Prmt7^tm1.2Rchd
Targeted Allele Detail

Summary

• Symbol: Prmt7^tm1.2Rchd
• Name: protein arginine N-methyltransferase 7; targeted mutation 1.2, Stephane Richard
• MGI ID: MGI:6281578
• Gene: Prmt7 Location: Chr8:106937686-106978326 bp, + strand Genetic Position: Chr8, 53.11 cM
• Alliance: Prmt7^tm1.2Rchd page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:271361
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: 129/Sv

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: Exon 4 was flanked with loxP and FRT sites. Flp-mediated recombination removed the selection cassette inserted in intron 4. Cre-mediated recombination removed exon 4. (J:271361)

Expression

In Structures Affected by this Mutation:

4 anatomical structure(s)

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 Prmt7 Mutation: 39 strains or lines available

References

• Original: J:271361 Blanc RS, et al., PRMT7 Preserves Satellite Cell Regenerative Capacity. Cell Rep. 2016 Feb 16;14(6):1528-1539
• All: 1 reference(s)