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Mir137tm1.1Penj
Targeted Allele Detail
Summary
Symbol: Mir137tm1.1Penj
Name: microRNA 137; targeted mutation 1.1, Peng Jin
MGI ID: MGI:6282027
Synonyms: Mir137-
Gene: Mir137  Location: Chr3:118227506-118227578 bp, + strand  Genetic Position: Chr3, 51.71 cM
Alliance: Mir137tm1.1Penj page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:271669
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA loxP site was inserted upstream of the gene and an FRT site flanked neomycin resistance gene cassette and a second loxP site were inserted downstream. The gene and selection cassette were deleted in the germline through cre-mediated recombination by crossing mice carying the floxed allele with Zp3-cre allele carying mice. This creates a knockout allele. (J:271669)
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
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 Mir137 Mutation:  5 strains or lines available
References
Original:  J:271669 Cheng Y, et al., Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a. Nat Neurosci. 2018 Dec;21(12):1689-1703
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