About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Pcnx2em5Frk
endonuclease-mediated mutation 5, Wayne N Frankel
MGI:5818660
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
 		Gria4spkw1/Gria4spkw1
Pcnx2em5Frk/Pcnx2em5Frk 		C3Fe.C3-Pcnx2em5Frk Gria4spkw1 MGI:5818667


Genotype
MGI:5818667
cx1
Allelic
Composition		 Gria4spkw1/Gria4spkw1
Pcnx2em5Frk/Pcnx2em5Frk
Genetic
Background		 C3Fe.C3-Pcnx2em5Frk Gria4spkw1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gria4spkw1 mutation (4 available); any Gria4 mutation (72 available)
Pcnx2em5Frk mutation (0 available); any Pcnx2 mutation (130 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
behavior/neurological
abnormal spike wave discharge ( J:228536 )
• incidence and length of spike wave discharges is decreased as compared to mice homozygous for Gria4spkw1 alone
• incidence and length of spike wave discharges is slightly decreased as compared to C3H/HeJ

nervous system
abnormal spike wave discharge ( J:228536 )
• incidence and length of spike wave discharges is decreased as compared to mice homozygous for Gria4spkw1 alone
• incidence and length of spike wave discharges is slightly decreased as compared to C3H/HeJ




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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory