4930447F04Rik^rs49812516-C
Spontaneous Allele Detail

Summary

• Symbol: 4930447F04Rik^rs49812516-C
• Name: RIKEN cDNA 4930447F04 gene; rs49812516 SNP allele with the C variant
• MGI ID: MGI:6477626
• Gene: 4930447F04Rik Location: ChrX:65346967-65347830 bp, - strand Genetic Position: ChrX, 34.69 cM, cytoband A5
• Alliance: 4930447F04Rik^rs49812516-C page

Mutation origin

• Strain of Origin: Not Applicable

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This chrX:g.66303564A>C mutation (GRCm38 coordinates), which changes codon 126 from phenylalanine to valine (p.F126V), is the minor variant of SNP rs49812516 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 4930447F04Rik 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)