Phenotypes Associated with This Genotype

Genotype
MGI:3587636

• Allelic Composition: Mitf^mi-enu122/Mitf⁺
• Genetic Background: involves: 102 * C3H

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

vision/eye

abnormal retina pigmentation ( J:46254 )

• reduced retinal pigmentation

• iris and coat pigmentation normal and eye size normal

pigmentation

abnormal retina pigmentation ( J:46254 )

• reduced retinal pigmentation

• iris and coat pigmentation normal and eye size normal

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:46254
Tietz syndrome		DOID:0090002	OMIM:103500	J:46254
Waardenburg syndrome type 2A		DOID:0110950	OMIM:193510	J:46254