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Junctophilin 1
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle
Jejunum
Tongue main corpus
Tongue superior part with papillae
Caudate
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Disease Atlas
Most Correlated Diseases
Charcot-Marie-Tooth disease
Anomaly of chromosome pair 1
Anomaly of chromosome pair 17
Anomaly of chromosome pair 11
Bronchitis
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Pharmaco Atlas
Most Correlated Compounds
Taxol
Thrombopoietin
flt3 ligand protein
4-amino-6-hydrazino-7-beta-D-ribofuranosyl-7H-pyrrolo(2,3-d)-pyrimidine-5-carboxamide
17-hydroxyandrostane-3-glucuronide
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Knockdown Atlas
Most Correlated Gene Perturbations
CHMP2B
SATB2
SMARCC2
PTH1R
CLDN1
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial involvement.
Dissociation of SH3 and cysteine-rich domain 3 and junctophilin 1 from dihydropyridine receptor in d…
Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease.
Activation of p53/miR-34a Tumor Suppressor Axis by Chinese Herbal Formula JP-1 in A549 Lung Adenocar…
Expression of Junctophilin 1 during cardiogenesis of mouse embryonic stem cells and rat embryos].
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for Junctophilin 1
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