Phenotypes Associated with This Genotype

Genotype
MGI:4455020

• Allelic Composition: Mitf^mi-ew/Mitf^mi-ew
• Genetic Background: involves: C57BL/6Bn * NAW

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

pigmentation

absent coat pigmentation ( J:89821 )

• white coat

skeleton

exostosis ( J:89821 )

• 3 week old bones show signs of hyperostosis, with extensions of bony trabeculae that reach further into the bone marrow cavity than in wild-type mice

osteopetrosis ( J:89821 )

• mild osteopetrosis

vision/eye

microphthalmia ( J:89821 )

• severely microphthalmic

integument

absent coat pigmentation ( J:89821 )

• white coat

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Camurati-Engelmann disease		DOID:4997	OMIM:131300 OMIM:606631	J:89821