Fnld
Radiation induced Allele Detail

Summary

• Symbol: Fnld
• Name: faint-lined
• MGI ID: MGI:1889331
• Gene: Fnld Location: ChrX:36059304-47772849 bp Genetic Position: ChrX, Syntenic
• Alliance: Fnld page

Mutation origin

• Strain of Origin: (C3H/HeH x 101/H)F1

Mutation description

• Allele Type: Radiation induced
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

2 anatomical structure(s)

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 Fnld Mutation: 0 strains or lines available

References

• Original: J:52809 Gormally E, et al., Faint lined (Fnl): a novel X-linked coat mutant in the mouse. Genet Res. 1998 Dec;72(3):211-6
• All: 1 reference(s)