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Pcnx2C3H/HeJ
Spontaneous Allele Detail
Nomenclature
Symbol: Pcnx2C3H/HeJ
Name: pecanex homolog 2; C3H/HeJ
MGI ID: MGI:6161760
Synonyms: Pcnxl2
Gene: Pcnx2  Location: Chr8:125751508-125898317 bp, - strand  Genetic Position: Chr8, 73.65 cM
Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Insertion
 
Mutation detailsThis IAP insertion in intron 19 causes diminished expression of this gene by RT-PCR in C3H/HeJ and is not found in C3HeB/FeJ, C3H/HeOuJ, or C3H/HeSnJ. (J:228536)
Inheritance:    Not Specified
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Pcnx2 Mutation:  82 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
12/03/2019
MGI 6.14
The Jackson Laboratory