Ctag2^rs29050889-G
Spontaneous Allele Detail

Summary

• Symbol: Ctag2^rs29050889-G
• Name: cancer/testis antigen 2; rs29050889 SNP allele with the G variant
• MGI ID: MGI:6477620
• Gene: Ctag2 Location: ChrX:64091250-64092620 bp, + strand Genetic Position: ChrX, 34.64 cM, cytoband A5
• Alliance: Ctag2^rs29050889-G page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This chrX:g.65047953T-to-G mutation (GRCm38 coordinates), which changes codon 90 from valine to glycine (p.V90G), is the minor variant of SNP rs29050889 that is found in the PWD and PWK strains. (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 Ctag2 Mutation: 2 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)