This phenotypic mutant was identified in an ENU mutagenesis screen at the Baylor College of Medicine. A complementation test with Tyrc-ch mice demonstrated that this mutation is an allele of the Tyr gene.
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count