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Phenotypes Associated with This Genotype
Genotype
MGI:3587636
Allelic
Composition
Mitfmi-enu122/Mitf+
Genetic
Background
involves: 102 * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mitfmi-enu122 mutation (0 available); any Mitf mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• reduced retinal pigmentation
• iris and coat pigmentation normal and eye size normal

pigmentation
• reduced retinal pigmentation
• iris and coat pigmentation normal and eye size normal

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Waardenburg syndrome type 2A DOID:0110950 OMIM:193510
J:46254


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
06/13/2017
MGI 6.10
The Jackson Laboratory