Variation Information: n4827

Strains carrying this variation

Strain	Genotype	Species	Description
MT22914	gcn-1(n4827) III.	C elegans	n4827 is a null allele of gcn-1 and that loss of gcn-1 function causes a defect in M4 sister cell death. Reference: Hirose T & Horvitz HR. PLoS Genet. 2014 Aug 7;10(8):e1004512.