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Slc3a1pbl
Chemically induced Allele Detail
Nomenclature
Symbol: Slc3a1pbl
Name: solute carrier family 3, member 1; pebbles
MGI ID: MGI:2677291
Gene: Slc3a1  Location: Chr17:85028347-85064241 bp, + strand  Genetic Position: Chr17, 55.17 cM
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes 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
Carrying any Slc3a1 Mutation:  1 strain or line available
Notes
Possible involvement in Hartnup disorder (OMIM 234500), a syndrome of renal failure with thrombocytopenia and hemolytic anemia, has also been suggested (J:4747).

References
Original:  J:85461 Peters T, et al., A mouse model for cystinuria type I. Hum Mol Genet. 2003 Sep 1;12(17):2109-20
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/11/2014
MGI 5.20
The Jackson Laboratory