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Scn1aem6(IMPC)Tcp
Endonuclease-mediated Allele Detail
Summary
Symbol: Scn1aem6(IMPC)Tcp
Name: sodium channel, voltage-gated, type I, alpha; endonuclease-mediated mutation 6, The Centre for Phenogenomics
MGI ID: MGI:5755084
Gene: Scn1a  Location: Chr2:66101125-66271181 bp, - strand  Genetic Position: Chr2, 39.13 cM
Alliance: Scn1aem6(IMPC)Tcp page
IMPC: Scn1a gene page
Mutation
origin
Strain of Origin:  C57BL/6NCrl
Project Collection: IMPC
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThis allele, from project TCPR0246, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and one guide RNA with spacer sequence AGTCGTTCATGTGCCAACGT. This resulted in a 1 bp insertion at Chr2:66319540 in OTTMUSE00000158516. This mutation is predicted to cause a frameshift with amino acid changes after residue 932 and early truncation 63 amino acids later (p.W932Lfs*65). (GRCm38). (J:165963)
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 Scn1a Mutation:  114 strains or lines available
References
Original:  J:165963 Centre for Modeling Human Disease, Alleles produced for the NorCOMM project by the Centre for Modeling Human Disease (Cmhd), Institute of Biomaterials & Biomedical Engineering, University of Toronto. MGI Direct Data Submission. 2010;
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
05/07/2024
MGI 6.23
The Jackson Laboratory