Nhs^rs29303490-T
Spontaneous Allele Detail

Summary

• Symbol: Nhs^rs29303490-T
• Name: NHS actin remodeling regulator; rs29303490 SNP allele with the T variant
• MGI ID: MGI:6455219
• Gene: Nhs Location: ChrX:160616286-160942437 bp, - strand Genetic Position: ChrX, 74.17 cM
• Alliance: Nhs^rs29303490-T page

Mutation origin

• Strain of Origin: various

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This spontaneous G-to-A mutation (on reverse gene strand; ChrX:g.161842605C>T on forward strand) changes valine codon 583 to an isoleucine codon (p.V583I). It is found in the BALB/cJ, BALB/cByJ, CAST/EiJ, LEWES/EiJ, MOLF/EiJ, PWK/PhJ, SEA/GnJ, SPRET/EiJ, and WSB/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 Nhs Mutation: 20 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)