Slc12a7^mpc264H
Chemically induced Allele Detail

Summary

• Symbol: Slc12a7^mpc264H
• Name: solute carrier family 12, member 7; muta-ped-c3pde 264, Harwell
• MGI ID: MGI:5792092
• Gene: Slc12a7 Location: Chr13:73881213-73964873 bp, + strand Genetic Position: Chr13, 40.15 cM, cytoband C1
• Alliance: Slc12a7^mpc264H page

Mutation origin

• Strain of Origin: C57BL/6J
• Project Collection: Harwell ENU Mutagenesis

Mutation description

• Allele Type: Chemically induced (ENU) (Not Specified)
• Mutation: Single point mutation
• Mutation details: ENU mutagenesis induced a C to T point mutation that result in the amino acid substitution of a termination codon for glutamine at position 599 (Q599*). (J:234901)
• Inheritance: Recessive

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 Slc12a7 Mutation: 67 strains or lines available

References

• Original: J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
• All: 1 reference(s)