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Atp7aMo-12H
Spontaneous Allele Detail
Summary
Symbol: Atp7aMo-12H
Name: ATPase, copper transporting, alpha polypeptide; mottled 12 Harwell
MGI ID: MGI:1856324
Gene: Atp7a  Location: ChrX:105070882-105168532 bp, + strand  Genetic Position: ChrX, 47.36 cM
Alliance: Atp7aMo-12H page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsThis mutation arose in mutagenesis studies at Harwell. Linkage and inheritance tests suggested that this is mutation is allelic to Mottled.
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Atp7a Mutation:  69 strains or lines available
Notes
The mutation was found after induced in (C3H/HeH x 101/H)F1 males with hydroxyurea and X-rays, which were then mated to PT tester Stock females. Genetic analysis demonstrated that the mutation was derived from the PT tester stock, and is thought to be spontaneous.
References
Original:  J:16303 Rasberry C, et al., Three new mottled mutations - Mo10H, Mo11H, and Mo12H. Mouse Genome. 1993;91(4):851-53
All:  3 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
10/22/2024
MGI 6.24
The Jackson Laboratory