This phenotypic mutant was identified in an ENU mutagenesis screen at the Baylor College of Medicine. The original line contains two mutations: Myh10ehc and an unmapped mutation between D11MIT322 and D11MIT35. (J:248868)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count