ARCN1

Coatomer subunit delta · P48444 · ARCN1 on Sugi Atlas →

0 patent compounds predicted against ARCN1, 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 ARCN1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Dominantly Inherited Alzheimer Network Trial: An Opportunity to Prevent Dementia. A Study of Potential Disease Modifying Treatments in Individuals With a Type of Early Onset Alzheimer's Disease Caused by a Genetic Mutation (DIAN-TU) PHASE2/PHASE3ACTIVE_NOT_RECRUITING
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Clinical and Biochemical Features for the Identification of Dominant Calpainopathies nanUNKNOWN
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders nanRECRUITING
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models nanCOMPLETED
Validation of a Clinical Algorithm for the Diagnosis of Recessive Ataxias nanCOMPLETED
Clinical Outcome Study for Dysferlinopathy nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Defining the Brain Phenotype of Children With Williams Syndrome nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
The Predictive Factors of Good Clinical Response to Cholinesterase Inhibitors in Alzheimer Disease and Mixed Dementia nanCOMPLETED
Clinical Characterization on PDE6A-related Retinitis Pigmentosa in Preparation to a Gene Therapy Trial nanCOMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases nanCOMPLETED
Presymptomatic Neuromuscular Junction Defects and Compensatory Mechanisms in ALS nanUNKNOWN
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study nanACTIVE_NOT_RECRUITING

Related proteins — ESM-2 sequence neighbours (a ARCN1 binder may also engage these)

ProteinNameSimilarity
Q66H80 1.000 Q66H80 →
Q5XJY5 1.000 Q5XJY5 →
Q5RA77 1.000 Q5RA77 →
P53619 1.000 P53619 →
Q5ZL57 1.000 Q5ZL57 →
P17427 0.962 P17427 →
P18484 0.961 P18484 →
AP2A2 AP-2 complex subunit alpha-2 0.961 landscape →
Q6P856 0.960 Q6P856 →
Q5ZMP6 0.959 Q5ZMP6 →
Q3ZC13 0.958 Q3ZC13 →
P84091 0.958 P84091 →
Q5NVF7 0.958 Q5NVF7 →
Q4R706 0.957 Q4R706 →
AP2M1 AP-2 complex subunit mu 0.957 landscape →
Q801Q8 0.956 Q801Q8 →
Q6NWK2 0.955 Q6NWK2 →
P84092 0.955 P84092 →
Q0VCK5 0.955 Q0VCK5 →
O70133 0.954 O70133 →
Q5R648 0.953 Q5R648 →
DHX9 ATP-dependent RNA helicase A 0.953 landscape →
Q7ZW98 0.952 Q7ZW98 →
Q3SZA0 0.952 Q3SZA0 →
O88544 0.952 O88544 →
O55029 0.951 O55029 →
Q5R874 0.951 Q5R874 →
Q5XI73 0.951 Q5XI73 →
A2VDL8 0.950 A2VDL8 →
Q6NRT5 0.950 Q6NRT5 →