Pcnx2^C3H/HeJ
Spontaneous Allele Detail

Summary

• Symbol: Pcnx2^C3H/HeJ
• Name: pecanex homolog 2; C3H/HeJ
• MGI ID: MGI:6161760
• Synonyms: Pcnxl2^IAP
• Gene: Pcnx2 Location: Chr8:126478247-126625056 bp, - strand Genetic Position: Chr8, 73.65 cM
• Alliance: Pcnx2^C3H/HeJ page

Mutation origin

• Strain of Origin: C3H/HeJ

Mutation description

• Allele Type: Spontaneous (Hypomorph)
• Mutation: Insertion
• Mutation details: This 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: 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)