Mouse Genome Informatics
ht
    MitfMi-wh/Mitf+
involves: C57BL * DBA
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       

MitfMi-wh/+

pigmentation
• coat color is gray and somewhat lighter than that of Myo5ad homozygotes (J:13058)
• coat color darkens slightly with age (J:13058)
• small spots may occur on the back, but spotting is not found on the head
• reduced foot pigmentation
• reduced tail pigmentation
• moderate dilution of the iris pigmentation
• eyes are a very dark ruby color

limbs/digits/tail
• reduced tail pigmentation

vision/eye
• moderate dilution of the iris pigmentation
• eyes are a very dark ruby color

integument
• coat color is gray and somewhat lighter than that of Myo5ad homozygotes (J:13058)
• coat color darkens slightly with age (J:13058)
• small spots may occur on the back, but spotting is not found on the head
• reduced foot pigmentation
• reduced tail pigmentation

Mouse Models of Human Disease
OMIM IDRef(s)
Albinism, Ocular, with Sensorineural Deafness 103470 J:13058
Tietz Syndrome 103500 J:13058
Waardenburg Syndrome, Type 2A; WS2A 193510 J:13058