Variation Information: n3261

Namen3261 View on WormBase
Species C. elegans
Genetic positionI:4.76 +/- 0.000 cM
Genomic positionI: 10224606..10224606
Protein change Substitution

Strains carrying this variation

Strain Genotype Species Description
MT11068 ced-12(n3261) I. C. elegans Defects in engulfment, persistent cell coprses observed in embyros, larvae, and adult hermaphrodite gonads. Distal tip cell migration defects.