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Nfatc1tm1.1Fbs
Targeted Allele Detail
Summary
Symbol: Nfatc1tm1.1Fbs
Name: nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 1; targeted mutation 1.1, Friederike Berberich-Siebelt
MGI ID: MGI:7639766
Synonyms: Nfatc1deltaSUMO
Gene: Nfatc1  Location: Chr18:80649420-80756286 bp, - strand  Genetic Position: Chr18, 53.66 cM, cytoband E4
Alliance: Nfatc1tm1.1Fbs page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:305649
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  (BALB/c x C57BL/6)F1
Mutation
description
Allele Type:    Targeted (Not Applicable)
Mutation:    Nucleotide substitutions
 
Mutation detailsLysine codons 689 (AAG) and 896 (AAG) in exon 9 were changed to arginine (CGG) (ENSMUSP00000077196:p.K689R, ENSMUSP00000126884:p.K896R). A loxP site was inserted into intron 8 and a loxP site flanked neomycin resistance gene cassette was inserted into intron 9. The neo cassette was removed through subsequent Cre-mediated recombination. The mutations prevent sumoylation of the two affected residues in the encoded peptide. Cre-mediated deletion of the floxed exon 9 would specifically prevent the translation of a full-length betaC isoform. (J:305649)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Nfatc1 Mutation:  49 strains or lines available
References
Original:  J:305649 Xiao Y, et al., Lack of NFATc1 SUMOylation prevents autoimmunity and alloreactivity. J Exp Med. 2021 Jan 4;218(1)
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
10/29/2024
MGI 6.24
The Jackson Laboratory