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AMPD2;jsessionid=40729FB85CB550C49502E7CF4C8711F1
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Leukocyte (polymorphonuclear) of peripheral blood
Macrophage of peripheral blood
Neutrophil of bone marrow
Eosinophil of peripheral blood
Pituitary gland
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Disease Atlas
Most Correlated Diseases
Coliform mastitis
Congenital cerebellar hypoplasia
Amnestic disorder
Exercise
Hemoglobinopathy
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Pharmaco Atlas
Most Correlated Compounds
trilinolenin
ompP2 protein, Haemophilus influenzae
bacterial lysate
COOH-terminal signal transamidase
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
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Knockdown Atlas
Most Correlated Gene Perturbations
Mir9-3
daf-7
RPS6KL1
NRL
CDK8
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Delayed-Onset ADA1 (ADA) Deficiency Not Detected by TREC Screen.
A mutation in Ampd2 is associated with nephrotic syndrome and hypercholesterolemia in mice.
AMPD2 plays important roles in regulating hepatic glucose and lipid metabolism.
A Method for Production of Human Adenosine Deaminase 1 (ADA1) in Pichia pastoris Provides Needed Qua…
Distinct Roles of Adenosine Deaminase Isoenzymes ADA1 and ADA2: A Pan-Cancer Analysis.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for AMPD2;jsessionid=40729FB85CB550C49502E7CF4C8711F1
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