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Nlgn3tm1.1Htz
Targeted Allele Detail
Summary
Symbol: Nlgn3tm1.1Htz
Name: neuroligin 3; targeted mutation 1.1, Nathaniel Heintz
MGI ID: MGI:4867464
Gene: Nlgn3  Location: ChrX:100342785-100364956 bp, + strand  Genetic Position: ChrX, 43.95 cM
Alliance: Nlgn3tm1.1Htz page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:167116
Parent Cell Line:  C2J (ES Cell)
Strain of Origin:  B6(Cg)-Tyrc-2J/J
Mutation
description
Allele Type:    Targeted
Mutation:    Nucleotide substitutions
 
Mutation detailsThe nucleotide sequence CGT in exon 6 which encodes Arginine at amino acid position 451 was modified to TGC which encodes Cysteine. A floxed neomycin cassette was also inserted in intron 6. The selection cassette was subsequently excised by crossing to Tg(EIIa-cre)C5379Lmgd mice. (J:167116)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:  36 strains or lines available
References
Original:  J:167116 Chadman KK, et al., Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice. Autism Res. 2008 Jun;1(3):147-58
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
12/10/2024
MGI 6.24
The Jackson Laboratory