Vgll1^rs31755951-A
Spontaneous Allele Detail

Summary

• Symbol: Vgll1^rs31755951-A
• Name: vestigial like family member 1; rs31755951 SNP allele with the A variant
• MGI ID: MGI:6455203
• Gene: Vgll1 Location: ChrX:56133466-56151900 bp, + strand Genetic Position: ChrX, 30.89 cM
• Alliance: Vgll1^rs31755951-A page

Mutation origin

• Strain of Origin: various

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This spontaneous G-to-A mutation (ChrX:g.57092486G>A) changes glycine codon 72 to an arginine codon (p.G72R) and changes splice donor site G-GT to A-GT. It is only found in the A/J, BALB/cJ, BALB/cByJ, C3HeH, C3HeJ, and SEA/GnJ 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 Vgll1 Mutation: 8 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)