Variation Information: n4871

Namen4871 View on WormBase
Species C. elegans
Genetic positionIV:3.15 +/- 0.003 cM
Genomic positiongenomic coordinates unknown or not listed
Protein changeprotein change unknown or not listed

Strains carrying this variation

Strain Genotype Species Description
MT15883 csp-2(n4871) IV. C elegans n4871 is a 1136 bp deletion that removes the last five exons, including the putative protease active site. Reference: Denning DP, et al. PLoS Genet. 2013;9(3):e1003341.