COPG2

Coatomer subunit gamma-2 · Q9UBF2 · COPG2 on Sugi Atlas →

0 patent compounds predicted against COPG2, 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 COPG2 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
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Non Motor Symptoms in Glucocerebrosidase-related Parkinson's Disease nanENROLLING_BY_INVITATION
Identification of New FTLD Genes nanUNKNOWN
Implementation of Molecular Diagnostic Pathways nanUNKNOWN
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Natural History of Limb Girdle Muscular Dystrophy Type 2A and Type 2E nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Anesthetic Methods and Gene Expression Profile nanCOMPLETED
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study nanACTIVE_NOT_RECRUITING
A Multicenter Phenotype-Genotype Analysis of LGMD Patients in China nanENROLLING_BY_INVITATION
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Genetic Studies of Chronic Active Epstein-Barr Disease nanRECRUITING
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Study of Schizophrenia nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a COPG2 binder may also engage these)

ProteinNameSimilarity
Q9QXK3 1.000 Q9QXK3 →
Q66JI9 1.000 Q66JI9 →
Q9I8E6 1.000 Q9I8E6 →
Q9PUE4 1.000 Q9PUE4 →
Q9QZE5 1.000 Q9QZE5 →
COPG1 Coatomer subunit gamma-1 1.000 landscape →
Q6DKD7 1.000 Q6DKD7 →
A2VE21 1.000 A2VE21 →
P53620 1.000 P53620 →
Q8I0G5 1.000 Q8I0G5 →
Q4AEF8 1.000 Q4AEF8 →
Q29AE5 1.000 Q29AE5 →
Q0WW26 0.998 Q0WW26 →
Q7PVF6 0.996 Q7PVF6 →
P22892 0.995 P22892 →
Q6Z382 0.995 Q6Z382 →
AP1G1 AP-1 complex subunit gamma-1 0.993 landscape →
Q8H852 0.993 Q8H852 →
Q22498 0.992 Q22498 →
Q9ZUI6 0.992 Q9ZUI6 →
Q29G21 0.992 Q29G21 →
Q84K16 0.991 Q84K16 →
P45437 0.991 P45437 →
Q5R5M2 0.988 Q5R5M2 →
Q54X82 0.988 Q54X82 →
AP3B1 AP-3 complex subunit beta-1 0.988 landscape →
PSMD2 26S proteasome non-ATPase regulatory subunit 2 0.988 landscape →
Q5R9I6 0.988 Q5R9I6 →
Q17D30 0.987 Q17D30 →
Q99128 0.987 Q99128 →