Lhfpl2^vgim
Spontaneous Allele Detail

Summary

• Symbol: Lhfpl2^vgim
• Name: lipoma HMGIC fusion partner-like 2; vaginal imperforation
• MGI ID: MGI:4880679
• Gene: Lhfpl2 Location: Chr13:94194304-94331917 bp, + strand Genetic Position: Chr13, 49.03 cM
• Alliance: Lhfpl2^vgim page

Mutation origin

• Strain of Origin: B6.129S4-Ttpa^tm1Far/J

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: This spontaneous mutation has a G-to-A transition at chromosome 13 position 94,174,528 (GRCm38) which causes a glycine to glutamic acid substitution at amino acid 102 (p.G102E). (J:176116, J:219039, J:222308)
• Inheritance: Recessive

Expression

In Mice Carrying this Mutation:	2 assay results
In Structures Affected by this Mutation:	13 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Lhfpl2 Mutation: 16 strains or lines available

References

• Original: J:167822 Karst SY, et al., Vaginal imperforation; a new mutation on Chromosome 13 causing a reproductive phenotype. MGI Direct Data Submission. 2011
• All: 5 reference(s)