Phenotypes for Mitf MGI:2663064 MGI Mouse

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Phenotypes Associated with This Genotype

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

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mitf^Mi-wh mutation (8 available); any Mitf mutation (74 available)
Mitf^mi-x mutation (0 available); any Mitf mutation (74 available)

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

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

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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