CCT7

T-complex protein 1 subunit eta · Q99832 · CCT7 on Sugi Atlas →

0 patent compounds predicted against CCT7, 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 CCT7 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Addition of Everolimus to Standard of Care in Carcinoma Gallbladder PHASE2/PHASE3RECRUITING
Sirolimus Treatment in Patients With Autosomal Dominant Polycystic Kidney Disease: Renal Efficacy and Safety PHASE2COMPLETED
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Danazol for Genetic Bone Marrow and Lung Disorders PHASE1/PHASE2COMPLETED
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics nanUNKNOWN
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Genetic Diagnosis in Congenital Cataracts nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Telomere Disclosure and Impact on Psychological Distress and Health Behaviors nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Whole Exome Sequencing in Coronary Artery Ectasia nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Clinical and Genetic Studies of Families With Congenital or Hereditary Cataracts nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Correlation Between Myocardial Deformation and Coronary Artery Tortuosity in Patients With Hypertrophic Cardiomyopathy nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Assessment Of Long Noncoding RNA CCAT1 In Colorectal Cancer Patients nanUNKNOWN
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CCT7 binder may also engage these)

ProteinNameSimilarity
Q5R5C8 1.000 Q5R5C8 →
P80313 1.000 P80313 →
Q2NKZ1 1.000 Q2NKZ1 →
Q5ZJK8 1.000 Q5ZJK8 →
Q9XT06 1.000 Q9XT06 →
Q9SF16 1.000 Q9SF16 →
Q4R5G2 1.000 Q4R5G2 →
P11983 1.000 P11983 →
Q32L40 1.000 Q32L40 →
P12613 1.000 P12613 →
Q9W790 1.000 Q9W790 →
P87153 1.000 P87153 →
TCP1 T-complex protein 1 subunit alpha 1.000 landscape →
O00782 1.000 O00782 →
P18279 1.000 P18279 →
P28480 1.000 P28480 →
O15891 1.000 O15891 →
Q9N4J8 1.000 Q9N4J8 →
Q9N358 1.000 Q9N358 →
P28769 1.000 P28769 →
Q54ER7 0.998 Q54ER7 →
P42943 0.998 P42943 →
Q94757 0.997 Q94757 →
Q6LX38 0.997 Q6LX38 →
P39077 0.997 P39077 →
P54409 0.997 P54409 →
P41988 0.997 P41988 →
O94501 0.996 O94501 →
Q9V2T8 0.996 Q9V2T8 →
Q54J97 0.996 Q54J97 →