QuickView for ATP7A;jsessionid=D6F5FD099836092B91685533A3BAA91E;jsessionid=FB5E4726EF2093DA9204AE3BC3A2773B;jsessionid=5AFDB781692A5E4E95CB9F30C319DDEA (gene)

Summary
General Info

Body Atlas

Most Correlated Tissues

Neutrophil of bone marrow
Eosinophil of peripheral blood
Basophil of peripheral blood
Leukocyte (polymorphonuclear) of peripheral blood
Peritoneum

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Disease Atlas

Most Correlated Diseases

Menkes kinky-hair syndrome
Ehlers-Danlos syndrome
Congenital anomaly of integument
Skeletal dysplasia
Muscle atrophy

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Pharmaco Atlas

Most Correlated Compounds

Benperidol
naphthalene
Indinavir
MG 0103
antimycin

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Knockdown Atlas

Most Correlated Gene Perturbations

Mir139
Relb
TENM1
VDAC1
ANLN

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Curated Studies

Most Correlated Studies

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Literature

Most Relevant Literature

Deep intronic variant causes aberrant splicing of ATP7A in a family with a variable occipital horn s…
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtype…
ATP7A-dependent copper sequestration contributes to termination of β-CATENIN signaling during early …
Copper transporter gene ATP7A: A predictive biomarker for immunotherapy and targeted therapy in hepa…
Analysis of clinical characteristics and ATP7A gene variants in a Chinese pedigree affected with Men…

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Clinical Trials

Most Relevant Clinical Trials

There were no clinical trials for ATP7A;jsessionid=D6F5FD099836092B91685533A3BAA91E;jsessionid=FB5E4726EF2093DA9204AE3BC3A2773B;jsessionid=5AFDB781692A5E4E95CB9F30C319DDEA

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