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WormBase Tree Display for Variation: WBVar00601202

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Name Class

WBVar00601202NamePublic_namegkDf30
Sequence_detailsSMapS_parentSequenceCHROMOSOME_V
Flanking_sequencesATATCGAGGAACTGCAAAACAAACTTTTTTCGTTGATTTTTCGATTCCTTTTCTTCTTCA
Mapping_targetCHROMOSOME_V
CGH_deleted_probesGTGTGGATTTGATATACAGGCAATCGAAAATACCTGATATCCATAAAATAATTGTCCGCTGGCGTCATCTATGATCGGGCGGTGACCAAACAAGATTTGC
CGH_flanking_probesTGCATTATATACCTTTTAATGTCTTCTCAATATCGAGGAACTGCAAAACACAGATGCTGCGATAACGATCTTACAGTGAATCGGCGCTTAATTAACGAAA
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryVC
PersonWBPerson427
Detection_methodOligo array CGH
StatusLive
AffectsGeneWBGene00006954
WBGene00006953
WBGene00005860
WBGene00044086
WBGene00010355
TranscriptH02K04.2.1
ZK1037.9.1
C29F3.2.1
H02K04.1.1
ZK1037.10.1
IsolationMutagenUV/TMP
GeneticsMapV
RemarkFlanking probes represent the nearest array oligo sequences present in the deletion chromosome on the basis of fluorescence ratio. These should not be considered hard breakpoints in the absence of actual sequence data.
MethodCGH_allele