Snx14^em1(IMPC)H
Endonuclease-mediated Allele Detail

Summary

• Symbol: Snx14^em1(IMPC)H
• Name: sorting nexin 14; endonuclease-mediated mutation 1, Harwell
• MGI ID: MGI:6153823
• Gene: Snx14 Location: Chr9:88258805-88320982 bp, - strand Genetic Position: Chr9, 47.24 cM
• Alliance: Snx14^em1(IMPC)H page
• IMPC: Snx14 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 from IMPC was generated at Medical Research Council Harwell by injecting CAS9 RNA and 4 guide sequences CCCCGAATGGACTACTCTGCGAT, CCGAATGGACTACTCTGCGATAC, GTAGAAAGTGTAGCCGGGCGTGG, CTTTAATCCCAACACTCGGGAGG, which resulted in a deletion of 571nucleotides flanking exon 3. (J:237616, J:294712)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Snx14 Mutation: 52 strains or lines available

References

• Original: J:237616 MGI and IMPC, MGI Curation of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC). MGI Direct Data Submission. 2017-8
• All: 4 reference(s)