Phenotypes Associated with This Genotype

Genotype
MGI:2668608

• Allelic Composition: Slc45a2^uw-d/Slc45a2^uw-d
• Genetic Background: involves: TF/Le

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

pigmentation

irregular coat pigmentation ( J:41299 )

• reduced pigmentation, the ventrun of homozygous mutants are lighter than the dorsum

abnormal eye pigmentation ( J:41299 )

• eyes are light at birth but darken with age; adult eye is a deep, dark ruby, although it may appear black to the untrained observer

vision/eye

abnormal eye pigmentation ( J:41299 )

• eyes are light at birth but darken with age; adult eye is a deep, dark ruby, although it may appear black to the untrained observer

integument

irregular coat pigmentation ( J:41299 )

• reduced pigmentation, the ventrun of homozygous mutants are lighter than the dorsum

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
oculocutaneous albinism		DOID:0050632	OMIM:PS203100	J:41299