Phenotypes Associated with This Genotype

Genotype
MGI:2686998

• Allelic Composition: Mitf^Rorp/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 a slightly paler ears

abnormal coat/hair pigmentation ( J:75964 )

diluted coat color ( J:75964 )

• mice were described as having a slightly paler coat than wild-type

decreased tail pigmentation ( J:75964 )

• mice were described as having a slightly paler tails

hearing/vestibular/ear

decreased ear pigmentation ( J:75964 )

• mice were described as having a slightly paler ears

limbs/digits/tail

decreased tail pigmentation ( J:75964 )

• mice were described as having a slightly paler tails

vision/eye

abnormal retina morphology ( J:75964 )

• patches of orange were noted on the retina

craniofacial

decreased ear pigmentation ( J:75964 )

• mice were described as having a slightly paler ears

integument

decreased ear pigmentation ( J:75964 )

• mice were described as having a slightly paler ears

abnormal coat/hair pigmentation ( J:75964 )

diluted coat color ( J:75964 )

• mice were described as having a slightly paler coat than wild-type

decreased tail pigmentation ( J:75964 )

• mice were described as having a slightly paler tails

growth/size/body

decreased ear pigmentation ( J:75964 )

• mice were described as having a slightly paler 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