CNOT9

CCR4-NOT transcription complex subunit 9 · Q92600 · CNOT9 on Sugi Atlas →

0 patent compounds predicted against CNOT9, 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 CNOT9 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men PHASE3ACTIVE_NOT_RECRUITING
Clinical Trial of CNCT19 Cell Injection in the Treatment of Relapsed or Refractory Acute Lymphoblastic Leukemia PHASE2RECRUITING
Phase II Clinical Trial of CNCT19 Cell Injection in the Treatment of Relapsed or Refractory Non-Hodgkin's Lymphoma PHASE2RECRUITING
A Clinical Trial of CNCT19 Cells in the Treatment of CD19 Positive Relapsed or Refractory Acute Lymphoblastic Leukemia PHASE1COMPLETED
A Clinical Trial of CNCT19 Cells in the Treatment of CD19 Positive Relapsed or Refractory Diffuse Non-Hodgkin Lymphoma PHASE1COMPLETED
A Clinical Study of Anti-CD19 Chimeric Antigen Receptor T-Cell Injection (CNCT19) in the Treatment of Cluster of Differentiation 19 (CD19) Positive Relapsed or Refractory B Cell Malignancies EARLY_PHASE1UNKNOWN
A Study of CNCT19 in the Treatment of Relapsed or Refractory Neurological Autoimmune Diseases EARLY_PHASE1RECRUITING
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay nanNOT_YET_RECRUITING
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN
Assessment Of Long Noncoding RNA CCAT1 In Colorectal Cancer Patients nanUNKNOWN
Genetic Studies Spermatogenic Failure nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections nanCOMPLETED
Genome-wide Single Cell Haplotyping as a Generic Method for Preimplantation Genetic Diagnosis nanUNKNOWN
The Genetics of Chiari Type I Malformation nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Chromosome 9 P Minus Syndrome nanRECRUITING
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
Studying The Role of Key Epigenetic Mediators in Breast Cancer Patients nanRECRUITING
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Clinical, Radiological, Histologic and Molecular Features of a Cohort of Melanocytic Tumors of the Central Nervous System nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Inherited Reproductive Disorders nanRECRUITING
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
SMYD3-Driven Metabolic Rewiring in Colorectal Liver Metastases nanNOT_YET_RECRUITING
The Value of circRNAs (hsa_circ_0004001) in Early Diagnosis of HCC nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a CNOT9 binder may also engage these)

ProteinNameSimilarity
A7MB47 1.000 A7MB47 →
Q6P819 1.000 Q6P819 →
Q6IP65 1.000 Q6IP65 →
Q9JKY0 1.000 Q9JKY0 →
Q4R347 1.000 Q4R347 →
Q5PQL2 1.000 Q5PQL2 →
Q5R6Z6 0.999 Q5R6Z6 →
Q6NWL4 0.996 Q6NWL4 →
Q92368 0.993 Q92368 →
Q9W3N6 0.978 Q9W3N6 →
Q6DGR4 0.976 Q6DGR4 →
P53829 0.975 P53829 →
Q84ZC0 0.973 Q84ZC0 →
Q16537 0.973 Q16537 →
Q6DCP6 0.973 Q6DCP6 →
P22892 0.972 P22892 →
Q68F38 0.971 Q68F38 →
Q28BM0 0.971 Q28BM0 →
A4FV68 0.971 A4FV68 →
AP1G1 AP-1 complex subunit gamma-1 0.970 landscape →
Q8N3U4 0.970 Q8N3U4 →
O04376 0.970 O04376 →
Q8CHY3 0.970 Q8CHY3 →
ATP6V1H V-type proton ATPase subunit H 0.970 landscape →
B4F766 0.970 B4F766 →
P14068 0.970 P14068 →
Q7RTS9 0.969 Q7RTS9 →
Q5ZLW3 0.969 Q5ZLW3 →
Q61151 0.969 Q61151 →
Q8LF36 0.969 Q8LF36 →