Adam10^Pied
Spontaneous Allele Detail

Summary

• Symbol: Adam10^Pied
• Name: a disintegrin and metallopeptidase domain 10; Pied
• MGI ID: MGI:6163474
• Gene: Adam10 Location: Chr9:70586279-70687511 bp, + strand Genetic Position: Chr9, 39.53 cM
• Alliance: Adam10^Pied page

Mutation origin

• Strain of Origin: HRA/SkhKcl

Mutation description

• Allele Type: Spontaneous (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: The spontaneous mutation consists of a deletion of 1914 base pairs, including all of exon 11, plus an insertion of 50 base pairs with homology to mouse L1 Line elements. (J:262499)
• Inheritance: Dominant

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 Adam10 Mutation: 38 strains or lines available

References

• Original: J:262499 Tharmarajah G, et al., Adam10 haploinsufficiency causes freckle-like macules in Hairless mice. Pigment Cell Melanoma Res. 2012 Sep;25(5):555-65
• All: 1 reference(s)