Table 1.

The new mutation (nm) is allelic to sph, sph2BC, and sphJ mutations

Complementation cross (×)*No. mutants†/No. in litter
nm/+ ×sph/+ 2/8  
nm/+ ×sph2BC/+ 2/6  
nm/+ ×sphJ/+ 1/6  
nm/+ ×ja/+ 0/7  
nm/+ ×ja/+ 0/5 
Complementation cross (×)*No. mutants†/No. in litter
nm/+ ×sph/+ 2/8  
nm/+ ×sph2BC/+ 2/6  
nm/+ ×sphJ/+ 1/6  
nm/+ ×ja/+ 0/7  
nm/+ ×ja/+ 0/5 
*

Genotype of female indicated first, genotype of male second.

†

Mutants are identified by their neonatal jaundice.

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