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WormBase Tree Display for Variation: WBVar02153446

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Name Class

WBVar02153446NamePublic_namerh311
Sequence_detailsSeqStatusPending_curation
OriginSpeciesCaenorhabditis elegans
StatusLive
Possibly_affectsWBGene00000674Paper_evidenceWBPaper00053867
RemarkCGC_name col-99
DescriptionPhenotypeWBPhenotype:0000515Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
Remarkcol-99 mutants exhibit guidance defects in axons extending along the major longitudinal axon tracts, most prominently the left ventral nerve cord (VNC).Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
WBPhenotype:0001224Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
Remarkcol-99 mutants exhibit guidance defects in axons extending along the major longitudinal axon tracts, most prominently the left ventral nerve cord (VNC).Paper_evidenceWBPaper00053867
Curator_confirmedWBPerson557
ReferenceWBPaper00053867
Remark[2021-06-01T18:38:31.546Z WBPerson2987] New Variation: WBPaper00053867; allele of col-99; Sequencing of the coding region of col-99b in rh311 revealed a G to A transition that disrupts the splice donor site at the beginning of intron 13.Curator_confirmedWBPerson2987
MethodAllele