PB 13543
Description
Hair pigmentation variation. The sole phenotype noted in hemizygous male and homozygous female pewter mice is their pale, silvery gray coat color.
MPATH / Pathology
MPATH 56 - developmental or adult structural defect
Gene
ATPase, Cu++ transporting, alpha polypeptide
Atp7a
sex
Unknown
strain
CBA/J-Atp7aMo-pew/+
organism
Mouse
EMAP / Embryonic stage, tissue or post-natal age:
genotype status
Heterozygous
genetic manipulation
Spontaneous-mutant
MA / Anatomical Site
MA 159 - hair shaft
Designated Allele Name
Mo-pew
pewter
Experimental Manipulation
Further info
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Copyright
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Gene Ontology
GO ID: 0000287 - magnesium ion binding GO ID: 0004008 - copper-exporting ATPase activity GO ID: 0005507 - copper ion binding GO ID: 0005524 - ATP binding GO ID: 0005794 - Golgi apparatus GO ID: 0005889 - hydrogen/potassium-exchanging ATPase complex GO ID: 0006812 - cation transport GO ID: 0006825 - copper ion transport GO ID: 0008152 - metabolism GO ID: 0015662 - P-type ATPase activity GO ID: 0016020 - membrane GO ID: 0016021 - integral to membrane GO ID: 0016021 - integral to membrane GO ID: 0016787 - hydrolase activity GO ID: 0030001 - metal ion transport GO ID: 0046872 - metal ion binding