Pathbase: PB 13544


Pathbase Image PB 13544 submitted by Pathbase on 2003-08-12
Gene:ATPase, Cu++ transporting, alpha polypeptide
EMAP / Embryonic stage,
tissue or post-natal age:
Genotype Status:Heterozygous
MPATH / Pathology:MPATH 56 - developmental or adult structural defect
Genetic Manipulation:Spontaneous-mutant
MA / Anatomical Site:MA 159 - hair shaft
Designated Allele Name:Mo-pew
Experimental Manipulation:
Description:Hair pigmentation variation. The sole phenotype noted in hemizygous male and homozygous female pewter mice is their pale, silvery gray coat color.


Further Information
Gene Ontology Terms associated with the genes involved in this lesion may be searched on AMIGO by clicking on each GO ID number below:
Search AmiGO:GO ID: 0000287 - magnesium ion binding
Search AmiGO:GO ID: 0004008 - copper-exporting ATPase activity
Search AmiGO:GO ID: 0005507 - copper ion binding
Search AmiGO:GO ID: 0005524 - ATP binding
Search AmiGO:GO ID: 0005794 - Golgi apparatus
Search AmiGO:GO ID: 0005889 - hydrogen/potassium-exchanging ATPase complex
Search AmiGO:GO ID: 0006812 - cation transport
Search AmiGO:GO ID: 0006825 - copper ion transport
Search AmiGO:GO ID: 0008152 - metabolism
Search AmiGO:GO ID: 0015662 - P-type ATPase activity
Search AmiGO:GO ID: 0016020 - membrane
Search AmiGO:GO ID: 0016021 - integral to membrane
Search AmiGO:GO ID: 0016021 - integral to membrane
Search AmiGO:GO ID: 0016787 - hydrolase activity
Search AmiGO:GO ID: 0030001 - metal ion transport
Search AmiGO:GO ID: 0046872 - metal ion binding
Search PubMed:PubMed number: 8054976
Search MGI@Jax:Gene: Atp7a
Search MGI@Jax:Gene: ATPase, Cu++ transporting, alpha polypeptide
Images of the same study:Study number: 2152
NOTE: Not all terms are currently shared between Pathbase and the above databases, some searches may not produce returns, in which case users should use synonyms or more inclusive text terms to search manually!

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