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Slc2a10G128E
Chemically induced Allele Detail
Summary
Symbol: Slc2a10G128E
Name: solute carrier family 2 (facilitated glucose transporter), member 10; Gly128Glu
MGI ID: MGI:3814338
Gene: Slc2a10  Location: Chr2:165345817-165361837 bp, + strand  Genetic Position: Chr2, 85.66 cM
Alliance: Slc2a10G128E page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU induced a point mutation of G>A at position 383 that results in the amino acid substitution of glutamic acid for glycine at position 128 (G128E). (J:140316)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 12 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 Slc2a10 Mutation:  27 strains or lines available
References
Original:  J:140316 Callewaert BL, et al., Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions. Genesis. 2008 Aug;46(8):385-9
All:  5 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
03/12/2024
MGI 6.23
The Jackson Laboratory