ARPC3 — patent landscape

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

Compound	Confidence	Supporting neighbours
SCHEMBL4699731	1.00	2/20
SCHEMBL16111548	1.00	2/20
SCHEMBL29358745	1.00	2/20
SCHEMBL29380618	1.00	2/20
SCHEMBL29931136	1.00	2/20
SCHEMBL4697866	0.89	2/20
SCHEMBL24532075	0.89	2/20
SCHEMBL4697696	0.86	2/20
SCHEMBL23092285	0.86	2/20
SCHEMBL29688472	0.86	2/20
SCHEMBL22024695	0.86	2/20
SCHEMBL16136600	0.84	2/20
SCHEMBL24532058	0.83	2/20
SCHEMBL4699947	0.83	2/20
SCHEMBL22025026	0.82	2/20
SCHEMBL22119546	0.82	2/20
SCHEMBL24532062	0.82	2/20
SCHEMBL18804561	0.81	2/20
SCHEMBL22024561	0.81	2/20
SCHEMBL22025030	0.81	2/20

Clinical trials — most relevant to ARPC3 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome	PHASE2	RECRUITING
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Clinical and Biochemical Features for the Identification of Dominant Calpainopathies	nan	UNKNOWN
Family Blood Pressure Program - GenNet Network	nan	COMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease	nan	COMPLETED
Autophagy in Systemic Lupus Erythematosus	nan	UNKNOWN
Family Blood Pressure Program - HyperGEN	nan	COMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease	nan	COMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events	nan	COMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Family Blood Pressure Program - GENOA	nan	COMPLETED
Family Blood Pressure Program - SAPPHIRe Network	nan	COMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Evaluation of Limb-Girdle Muscular Dystrophy	nan	COMPLETED
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits	nan	COMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Molecular Genetics of Retinal Degenerations	nan	COMPLETED
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS	nan	RECRUITING
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Mayo AVC Registry and Biobank	nan	RECRUITING
Integrins and Protocadherins in Glutamatergic Circuits: Identification of Common Signaling Pathways and Molecular Targets in Anxiety and Major Depressive Disorders (GAPsy)	nan	UNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism	nan	COMPLETED
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES)	nan	COMPLETED
The Genetics of Cardiomyopathy and Heart Failure	nan	WITHDRAWN
PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read Sequencing	nan	RECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH)	nan	RECRUITING
Pediatric Cardiomyopathy Mutation Analysis	nan	RECRUITING

Related proteins — ESM-2 sequence neighbours (a ARPC3 binder may also engage these)

Protein	Name	Similarity
Q3T035	—	1.000	Q3T035 →
Q9JM76	—	1.000	Q9JM76 →
A1DPK7	—	1.000	A1DPK7 →
Q7T0U5	—	1.000	Q7T0U5 →
Q5AAJ8	—	0.995	Q5AAJ8 →
P09877	—	0.995	P09877 →
Q784P6	—	0.993	Q784P6 →
Q83HQ6	—	0.992	Q83HQ6 →
Q1WTX9	—	0.992	Q1WTX9 →
P20402	—	0.991	P20402 →
Q32RZ2	—	0.991	Q32RZ2 →
P38475	—	0.991	P38475 →
Q83GH5	—	0.991	Q83GH5 →
B4SCX8	—	0.991	B4SCX8 →
P0CT27	—	0.990	P0CT27 →
B4S4Y9	—	0.990	B4S4Y9 →
P86225	—	0.990	P86225 →
Q86UN6	—	0.990	Q86UN6 →
P23554	—	0.990	P23554 →
B3SRX0	—	0.990	B3SRX0 →
P18611	—	0.989	P18611 →
Q96FN9	—	0.989	Q96FN9 →
Q9W850	—	0.989	Q9W850 →
Q65231	—	0.989	Q65231 →
O48397	—	0.989	O48397 →
Q03245	—	0.989	Q03245 →
C7ZPG2	—	0.989	C7ZPG2 →
Q2VED6	—	0.989	Q2VED6 →
P05673	—	0.989	P05673 →
Q1ECJ7	—	0.989	Q1ECJ7 →