Phenotypes Associated with This Genotype

Genotype
MGI:2175077

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

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

mortality/aging

premature death ( J:6686 )

• high mortality

vision/eye

abnormal pupillary reflex ( J:6686 )

• pupillary reaction is absent

blepharitis ( J:6686 )

• inflammation of eyelids

abnormal iris morphology ( J:9528 )

• dysplasia

abnormal pupil morphology ( J:6686 )

• irregularly shaped

corneal opacity ( J:6686 , J:9528 )

abnormal lens morphology ( J:9528 )

• lens dysplasia

fused cornea and lens ( J:6686 )

cataract ( J:6686 )

• bilateral

total cataract ( J:9528 )

• total opacity

lenticonus ( J:9528 )

microphthalmia ( J:6686 , J:9528 )

growth/size/body

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

pigmentation

belly spot ( J:6686 , J:9528 )

immune system

blepharitis ( J:6686 )

• inflammation of eyelids

behavior/neurological

abnormal pupillary reflex ( J:6686 )

• pupillary reaction is absent

integument

belly spot ( J:6686 , J:9528 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
cataract		DOID:83	OMIM:601371 OMIM:PS116200	J:9528