Scml2^{rs255759965-C}
Spontaneous Allele Detail

Summary

• Symbol: Scml2^{rs255759965-C}
• Name: Scm polycomb group protein like 2; rs255759965 SNP allele with the C variant
• MGI ID: MGI:6455218
• Gene: Scml2 Location: ChrX:159865521-160041209 bp, + strand Genetic Position: ChrX, 73.95 cM
• Alliance: Scml2^{rs255759965-C} page

Mutation origin

• Strain of Origin: various

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This spontaneous T-to-C mutation (ChrX:g.161192220T>C) changes leucine codon 145 to a proline codon (p.L145P). It is found in the BALB/cJ, BALB/cByJ, CAST/EiJ, LEWES/EiJ, MOLF/EiJ, NOD/ShiLtJ, PWK/PhJ, SEA/GnJ, SPRET/EiJ, WSB/EiJ, and ZALENDE/EiJ strains. (J:294207)

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 Scml2 Mutation: 11 strains or lines available

References

• Original: J:294207 Gan P, et al., Allelic variants between mouse substrains BALB/cJ and BALB/cByJ influence mononuclear cardiomyocyte composition and cardiomyocyte nuclear ploidy. Sci Rep. 2020 May 5;10(1):7605
• All: 1 reference(s)