1 mutant animals, only 10% of the normal number of ciliated neurons were observed to dye-fillPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Comment to the National Bioresource of Japan from Dr. O. Blacque: partially Dyf.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceOEB
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Phenotype_not_observedWBPhenotype:0000062Paper_evidenceWBPaper00035062
Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as homozygous viable by the National Bioresource Project of Japan. Comment to the NBP from Dr. K. Oegema: Genes & Dev. 23, 2046 (2009).Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Laboratory_evidenceFX
OD
hyls-1 mutant embryos were viablePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000688Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Remarkhyls-1 mutant embryos developed into fertile adultsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0000853Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkIFT is unchanged in residual cilia of hyls-1 mutant animalsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0001333Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
RemarkNeuron-specific GFP reporters confirmed normal presence of the amphid and phasmid neurons in hyls-1 mutantsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
WBPhenotype:0001588Paper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Remarkhyls-1 mutant embryos did not show centriole duplication defectsPaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Variation_effectProbable_null_via_phenotypePaper_evidenceWBPaper00035062
Curator_confirmedWBPerson712
Disease_infoModels_diseaseDOID:0050779
Models_disease_in_annotationWBDOannot00000206
ReferenceWBPaper00035062
Remark13498/13499-13991/13992 (493 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