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Adam10Pied
Spontaneous Allele Detail
Summary
Symbol: Adam10Pied
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: Adam10Pied page
Mutation
origin
Strain of Origin:  HRA/SkhKcl
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe 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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:  37 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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory