Mouse Genome Informatics
hm
    Mitfmi-enu122/Mitfmi-enu122
involves: 102 * C3H
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       

Mitfmi-enu122/Mitfmi-enu122 mouse

vision/eye
• severely reduced eye pigmentation (J:46254)
• pink eyes (J:63651)
• some reduction in the size of the eyes

pigmentation
• mostly white with diffuse, faintly pigmented patches in coat
• severely reduced eye pigmentation (J:46254)
• pink eyes (J:63651)

limbs/digits/tail

integument
• mostly white with diffuse, faintly pigmented patches in coat

Mouse Models of Human Disease
OMIM IDRef(s)
Albinism, Ocular, with Sensorineural Deafness 103470 J:46254
Tietz Syndrome 103500 J:46254
Waardenburg Syndrome, Type 2A; WS2A 193510 J:46254