QuickView for CACNA1D;jsessionid=0E89C21EA92C8F68272F1F0544F30669;jsessionid=BE758F029EA5C8048AA58170B3547718;jsessionid=884B22E5D2CA11FABB1AE19770102C53 (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

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.
CACNA1D overexpression and voltage-gated calcium channels in prostate cancer during androgen depriva…
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with …

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Clinical Trials

Most Relevant Clinical Trials

There were no clinical trials for CACNA1D;jsessionid=0E89C21EA92C8F68272F1F0544F30669;jsessionid=BE758F029EA5C8048AA58170B3547718;jsessionid=884B22E5D2CA11FABB1AE19770102C53

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