Phenotypes Associated with This Genotype

Genotype
MGI:2662939

• Allelic Composition: Mitf^Mi-Crc/Mitf^Mi-Crc
• Genetic Background: involves: CBA/CaCrc

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

pigmentation

absent coat pigmentation ( J:83500 )

• hairs have no pigment

decreased eye pigmentation ( J:83500 )

• eyes show no pigment

craniofacial

failure of tooth eruption ( J:83500 )

reproductive system

female infertility ( J:83500 )

♀

male infertility ( J:83500 )

♂

skeleton

failure of tooth eruption ( J:83500 )

osteopetrosis ( J:83500 )

vision/eye

decreased eye pigmentation ( J:83500 )

• eyes show no pigment

microphthalmia ( J:83500 )

eyelids fail to open ( J:83500 )

• eyelids do not open

integument

absent coat pigmentation ( J:83500 )

• hairs have no pigment

growth/size/body

failure of tooth eruption ( J:83500 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
ocular albinism with sensorineural deafness		DOID:0090100		J:83500
Tietz syndrome		DOID:0090002	OMIM:103500	J:83500
Waardenburg syndrome type 2A		DOID:0110950	OMIM:193510	J:83500