Mouse Genome Informatics
hm
    MitfMi-Crc/MitfMi-Crc
CBA/CaCrc
Key:
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• hairs have no pigment
• eyes show no pigment

craniofacial

reproductive system

skeleton

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

integument
• hairs have no pigment

growth/size/body

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