ARPC2

Actin-related protein 2/3 complex subunit 2 · O15144 · ARPC2 on Sugi Atlas →

0 patent compounds predicted against ARPC2, 0 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to ARPC2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
Targeted Therapy With Glycogen Synthase Kinase-3 Inhibition for Arrhythmogenic Cardiomyopathy PHASE2RECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Family Blood Pressure Program - GENOA nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Mayo AVC Registry and Biobank nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
HYPOCHOL : A Genetically-based Strategy to Identify New Targets in Cholesterol Metabolism nanACTIVE_NOT_RECRUITING
PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read Sequencing nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Molecular Genetics of Retinal Degenerations nanCOMPLETED
Non-interventional Study of Seroprevalence of Pre-existing Antibodies Against Adenovirus-associated Virus Vector (AAV9) and the Progression of Disease in Patients With Plakophilin 2 (PKP2)-Associated Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) nanRECRUITING
Genes Modulating the Severity of Aortic Aneurysms (MSF1-TGFBR2) nanUNKNOWN
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
The Genetics of Cardiomyopathy and Heart Failure nanWITHDRAWN

Related proteins — ESM-2 sequence neighbours (a ARPC2 binder may also engage these)

ProteinNameSimilarity
P85970 1.000 P85970 →
Q5R5Z5 1.000 Q5R5Z5 →
Q0IH88 1.000 Q0IH88 →
Q3MHR7 1.000 Q3MHR7 →
Q9CVB6 1.000 Q9CVB6 →
Q6IRB1 0.999 Q6IRB1 →
O96623 0.997 O96623 →
Q03242 0.995 Q03242 →
P0DJU0 0.994 P0DJU0 →
P0DJV7 0.994 P0DJV7 →
P0CK89 0.994 P0CK89 →
A2T3P0 0.994 A2T3P0 →
P0DJV8 0.994 P0DJV8 →
A2RHI6 0.994 A2RHI6 →
P0DJR3 0.994 P0DJR3 →
Q09110 0.993 Q09110 →
P0DJU8 0.993 P0DJU8 →
P0CK85 0.993 P0CK85 →
Q8WTM6 0.993 Q8WTM6 →
Q5GT42 0.993 Q5GT42 →
Q8B6J9 0.993 Q8B6J9 →
P0DJR6 0.993 P0DJR6 →
P0CK65 0.993 P0CK65 →
P0DJV6 0.993 P0DJV6 →
P0DJS7 0.993 P0DJS7 →
P0CAB6 0.993 P0CAB6 →
P0C570 0.993 P0C570 →
P0DJU9 0.993 P0DJU9 →
Q8KEP5 0.993 Q8KEP5 →
B2GBW6 0.993 B2GBW6 →