A new allelic series at the underwhite gene is described. Three of the alle
les in the series-uw, uw(d), and Uw(dbr)-arose as spontaneous mutations on
different genetic backgrounds at The Jackson Laboratory. We report here the
visible phenotypes and dominance hierarchy of these alleles, all of which
are defined by a reduction of pigmentation in both eye and coat color. Elec
tron microscopic analysis of retinal epithelium suggests that the primary d
efect is in the melanosome. The degree of severity of melanosome anomalies
in the retina correlates with the degree or hypopigmentation in the coat. T
he perturbed gene and its gene product are unknown. We show that the uw loc
us is genetically distinct from Myo10, a suggested candidate gene for this
mutation.