Slc7a9^cys
Spontaneous Allele Detail

Summary

• Symbol: Slc7a9^cys
• Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 9; cystinuria
• MGI ID: MGI:7491962
• Gene: Slc7a9 Location: Chr7:35148221-35165461 bp, + strand Genetic Position: Chr7, 21.37 cM, cytoband B1
• Alliance: Slc7a9^cys page

Mutation origin

• Strain of Origin: FVB/NJcl

Mutation description

• Allele Type: Spontaneous (Null/knockout)
• Mutation: Intragenic deletion
• A spontaneous mutation deleted a large portion of the promoter region. (J:336716)
• Inheritance: Recessive

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Slc7a9 Mutation: 34 strains or lines available

References

• Original: J:336716 Sasaki H, et al., A mouse model of type B cystinuria due to spontaneous mutation in FVB/NJcl mice. Urolithiasis. 2022;50(6):679-684
• All: 1 reference(s)