Slitrk2^m1
Spontaneous Allele Detail

Summary

• Symbol: Slitrk2^m1
• Name: SLIT and NTRK-like family, member 2; mutation 1
• MGI ID: MGI:6477643
• Gene: Slitrk2 Location: ChrX:65692924-65704999 bp, + strand Genetic Position: ChrX, 34.81 cM, cytoband A5
• Alliance: Slitrk2^m1 page

Mutation origin

• Strain of Origin: Not Applicable

Mutation description

• Allele Type: Spontaneous (Not Applicable)
• Mutation: Nucleotide substitutions
• Mutation details: This allele represents two point mutations that are found in the PWD and PWK strains: chrX:g.66655874A>G (the minor variants of SNP rs29051074; changes codon 657 from asparagine to serine (p.N657S)) and 66656111A>G (changes codon 736 from tyrosine to cysteine (p.Y736C) (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 Slitrk2 Mutation: 6 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)