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Nfixtm1.1Rmg
Targeted Allele Detail
Summary
Symbol: Nfixtm1.1Rmg
Name: nuclear factor I/X; targeted mutation 1.1, Richard M Gronostajski
MGI ID: MGI:3802571
Gene: Nfix  Location: Chr8:85431341-85527086 bp, - strand  Genetic Position: Chr8, 41.02 cM, cytoband C1-C2
Alliance: Nfixtm1.1Rmg page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:137651
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsGerm line, cre-mediated recombination was used to remove the neo cassette and exon 2. The absence of transcript was confirmed by RT-PCR on liver extracts. (J:137651)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 4 assay results
1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 15 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 Nfix Mutation:  61 strains or lines available
References
Original:  J:137651 Campbell CE, et al., The transcription factor Nfix is essential for normal brain development. BMC Dev Biol. 2008;8:52
All:  17 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