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Phenotypes Associated with This Genotype
Genotype
MGI:4455020
Allelic
Composition
Mitfmi-ew/Mitfmi-ew
Genetic
Background
involves: C57BL/6Bn * NAW
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mitfmi-ew mutation (1 available); any Mitf mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation

skeleton
• 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
• mild osteopetrosis

vision/eye
• severely microphthalmic

integument

Mouse Models of Human Disease
OMIM ID Ref(s)
Camurati-Engelmann Disease; CAEND 131300 J:89821


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/12/2016
MGI 6.04
The Jackson Laboratory