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CACNA1D;jsessionid=328F7090757D395804F6858236C26ADA;jsessionid=DE051EB7AEF6B3B3E0A53430D6C97575
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Cerebellum peduncles
Skeletal muscle psoas
Atrioventricular node
Cingulate cortex
Tongue
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Disease Atlas
Most Correlated Diseases
Disorder of adrenal gland
Neurological finding
Infection by Encephalitozoon cuniculi
General adaptation syndrome
Pyloric ulcer
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Pharmaco Atlas
Most Correlated Compounds
senkirkine
Pyrrolizidine Alkaloids
8-(3-Chlorostyryl)-1,3,7-trimethylxanthine
Carbon Black
Organophosphorus Compounds
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Knockdown Atlas
Most Correlated Gene Perturbations
TMPRSS2
RBPMS
MARCH6
AXL
HNRNPA0
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
CaV1.3 channel clusters characterized by live-cell and isolated plasma membrane nanoscopy.
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mo…
CACNA1D-Related Channelopathies: From Hypertension to Autism.
The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndr…
Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for CACNA1D;jsessionid=328F7090757D395804F6858236C26ADA;jsessionid=DE051EB7AEF6B3B3E0A53430D6C97575
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