Pacsin1^em1(IMPC)H
Endonuclease-mediated Allele Detail

Summary

• Symbol: Pacsin1^em1(IMPC)H
• Name: protein kinase C and casein kinase substrate in neurons 1; endonuclease-mediated mutation 1, Harwell
• MGI ID: MGI:6402889
• Gene: Pacsin1 Location: Chr17:27874565-27930092 bp, + strand Genetic Position: Chr17, 14.59 cM, cytoband B1
• Alliance: Pacsin1^em1(IMPC)H page
• IMPC: Pacsin1 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 CCACAGGGCGTACATTGGAAAGG, CCTGTGACTGGCATGTCTGCAGT, CCCAAATGAGCCCAGGGACTGGA, ATGCTGGAGAAGAACCCATAGGG, which resulted in a Exon Deletion. (J:265051)
• Inheritance: Not Specified

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

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 Pacsin1 Mutation: 30 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: 3 reference(s)