Phenotypes associated with this allele

• Allele Symbol: Del(5Letm1-Htt)1Jcs
• Allele Name: deletion, Chr 5, John C Schimenti 1
• Allele ID: MGI:3798071
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Del(5Letm1-Htt)1Jcs/+	involves: 129S4/SvJae * C57BL/6J	MGI:3798200

Genotype
MGI:3798200

ht1

• Allelic Composition: Del(5Letm1-Htt)1Jcs/+
• Genetic Background: involves: 129S4/SvJae * C57BL/6J

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

behavior/neurological

convulsive seizures ( J:67077 )

• spontaneous convulsive seizure episodes occassionally occur but heterozygotes do not have an increased incidence of high frequency electrically induced seizures

nervous system

convulsive seizures ( J:67077 )

• spontaneous convulsive seizure episodes occassionally occur but heterozygotes do not have an increased incidence of high frequency electrically induced seizures

abnormal cerebellar foliation ( J:67077 )

abnormal corpora quadrigemina morphology ( J:67077 )

abnormal cerebral cortex morphology ( J:67077 )

• hypoplasia of the cerebral cortex results in colliculi being more exposed, although lobulation defects, which are found in other deletions in this region, are not observed

vision/eye

vision/eye phenotype ( J:67077 )

N • no ocular defects found