Phenotypes associated with this allele

• Allele Symbol: Cntnap1^tm1Bhat
• Allele Name: targeted mutation 1, Manzoor A Bhat
• Allele ID: MGI:4818635
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cntnap1^tm1Bhat/Cntnap1^tm1Bhat	involves: 129S7/SvEvBrd	MGI:4818644

Genotype
MGI:4818644

hm1

• Allelic Composition: Cntnap1^tm1Bhat/Cntnap1^tm1Bhat
• Genetic Background: involves: 129S7/SvEvBrd

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

mortality/aging

lethality at weaning, incomplete penetrance ( J:107653 )

• phenotype is identical to that reported for Ccr10/Cntnap1^tm1Bhat in J:69621

premature death ( J:107653 )

behavior/neurological

tremors ( J:107653 )

ataxia ( J:107653 )

weakness ( J:107653 )

abnormal gait ( J:107653 )

decreased locomotor activity ( J:107653 )

paresis ( J:107653 )

growth/size/body

decreased body size ( J:107653 )

decreased body weight ( J:107653 )

nervous system

nervous system phenotype ( J:107653 )

N • gross morphology and development of the cerebellum is normal

abnormal axon morphology ( J:107653 )

abnormal myelin sheath morphology ( J:107653 )

hypermyelination ( J:107653 )

abnormal action potential ( J:107653 )

decreased nerve conduction velocity ( J:107653 )

muscle

muscle spasm ( J:107653 )

skeleton

kyphosis ( J:107653 )