Selected-GenAtlas references	SOURCE	GeneCards	NCBI Gene	Swiss-Prot	Orphanet	Ensembl
	HGNC	UniGene	Nucleotide	OMIM		UCSC

Home Page

FLASH GENE

Symbol

ATP7A

contributors: mct - updated : 01-10-2017

HGNC name	ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome)
HGNC id	869

FLASH GENE DNA RNA EXPRESSION PROTEIN DISORDER ANIMAL & CELL MODELS

ASSOCIATED DISORDERS

corresponding disease(s)

MNK , OHS , DSMAX

Other morbid association(s)

Type Gene Modification Chromosome rearrangement Protein expression Protein Function constitutional     --low   contributes to impaired SOD3 activity, resulting in O2(•-) overproduction and endothelial dysfunction in blood vessels of T1 diabetes mellitus constitutional germinal mutation       mutation can delay the onset of prion disease

Susceptibility

Variant & Polymorphism

Candidate gene
Marker
Therapy target
	System Type Disorder Pubmed diabete metabolic syndrom   restoring copper transporter function is an essential therapeutic approach for oxidant stress-dependent vascular and metabolic diseases

ANIMAL & CELL MODELS