hm1

Mitf^mi-x/Mitf^mi-x
NZB/Mac

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	Euro	Europhenome
N	normal phenotype

pigmentation

abnormal coat/hair pigmentation ( J:83501 )

• white coat

abnormal eye pigmentation ( J:83501 )

• black eyes

vision/eye

abnormal eye pigmentation ( J:83501 )

• black eyes

integument

abnormal coat/hair pigmentation ( J:83501 )

• white coat

Mouse Models of Human Disease		OMIM ID	Ref(s)
Albinism, Ocular, with Sensorineural Deafness		103470	J:83501
Tietz Syndrome		103500	J:83501
Waardenburg Syndrome, Type 2A; WS2A		193510	J:83501

ht2

Mitf^Mi-wh/Mitf^mi-x
NZB/Mac

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	Euro	Europhenome
N	normal phenotype

vision/eye

microphthalmia ( J:83501 )

• reduced eye size

abnormal eyelid morphology ( J:83501 )

• eyelid closure is of variable extent

Mouse Models of Human Disease		OMIM ID	Ref(s)
Albinism, Ocular, with Sensorineural Deafness		103470	J:83501
Tietz Syndrome		103500	J:83501
Waardenburg Syndrome, Type 2A; WS2A		193510	J:83501