Mylip^{tm1.1(KOMP)Vlcg}
Targeted Allele Detail

Summary

• Symbol: Mylip^{tm1.1(KOMP)Vlcg}
• Name: myosin regulatory light chain interacting protein; targeted mutation 1.1, Velocigene
• MGI ID: MGI:5576056
• Gene: Mylip Location: Chr13:45543218-45565498 bp, + strand Genetic Position: Chr13, 21.88 cM
• Alliance: Mylip^{tm1.1(KOMP)Vlcg} page
• IMPC: Mylip gene page

Mutation origin

• Mutant Cell Line: 17270C-G8
• Germline Transmission: Earliest citation of germline transmission: J:188991
• Parent Cell Line: VGB6 (ES Cell)
• Strain of Origin: C57BL/6NTac
• Project Collection: KOMP-Regeneron

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion Vector: ZEN-Ub1
• Mutation details: The insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 20639bp between positions 45485238-45505876 of Chromosome 13 (Genome Build37), and subsequent Cre-mediated excision deleted the neomycin selection cassette. (J:136110, J:188991)

Expression

In Mice Carrying this Mutation:	46 assay results
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: 1 strain available Cell Lines: 0 lines available
• Carrying any Mylip Mutation: 23 strains or lines available

References

• Original: J:188991 The Jackson Laboratory, Alleles produced for the KOMP project by The Jackson Laboratory. MGI Direct Data Submission. 2012
• All: 5 reference(s)