CCT6A

T-complex protein 1 subunit zeta · P40227 · CCT6A on Sugi Atlas →

0 patent compounds predicted against CCT6A, 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 CCT6A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Danazol for Genetic Bone Marrow and Lung Disorders PHASE1/PHASE2COMPLETED
A Phase Ib/II Clinical Study Evaluating the Safety and Efficacy of Tislelizumab in Combination With Golidocitinib and Selinexor for the Treatment of R/R NKTCL PHASE1/PHASE2RECRUITING
Effect of Deferoxamine on Wound Healing Rate in Patients With Diabetes Foot Ulcers PHASE2NOT_YET_RECRUITING
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Assessment Of Long Noncoding RNA CCAT1 In Colorectal Cancer Patients nanUNKNOWN
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
PCM1-JAK2 in Therapy Related Neoplasms nanUNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Identification of Genetic Causes of Calcific Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a CCT6A binder may also engage these)

ProteinNameSimilarity
O77622 0.993 O77622 →
P80317 0.993 P80317 →
Q4R5G2 0.993 Q4R5G2 →
Q9XT06 0.993 Q9XT06 →
Q32L40 0.993 Q32L40 →
Q5ZJ54 0.993 Q5ZJ54 →
Q5RCD2 0.992 Q5RCD2 →
Q9W790 0.992 Q9W790 →
P12613 0.992 P12613 →
P11983 0.992 P11983 →
O15891 0.991 O15891 →
P80313 0.991 P80313 →
P87153 0.991 P87153 →
Q92526 0.991 Q92526 →
TCP1 T-complex protein 1 subunit alpha 0.991 landscape →
Q5R5C8 0.990 Q5R5C8 →
Q3T084 0.990 Q3T084 →
Q8L7N0 0.990 Q8L7N0 →
P18279 0.990 P18279 →
Q3MHL7 0.990 Q3MHL7 →
Q2NKZ1 0.990 Q2NKZ1 →
Q5ZJK8 0.990 Q5ZJK8 →
CCT7 T-complex protein 1 subunit eta 0.990 landscape →
P28480 0.989 P28480 →
O94501 0.989 O94501 →
Q9SF16 0.989 Q9SF16 →
Q61390 0.989 Q61390 →
Q94757 0.988 Q94757 →
P46550 0.988 P46550 →
Q76NU3 0.988 Q76NU3 →