Mouse Genome Informatics
hm
    MitfMi-Crc/MitfMi-Crc
CBA/CaCrc
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       
pigmentation
• hairs have no pigment
• eyes show no pigment

craniofacial

reproductive system
(J:83500)

skeleton

vision/eye
• eyes show no pigment
• eyelids do not open

integument
• hairs have no pigment

Mouse Models of Human Disease
OMIM IDRef(s)
Albinism, Ocular, with Sensorineural Deafness 103470 J:83500
Tietz Syndrome 103500 J:83500
Waardenburg Syndrome, Type 2A; WS2A 193510 J:83500