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Pcnx2em5Frk
Endonuclease-mediated Allele Detail
Summary
Symbol: Pcnx2em5Frk
Name: pecanex homolog 2; endonuclease-mediated mutation 5, Wayne N Frankel
MGI ID: MGI:5818660
Synonyms: A-11, FS1
Gene: Pcnx2  Location: Chr8:126478247-126625056 bp, - strand  Genetic Position: Chr8, 73.65 cM
Alliance: Pcnx2em5Frk page
Mutation
origin
Strain of Origin:  C3Fe.C3-Gria4spkw1/Frk
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsTALEN mediated recombination produced an 11 bp deletion in exon 16 resulting in a frameshift and premature stop codon. (J:228536)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Pcnx2 Mutation:  130 strains or lines available
References
Original:  J:228536 Frankel WN, et al., Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy. PLoS Genet. 2014 Jul;10(7):e1004454
All:  1 reference(s)

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory