Gm14692^m1
Spontaneous Allele Detail

Summary

• Symbol: Gm14692^m1
• Name: predicted gene 14692; mutation 1
• MGI ID: MGI:6477988
• Gene: Gm14692 Location: ChrX:66739304-66749956 bp, + strand Genetic Position: ChrX, 34.81 cM
• Alliance: Gm14692^m1 page

Mutation origin

• Strain of Origin: PWK

Mutation description

• Allele Type: Spontaneous
• Mutation: Nucleotide substitutions
• Mutation details: This allele represents three point mutations that are found in the PWK strain: chrX:g.67695723AA>CC (changes codon 9 from lysine to threonine (p.K9T)) and 67695771A>G (changes codon 25 from aspartic acid to glycine (p.D25G)) (GRCm38 coordinates). (J:292550)

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 Gm14692 Mutation: 0 strains or lines available

References

• Original: J:292550 Morimoto K, et al., Reverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis. Sci Rep. 2020 Jun 3;10(1):9060
• All: 1 reference(s)