Phenotypes associated with this allele

• Allele Symbol: Mitf^mi-x
• Allele Name: microphthalmia x
• Allele ID: MGI:2662152
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Mitf^mi-x/Mitf^mi-x	involves: NZB/Mac	MGI:2663063
ht2	Mitf^Mi-wh/Mitf^mi-x	involves: NZB/Mac	MGI:2663064

Genotype
MGI:2663063

hm1

• Allelic Composition: Mitf^mi-x/Mitf^mi-x
• Genetic Background: involves: NZB/Mac

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

pigmentation

abnormal coat/hair pigmentation ( J:83501 )

• white coat

abnormal eye pigmentation ( J:83501 )

• black eyes

vision/eye

abnormal eye pigmentation ( J:83501 )

• black eyes

integument

abnormal coat/hair pigmentation ( J:83501 )

• white coat

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:83501
Tietz syndrome		DOID:0090002	OMIM:103500	J:83501
Waardenburg syndrome type 2A		DOID:0110950	OMIM:193510	J:83501

Genotype
MGI:2663064

ht2

• Allelic Composition: Mitf^Mi-wh/Mitf^mi-x
• Genetic Background: involves: NZB/Mac

vision/eye

microphthalmia ( J:83501 )

• reduced eye size

abnormal eyelid morphology ( J:83501 )

• eyelid closure is of variable extent

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:83501
Tietz syndrome		DOID:0090002	OMIM:103500	J:83501
Waardenburg syndrome type 2A		DOID:0110950	OMIM:193510	J:83501