ARPC4

Actin-related protein 2/3 complex subunit 4 · P59998 · ARPC4 on Sugi Atlas →

0 patent compounds predicted against ARPC4, 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 ARPC4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Family Blood Pressure Program - GENOA nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES) nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
The Role of TBC1D4 in Exercise- and Insulin-induced Glucose Metabolism in Human Skeletal Muscle nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
GARM II: A Study on the Genetics of Age-related Maculopathy nanACTIVE_NOT_RECRUITING
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a ARPC4 binder may also engage these)

ProteinNameSimilarity
Q148J6 1.000 Q148J6 →
P59999 1.000 P59999 →
Q641G7 1.000 Q641G7 →
Q9HD40 0.948 Q9HD40 →
Q5RAK7 0.946 Q5RAK7 →
Q803A7 0.944 Q803A7 →
Q28EN2 0.942 Q28EN2 →
Q6P6M7 0.941 Q6P6M7 →
Q8BWQ6 0.941 Q8BWQ6 →
Q3B8M3 0.940 Q3B8M3 →
D2SW95 0.937 D2SW95 →
Q7Z3J2 0.937 Q7Z3J2 →
Q6DRI1 0.937 Q6DRI1 →
Q5R6E0 0.937 Q5R6E0 →
B5DGH9 0.937 B5DGH9 →
Q5ZIA5 0.936 Q5ZIA5 →
Q6P7L9 0.936 Q6P7L9 →
Q5F3X4 0.936 Q5F3X4 →
Q5ZLA5 0.936 Q5ZLA5 →
COPB1 Coatomer subunit beta 0.935 landscape →
A0JN39 0.935 A0JN39 →
Q9JIF7 0.935 Q9JIF7 →
A9JRA0 0.935 A9JRA0 →
Q5R8N4 0.934 Q5R8N4 →
P23514 0.934 P23514 →
Q5R922 0.934 Q5R922 →
A4FUD3 0.934 A4FUD3 →
Q05AY2 0.934 Q05AY2 →
Q0P5J8 0.933 Q0P5J8 →
Q40281 0.933 Q40281 →