Phenotypes associated with this allele

• Allele Symbol: lg^Stn
• Allele Name: lid gap Stein
• Allele ID: MGI:1857109
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	lg^Stn/lg^Stn	Not Specified	MGI:5320578

Genotype
MGI:5320578

hm1

• Allelic Composition: lg^Stn/lg^Stn
• Genetic Background: Not Specified

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

vision/eye

abnormal cornea morphology ( J:5166 )

• corneal disorganization observed in histologicval sections of newborn

abnormal eye development ( J:5166 , J:7160 , J:7495 , J:8009 )

• Background Sensitivity: one or both eyes (J:5166)

• in overall severity, alleles rank in the order lg > lg^Stn = lg^St > lg^Ga > lg^Ml (J:7160)

• administration of cortisone to the mother on E14 of pregnancy normalizes eye development in offspring (J:7495)

• thyroxine administered to the mother at E10-E11 of gestation normalizes eye development in offspring (J:8009)

lens vacuoles ( J:5166 )

• detectable at E14-16, extensive at E17

eyelids open at birth ( J:5056 )

• Background Sensitivity: one or both eyes are open at birth, with a 70-100 percent incidence of at least one eye affected depending on genetic background

abnormal retina morphology ( J:5166 )

• detected in histological analysis of 2 day old pups