Variation Information: vs137

Namevs137 View on WormBase
Species C. elegans
Genetic positionIV:3.32 +/- 0.000 cM
Genomic positionIV: 7330228..7330915
Protein changeY40C5A.2 Deletion

Strains carrying this variation

Strain Genotype Species Description
LX950 ocr-4(vs137) IV. C. elegans Phenotypically WT. Deletion allele. A "T" is added also. The end points of the deletion are: TCGAACGTCAACAACATATTGCAAAT.....t.....TTGGAAAGGTAGGCTTACACTT TTTTTAA.
LX980 ocr-4(vs137) IV; ocr-1(ok132) V. C. elegans vs137 is a deletion allele. A "T" has been added. The endpoints of the deletion are: TCGAACGTCAACAACATATTGCAAAT.......T.......TTGGAAAGGTAGGCTTAC ACTTTTTTTAA. Double mutants have reduced AWA gene expression. ok132 is a deletion and putative null allele. The boundaries of the deletion are: AGATTACTGATGCCATTGAACAAGTTCTCGTCA......TGATGTTTGAAAGGTGGAGT AGCAAAGAGA.
LX981 ocr-4(vs137) ocr-2(ak47) IV. C. elegans ak47 is chemosensory, mechanosensory and osmosensory defective, and is a null allele. vs137 is a deletion allele. A "T" has been added. The endpoints of the deletion are: TCGAACGTCAACAACATATTGCAAAT.......T.......TTGGAAAGGTAGGCTTAC ACTTTTTTTAA.
LX982 ocr-4(vs137) ocr-2(ak47) IV; ocr-1(ok132) V. C. elegans Chemosensory, mechanosensory, and osmosensory defects.