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Atp7aMo-12DFiOD
Radiation induced Allele Detail
Summary
Symbol: Atp7aMo-12DFiOD
Name: ATPase, copper transporting, alpha polypeptide; mottled Oak Ridge 12DFiOD
MGI ID: MGI:2387948
Synonyms: Atp7amo12DFiOD, Xmo21R
Gene: Atp7a  Location: ChrX:105070882-105168532 bp, + strand  Genetic Position: ChrX, 47.36 cM
Alliance: Atp7aMo-12DFiOD page
Mutation
origin
Strain of Origin:  T STOCK x (101 x C3H)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Undefined
    An induced mutation that was created at The Oak Ridge National Laboratory.
Inheritance:    Semidominant
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 Atp7a Mutation:  69 strains or lines available
Notes
This mutation is lethal to hemizygous male embryos (J:38977).
References
Original:  J:38977 Cecchi C, et al., The mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene. (Correction: vol. 6(5):829). Hum Mol Genet. 1997 Mar;6(3):425-33
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
10/22/2024
MGI 6.24
The Jackson Laboratory