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Grntm1.2Pvd
Targeted Allele Detail
Summary
Symbol: Grntm1.2Pvd
Name: granulin; targeted mutation 1.2, Philip Van Damme
MGI ID: MGI:6116381
Gene: Grn  Location: Chr11:102321333-102327635 bp, + strand  Genetic Position: Chr11, 66.29 cM
Alliance: Grntm1.2Pvd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:243041
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsAn FRT-flanked selection cassette with a 3' loxP site was inserted upstream of exon 2. An additional loxP site was inserted downstream of exon 8. Flp-mediated recombination removed the selection cassette and left exons 2 through 8 floxed. Cre-mediated recombination removed exons 2 through 8. ELISA confirmed the absence of protein expression in brain and spinal cords. (J:243041)
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 Grn Mutation:  51 strains or lines available
References
Original:  J:243041 Beel S, et al., Progranulin functions as a cathepsin D chaperone to stimulate axonal outgrowth in vivo. Hum Mol Genet. 2017 Aug 1;26(15):2850-2863
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
12/30/2025
MGI 6.24
The Jackson Laboratory