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C9orf72tm1.1Eggn
Targeted Allele Detail
Summary
Symbol: C9orf72tm1.1Eggn
Name: C9orf72, member of C9orf72-SMCR8 complex; targeted mutation 1.1, Kevin Eggan
MGI ID: MGI:5883590
Synonyms: -/- neo deleted, -/- Neo deleted
Gene: C9orf72  Location: Chr4:35191285-35226153 bp, - strand  Genetic Position: Chr4, 17.13 cM
Alliance: C9orf72tm1.1Eggn page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:240357
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6N
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsTarget vector was designed in the National Institutes of Health Knockout Mouse (KOMP) project. A lacZ gene and frt-flanked neomycin selection cassette replaced exons 2 through 6. Flp-mediated recommbination removed the neomycin selection cassette in mice. (J:240357)
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 C9orf72 Mutation:  36 strains or lines available
References
Original:  J:240357 Burberry A, et al., Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease. Sci Transl Med. 2016 Jul 13;8(347):347ra93
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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Funding Information
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory