Phenotypes Associated with This Genotype

Genotype
MGI:2662973

• Allelic Composition: Mitf^Mi-Crc/Mitf⁺
• Genetic Background: involves: CBA/CaCrc

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

pigmentation

variable body spotting ( J:83500 )

• some heterozygotes show white spotting on the belly but not on the head

non-pigmented tail tip ( J:83500 )

abnormal iris pigmentation ( J:83500 )

• iris pigment is reduced

limbs/digits/tail

non-pigmented tail tip ( J:83500 )

vision/eye

abnormal iris pigmentation ( J:83500 )

• iris pigment is reduced

integument

variable body spotting ( J:83500 )

• some heterozygotes show white spotting on the belly but not on the head

non-pigmented tail tip ( J:83500 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:83500
Tietz syndrome		DOID:0090002	OMIM:103500	J:83500
Waardenburg syndrome type 1		DOID:0110948	OMIM:193500	J:83500