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Syngap1em1Rlh
Endonuclease-mediated Allele Detail
Summary
Symbol: Syngap1em1Rlh
Name: synaptic Ras GTPase activating protein 1 homolog (rat); endonuclease-mediated mutation 1, Richard Huganir
MGI ID: MGI:7514997
Synonyms: Syngap1L813Rfsx22
Gene: Syngap1  Location: Chr17:27160227-27191408 bp, + strand  Genetic Position: Chr17, 13.6 cM
Alliance: Syngap1em1Rlh page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/cas9 endonuclease-mediated genome editing is used to delete a single base at c.2438 (T) creating a frameshift mutation, L813Rfsx22, in exon 15. The deletion was confirmed by sequencing and Southern blot. (J:341855)
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 Syngap1 Mutation:  49 strains or lines available
References
Original:  J:341855 Araki Y, et al., Mouse models of SYNGAP1-related intellectual disability. Proc Natl Acad Sci U S A. 2023 Sep 12;120(37):e2308891120
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