Phenotypes Associated with This Genotype

Genotype
MGI:2686995

• Allelic Composition: Mitf^Mi-H/Mitf⁺
• Genetic Background: involves: BALB/cAnN * C3H/HeN

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

pigmentation

decreased ear pigmentation ( J:75964 )

• mice were described as having pale ears

abnormal coat/hair pigmentation ( J:75964 )

irregular coat pigmentation ( J:75964 )

• described as having pale patches on their coats, most often as a head or belly spot

abnormal foot pigmentation ( J:75964 )

• mice were described as having pale feet

decreased tail pigmentation ( J:75964 )

• mice were described as having pale tails

hearing/vestibular/ear

decreased ear pigmentation ( J:75964 )

• mice were described as having pale ears

limbs/digits/tail

decreased tail pigmentation ( J:75964 )

• mice were described as having pale tails

vision/eye

abnormal iris morphology ( J:75964 )

• eye examination showed mild iris transillumination

craniofacial

decreased ear pigmentation ( J:75964 )

• mice were described as having pale ears

integument

decreased ear pigmentation ( J:75964 )

• mice were described as having pale ears

abnormal coat/hair pigmentation ( J:75964 )

irregular coat pigmentation ( J:75964 )

• described as having pale patches on their coats, most often as a head or belly spot

abnormal foot pigmentation ( J:75964 )

• mice were described as having pale feet

decreased tail pigmentation ( J:75964 )

• mice were described as having pale tails

growth/size/body

decreased ear pigmentation ( J:75964 )

• mice were described as having pale ears

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:75964
Tietz syndrome		DOID:0090002	OMIM:103500	J:75964
Waardenburg syndrome type 2A		DOID:0110950	OMIM:193510	J:75964