Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Slc2a10S150F
Name:	solute carrier family 2 (facilitated glucose transporter), member 10; Ser150Phe
MGI ID:	MGI:3814339
Gene:	Slc2a10  Location: Chr2:165345817-165361837 bp, + strand  Genetic Position: Chr2, 85.66 cM
Alliance:	Slc2a10S150F page

Strain of Origin:

C3HeB/FeJ

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: ENU 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)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

2 anatomical structure(s)

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

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)