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Nlgn3tm4Sud
Targeted Allele Detail
Summary
Symbol: Nlgn3tm4Sud
Name: neuroligin 3; targeted mutation 4, Thomas C Sudhof
MGI ID: MGI:5503959
Synonyms: Nlgn3tm4(Venus)Sud, RB1
Gene: Nlgn3  Location: ChrX:100342785-100364956 bp, + strand  Genetic Position: ChrX, 43.95 cM
Alliance: Nlgn3tm4Sud page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:214636
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Conditional ready, Inserted expressed sequence, Reporter)
Mutation:    Insertion
 
Nlgn3tm4Sud expresses 1 gene
 
Mutation detailsThe following elements were inserted into intron 1: an FRT site, a duplicate of the 3' end of intron 1 and 5' end of the ATG translation start site-containing exon 2, a full-length rat Nlgn3 cDNA (incorporating mutations (L399A, N400A, D402N, E297A, and K306A) that abolish neurexin binding in paralog Nlg1) fused at codon 780 to the monomeric green fluorescent protein mVenus gene, a splice donor site, an F3 FRT site, a neomycin resistance gene cassette, a tandem FRT/F3 FRT site, and a loxP511 site. A second loxP511 site was inserted into intron 3 to allow for conditional cre-mediated deletion of exons 2 and 3. This allele expresses the mutated Nlgn3-mVenus chimeric protein, with the reporter peptide attached to the cytoplasmic side of the Nlgn3 peptide. If this allele is subjected to flp-mediated recombination, two derivative alleles will be produced: a knockin allele without the neo cassette (recombined via the F3 FRT sites), and a conditional knockout (with the neo cassette and knockin transcript removed) expressing the wild-type peptide (recombined via the FRT sites). qRT-PCR reveals decreased expression levels of the knockin transcript compared to the wild-type. (J:214636)
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 Nlgn3 Mutation:  35 strains or lines available
References
Original:  J:214636 Rothwell PE, et al., Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors. Cell. 2014 Jul 3;158(1):198-212
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
05/21/2024
MGI 6.23
The Jackson Laboratory