COPG1

Coatomer subunit gamma-1 · Q9Y678 · COPG1 on Sugi Atlas →

0 patent compounds predicted against COPG1, 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 COPG1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
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
Ambroxol Therapy for Patients With Type 1 Gaucher Disease and Suboptimal Response to Enzyme Replacement Therapy PHASE2COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Implementation of Molecular Diagnostic Pathways nanUNKNOWN
A Multicenter Phenotype-Genotype Analysis of LGMD Patients in China nanENROLLING_BY_INVITATION
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Defining the Genetic Etiology of Alzheimer's Disease in the Faroe Islands nanUNKNOWN
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Inherited Reproductive Disorders nanRECRUITING
Clinical Characterization on PDE6A-related Retinitis Pigmentosa in Preparation to a Gene Therapy Trial nanCOMPLETED
Non Motor Symptoms in Glucocerebrosidase-related Parkinson's Disease nanENROLLING_BY_INVITATION
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Clinical Outcome Study for Dysferlinopathy nanUNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Mapping Disease Pathways for Biliary Atresia nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a COPG1 binder may also engage these)

ProteinNameSimilarity
P53620 1.000 P53620 →
Q0WW26 1.000 Q0WW26 →
Q9QZE5 1.000 Q9QZE5 →
Q9I8E6 1.000 Q9I8E6 →
Q9QXK3 1.000 Q9QXK3 →
Q9PUE4 1.000 Q9PUE4 →
Q66JI9 1.000 Q66JI9 →
COPG2 Coatomer subunit gamma-2 1.000 landscape →
Q6DKD7 1.000 Q6DKD7 →
Q4AEF8 0.999 Q4AEF8 →
Q22498 0.998 Q22498 →
Q8I0G5 0.997 Q8I0G5 →
A2VE21 0.997 A2VE21 →
Q29AE5 0.996 Q29AE5 →
Q5R5M2 0.995 Q5R5M2 →
O81742 0.994 O81742 →
Q7PVF6 0.993 Q7PVF6 →
Q9SUS3 0.993 Q9SUS3 →
Q54HL0 0.992 Q54HL0 →
Q6Z382 0.992 Q6Z382 →
Q9Z1T1 0.991 Q9Z1T1 →
P22892 0.990 P22892 →
P87140 0.990 P87140 →
Q9JME5 0.990 Q9JME5 →
AP1G1 AP-1 complex subunit gamma-1 0.989 landscape →
Q8LPL6 0.989 Q8LPL6 →
Q13367 0.989 Q13367 →
Q8H852 0.989 Q8H852 →
AP3D1 AP-3 complex subunit delta-1 0.989 landscape →
Q9SIV2 0.989 Q9SIV2 →