Fmn1^ld-Lsk
Spontaneous Allele Detail

Summary

• Symbol: Fmn1^ld-Lsk
• Name: formin 1; limb deformity, Lawrence S Kirschner
• MGI ID: MGI:3718051
• Gene: Fmn1 Location: Chr2:113158081-113547112 bp, + strand Genetic Position: Chr2, 57.3 cM, cytoband C1-qter
• Alliance: Fmn1^ld-Lsk page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Spontaneous
• Mutation: Deletion
• Fmn1^ld-Lsk involves 1 genes/genome features (Fmn1) View all
• The complete locus is deleted, including its transcriptional global control region (GCR). (J:123068)

Expression

In Mice Carrying this Mutation:

216 assay results

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 Fmn1 Mutation: 75 strains or lines available

References

• Original: J:123068 Pavel E, et al., Analysis of a new allele of limb deformity (ld) reveals tissue- and age-specific transcriptional effects of the Ld Global Control Region. Int J Dev Biol. 2007;51(4):273-81
• All: 1 reference(s)