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Slc2a10S150F
Chemically induced Allele Detail
Nomenclature
Symbol: Slc2a10S150F
Name: solute carrier family 2 (facilitated glucose transporter), member 10; Ser150Phe
MGI ID: MGI:3814339
Gene: Slc2a10  Location: Chr2:165503787-165519917 bp, + strand  Genetic Position: Chr2, 85.66 cM
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a single point mutation causing a C>T transition at position 449 that results in an amino acid substitution of phenylalanine for serine at position 150 (S150F). (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: 2 anatomical structures
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:  12 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:  2 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
05/15/2018
MGI 6.12
The Jackson Laboratory