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Atp7aMo-17H
Chemically induced Allele Detail
Summary
Symbol: Atp7aMo-17H
Name: ATPase, copper transporting, alpha polypeptide; mottled 17 Harwell
MGI ID: MGI:2387458
Gene: Atp7a  Location: ChrX:105070882-105168532 bp, + strand  Genetic Position: ChrX, 47.36 cM
Alliance: Atp7aMo-17H page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Chemically induced (other)
Mutation:    Undefined
    This mutation was recovered from a chemical mutagenesis experiment at Harwell.
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
References
Original:  J:69983 Cunliffe P, et al., Intragenic deletions at atp7a in mouse models for menkes disease. Genomics. 2001 Jun 1;74(2):155-62
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
10/29/2024
MGI 6.24
The Jackson Laboratory