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Slc11a2tm1Nca
Targeted Allele Detail
Summary
Symbol: Slc11a2tm1Nca
Name: solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2; targeted mutation 1, Nancy C Andrews
MGI ID: MGI:3577914
Synonyms: Slc11a2-
Gene: Slc11a2  Location: Chr15:100285779-100322090 bp, - strand  Genetic Position: Chr15, 56.29 cM
Alliance: Slc11a2tm1Nca page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:98088
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA cassette containing neomycin and cytidine deaminase flanked by loxP sites was replaced exons 6-8, which correspond to predicted transmembrane segments 3-5. (J:98088)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc11a2 Mutation:  38 strains or lines available
References
Original:  J:98088 Gunshin H, et al., Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver. J Clin Invest. 2005 May 2;115(5):1258-1266
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