Variation Information: tm6395

Nametm6395 View on WormBase
Species C. elegans
Genetic positiongenetic position unknown or not listed
Genomic positionIV: 3118833..3119419
Protein changeY67D8C.10a Y67D8C.10a Y67D8C.10a Y67D8C.10a Y67D8C.10b Y67D8C.10b Y67D8C.10b Y67D8C.10b Y67D8C.10c Y67D8C.10d Y67D8C.10e Deletion

Strains carrying this variation

Strain Genotype Species Description
FX19163 mca-3(tm6395)/tmIn11 IV. C. elegans Homozygous lethal deletion allele balanced by Unc-marked translocation. Heterozygotes are wild-type and segregate wild-type heterozygotes, lethal tm6395 homozygotes, and Unc tmIn11 homozygotes. Break points: In(kvs-5 unc-17) IV. Covered region (Mb) 2.9 (0.7..3.6) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.