Lonrf2^em1(IMPC)H
Endonuclease-mediated Allele Detail

Summary

• Symbol: Lonrf2^em1(IMPC)H
• Name: LON peptidase N-terminal domain and ring finger 2; endonuclease-mediated mutation 1, Harwell
• MGI ID: MGI:6302757
• Gene: Lonrf2 Location: Chr1:38832750-38875768 bp, - strand Genetic Position: Chr1, 17.17 cM
• Alliance: Lonrf2^em1(IMPC)H page
• IMPC: Lonrf2 gene page

Mutation origin

• Strain of Origin: C57BL/6NTac
• Project Collection: IMPC

Mutation description

• Allele Type: Endonuclease-mediated (Null/knockout)
• Mutation: Intragenic deletion
• Mutation details: This allele was generated at Medical Research Council Harwell using Cas9 and 4 guides with spacer sequences AAAAAGAGAGCCGGCATGGT and GATCAAGTTGGTACACATTC that targeted exon(s) ENSMUSE00000603482.2. This resulted in deletion(s) of 611 bp (location: Chr1:38851931-38852541; GRCm39). This description was generated automatically. Additional molecular information including FASTA sequence support for this allele can be found here: (IMPC Gene page) and viewed in a genome context here: (IMPC Genome Browser). (J:384794)

• Inheritance: Not Specified

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 Lonrf2 Mutation: 44 strains or lines available

References

• Original: J:265051 MGI and IMPC, MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC). Database Release. 2018-2023
• All: 2 reference(s)