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WormBase Tree Display for Variation: WBVar02148010

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Name Class

WBVar02148010NamePublic_nametm10222
HGVSgCHROMOSOME_III:g.10089047_10098726del
Sequence_detailsSMapS_parentSequenceT16H12
Flanking_sequencesttaaatctgacgtaccctcgtgtcacttcattctgacatgtcaggaagagcctagaaaaa
Mapping_targetT16H12
Source_location7CHROMOSOME_III1008904610098727Inferred_automaticallyNational_Bioresource_Project
Type_of_mutationDeletion
PCR_producttm10222_external
tm10222_internal
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryFX
AuthorMitani S
DB_infoDatabaseNational_Bioresource_Projectseq10222
NBP_allele
StatusLive
AffectsGeneWBGene00002186
WBGene00011815
WBGene00011814
TranscriptT16H12.6.1VEP_consequencecoding_sequence_variant,3_prime_UTR_variant
VEP_impactMODIFIER
cDNA_position1639-?
CDS_position1639-?
Protein_position547-?
Exon_number12-13/13
T16H12.5b.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2-6/7
Exon_number1-8/8
T16H12.5a.1VEP_consequencetranscript_ablation
VEP_impactHIGH
Intron_number2-7/8
Exon_number1-9/9
T16H12.4.1VEP_consequencesplice_acceptor_variant,splice_donor_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant
VEP_impactHIGH
cDNA_position?-992
CDS_position?-986
Protein_position?-329
Intron_number2-9/11
Exon_number1-10/12
IsolationMutagenTMP/UV
GeneticsMapIII
DescriptionPhenotypeWBPhenotype:0000062Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as lethal OR sterile by the National BioResource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
WBPhenotype:0000688Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
RemarkClassified as lethal OR sterile by the National BioResource Project of Japan.Person_evidenceWBPerson7743
Curator_confirmedWBPerson712
Remark12504/12505-22184/22185 (9680 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