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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pcdhgtm1.2Sch
targeted mutation 1.2, Martin K Schwarz
MGI:5504505
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Pcdhgtm1.2Sch/Pcdhgtm1.2Sch B6.129-Pcdhgtm1.2Sch MGI:5504531


Genotype
MGI:5504531
cn1
Allelic
Composition
Pcdhgtm1.2Sch/Pcdhgtm1.2Sch
Genetic
Background
B6.129-Pcdhgtm1.2Sch
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pcdhgtm1.2Sch mutation (0 available); any Pcdhg mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• a lentivirus construct expressing cre and EGFP is injected into the subventricular zone of neonatal mice. B type stem cells, C type transit amplifying cells, and A type neuroblasts are infected
• abnormal development of infected cells that have migrated to the olfactory bulb by 14 days after infection
• fewer cells reach the olfactory bulb from the subventricular zone
• cells reaching the olfactory bulb have acquired a neuronal identity
• decreased apical dendrite length in granule cells by 42 days after infection
• reduced dendritic branching
• reduced arbor complexity starting at 14 days after infection
• significantly reduced spine number on dendrites of granule cells of the olfactory bulb





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory