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Plin2em1Tcp
Endonuclease-mediated Allele Detail
Summary
Symbol: Plin2em1Tcp
Name: perilipin 2; endonuclease-mediated mutation 1, The Centre for Phenogenomics
MGI ID: MGI:7489806
Gene: Plin2  Location: Chr4:86566623-86588297 bp, - strand  Genetic Position: Chr4, 40.69 cM
Alliance: Plin2em1Tcp page
Mutation
origin
Strain of Origin:  C57BL/6NCrl
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Nucleotide substitutions
 
Mutation detailsThis knockin allele was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with guide RNAs with the spacer sequences AGCAGTAGTGGATCCGCAAC. The Rosella fluorescent pH-biosensor ORF was delivered by AAV transduction and was inserted between 86586916 and 86586917 of Chr4 (GRCm39). Silent mutations were introduced in Plin2 at c.15 A>C (p.Val5), c.21 T>C(p.AspD7), and c.24 G>T (p.Pro8). (J:200814)
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 Plin2 Mutation:  40 strains or lines available
References
Original:  J:200814 Toronto Centre for Phenogenomics, Strains and alleles submitted by Toronto Centre for Phenogenomics (NorCOMM2, funded by Genome Canada and Ontario Genomics Institute OGI-051). MGI Direct Data Submission. 2013;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/12/2026
MGI 6.24
The Jackson Laboratory