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Slc25a3tm1.1Jmol
Targeted Allele Detail
Summary
Symbol: Slc25a3tm1.1Jmol
Name: solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 3; targeted mutation 1.1, Jeffery Molkentin
MGI ID: MGI:6198542
Synonyms: Slc25a3fl
Gene: Slc25a3  Location: Chr10:90952436-90959902 bp, - strand  Genetic Position: Chr10, 45.6 cM
Alliance: Slc25a3tm1.1Jmol page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:229795
Parent Cell Line:  KG-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Conditional ready)
Mutation:    Insertion
 
Mutation detailsThe targeting construct contains loxP sites flanking exons 1 and 2. An FRT-flanked neomycin cassette is present in the construct, however, Flp-mediated recombination removed the cassette. (J:229795)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
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 Slc25a3 Mutation:  24 strains or lines available
References
Original:  J:229795 Kwong JQ, et al., Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathy. Cell Death Differ. 2014 Aug;21(8):1209-17
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
04/16/2024
MGI 6.23
The Jackson Laboratory