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Tg(PGK1-FTL*)#Sle
Transgene Detail
Summary
Symbol: Tg(PGK1-FTL*)#Sle
Name: transgene insertion, Sonia Levi
MGI ID: MGI:5700531
Synonyms: FTL-498InsTC
Transgene: Tg(PGK1-FTL*)#Sle  Location: unknown  
Alliance: Tg(PGK1-FTL*)#Sle page
Transgene
origin
Strain of Origin:  FVB/N
Transgene
description
Transgene Type:    Transgenic (Humanized sequence, Inserted expressed sequence)
Mutation:    Insertion
 
Tg(PGK1-FTL*)#Sle expresses 1 gene
 
Mutation detailsThe constitutive and ubiquitous human PGK1 promoter drives the expression of the human cDNA bearing the 498-499InsTC mutation causing the substitution of the last 9 amino acids and an elongation of extra 16 amino acids at the C-terminus of L-ferritin peptide. This modification reduces the ability of the protein to store iron. ELISA and Immunoblotting confirm high expression of the transgene in the liver and brain. Although three lines were obtained, only one was used for further analysis. However, line numbers were not identified and the pound (#) symbol is used because the line number is not specified. (J:227451)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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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
References
Original:  J:227451 Maccarinelli F, et al., A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits. Neurobiol Dis. 2015 Sep;81:119-33
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
04/16/2024
MGI 6.23
The Jackson Laboratory