Phenotypes Associated with This Genotype

Genotype
MGI:2175695

• Allelic Composition: Alm/Alm⁺
• Genetic Background: involves: 101 * C3H

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

pigmentation

belly spot ( J:6686 , J:9528 )

• white belly spot (J:6686)

• lens dysplasia (J:6686)

growth/size/body

decreased body size ( J:6686 , J:9528 )

reproductive system

infertility ( J:6686 )

• heterozygotes are frequently sterile

vision/eye

abnormal iris morphology ( J:9528 )

• dysplasia

corneal opacity ( J:6686 , J:9528 )

abnormal lens morphology ( J:6686 , J:9528 )

• abnormal lens shape (J:6686)

• dysplasia (J:9528)

fused cornea and lens ( J:6686 )

cataract ( J:6686 )

• anterior opacity

total cataract ( J:9528 )

• total opacity

lenticonus ( J:6686 , J:9528 )

• protruding anterior surface of the lens (J:6686)

microphthalmia ( J:6686 , J:9528 )

integument

belly spot ( J:6686 , J:9528 )

• white belly spot (J:6686)

• lens dysplasia (J:6686)

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
cataract		DOID:83	OMIM:601371 OMIM:PS116200	J:6686