Slc2a10^S150F
Chemically induced Allele Detail

Summary

• Symbol: Slc2a10^S150F
• 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: Slc2a10^S150F page

Mutation origin

• Strain of Origin: C3HeB/FeJ

Mutation description

• 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)

Disease models

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 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: 2 reference(s)