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Nsmftm1.2Mrkr
Targeted Allele Detail
Summary
Symbol: Nsmftm1.2Mrkr
Name: NMDA receptor synaptonuclear signaling and neuronal migration factor; targeted mutation 1.2, Michael R Kreutz
MGI ID: MGI:6358416
Gene: Nsmf  Location: Chr2:24944370-24952893 bp, + strand  Genetic Position: Chr2, 16.94 cM, cytoband A3
Alliance: Nsmftm1.2Mrkr page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:232404
Parent Cell Line:  Bruce 4 (ES Cell)
Strain of Origin:  B6.Cg-Thy1a
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA loxP site was inserted into the 5UTR of exon 1, an FRT-flanked PGK-neomycin selection cassette was inserted after exon 2, followed by a loxP site and a third loxP site downstream of exon 3. Flp-mediated recombination removed the selection cassette and cre-mediated recombination deleted exons 1-3. Western blot analysis confirmed absence of protein. (J:232404)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 6 anatomical structure(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 Nsmf Mutation:  18 strains or lines available
References
Original:  J:232404 Spilker C, et al., A Jacob/Nsmf Gene Knockout Results in Hippocampal Dysplasia and Impaired BDNF Signaling in Dendritogenesis. PLoS Genet. 2016 Mar;12(3):e1005907
All:  2 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
11/05/2024
MGI 6.24
The Jackson Laboratory