Phenotypes associated with this allele

• Allele Symbol: Pcdh9⁺
• Allele Name: wild type
• Allele ID: MGI:2436800
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Pcdh9^tm1Mjhk/Pcdh9^+	B6.Cg-Pcdh9^tm1Mjhk	MGI:5825247
ht2	Pcdh9^tm1.1(KOMP)Vlcg/Pcdh9^+	C57BL/6N-Pcdh9^tm1.1(KOMP)Vlcg/J	MGI:6263110

Genotype
MGI:5825247

ht1

• Allelic Composition: Pcdh9^tm1Mjhk/Pcdh9⁺
• Genetic Background: B6.Cg-Pcdh9^tm1Mjhk

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

behavior/neurological

behavior/neurological phenotype ( J:237757 )

N • mice exhibit normal novel object recognition after short- or long-term intertrial intervals

abnormal social recognition ( J:237757 )

• following long-term intertrial intervals (ITI), mice exhibit impaired social recognition (SRE) compared with wild-type mice

• however, SRE is normal following a short-term ITI

nervous system

nervous system phenotype ( J:237757 )

N • mice exhibit normal motor cortex layer thickness and cell number

thin cerebral cortex ( J:237757 )

• in deeper layers

abnormal dendrite morphology ( J:237757 )

• mice exhibit reduced total apical dendrite length, surface and number of intersections compared with wild-type mice

decreased neuron number ( J:237757 )

• in deeper layers of the cortex

Genotype
MGI:6263110

ht2

• Allelic Composition: Pcdh9^{tm1.1(KOMP)Vlcg}/Pcdh9⁺
• Genetic Background: C57BL/6N-Pcdh9^{tm1.1(KOMP)Vlcg}/J
• Cell Lines: 16712A-A8

Data Sources

IMPC Data for Pcdh9

behavior/neurological

decreased grip strength ( J:211773 )

IMPC - JAX

hyperactivity ( J:211773 )

IMPC - JAX

increased vertical activity ( J:211773 )

IMPC - JAX

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

IMPC - JAX

increased circulating phosphate level ( J:211773 )

IMPC - JAX

increased circulating aspartate transaminase level ( J:211773 )

♂

IMPC - JAX