Phenotypes associated with this allele

• Allele Symbol: Alm
• Allele Name: anterior lenticonus with microphthalmia
• Allele ID: MGI:1856649
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Alm/Alm	involves: 101 * C3H	MGI:2175694
ht2	Alm/Alm^+	involves: 101 * C3H	MGI:2175695

Genotype
MGI:2175694

hm1

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

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

mortality/aging

preweaning lethality, complete penetrance ( J:6686 )

Genotype
MGI:2175695

ht2

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

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