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Phenotypes Associated with This Genotype
Genotype
MGI:3802492
Allelic
Composition		 Pcntm239Asp/Pcntm239Asp
Tg(Rr291-lacZ)#Mekk/0
Genetic
Background		 involves: C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pcntm239Asp mutation (0 available); any Pcnt mutation (159 available)
Tg(Rr291-lacZ)#Mekk mutation (0 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
nervous system
abnormal cerebral cortex morphology ( J:136795 )
• at E14.5, mice exhibit abnormal interneuron migration in the cerebral cortex
• the crispness of the boundary between the subventricular zone and the stream of migrating cells is lost

limbs/digits/tail
polydactyly ( J:136795 )
• anterior

Contributing Projects:
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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Send questions and comments to User Support. 		last database update
05/28/2024
MGI 6.13 		The Jackson Laboratory