Variation Information: bx38

Namebx38 View on WormBase
Species C. elegans
Genetic positionX:-2.80 +/- 0.594 cM
Genomic positiongenomic coordinates unknown or not listed
Protein changeprotein change unknown or not listed

Strains carrying this variation

Strain Genotype Species Description
EM111 him-5(e1490) V; mab-19(bx38) X. C. elegans Male phenotype: loss of rays 7-9; incomplete penetrance/expressivity (80%); T lineage defect. Hermaphrodite phenotype: lowered brood size (100 progeny/hermaphrodite). Hypomorphic allele: uDf1/mab-19(bx38) results in embryonic arrest during morphogenesis.