NOP10

H/ACA ribonucleoprotein complex subunit 3 · Q9NPE3 · NOP10 on Sugi Atlas →

0 patent compounds predicted against NOP10, 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 NOP10 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
ONC201 in Recurrent/Refractory Metastatic Breast Cancer and Advanced Endometrial Carcinoma PHASE2COMPLETED
[C-11]NOP-1A and Alcohol Use Disorder EARLY_PHASE1COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Micro Ribosomal Nucleic Acid 155 in Non Hodgkin Lymphoma nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Study of Specimens From Young Patients With Neuroblastoma nanCOMPLETED
Prospective Genetic Study in Patients With Ovarian Insufficiency nanUNKNOWN
Mechanisms of Cell Death in Spinal Muscular Atrophy nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Characteristics of Idiopathic Familial Voice Disorders nanCOMPLETED
iPSC Neurons From Adult Survivors of Childhood Cancer Who Have Persistent Vincristine-Induced Neuropathy nanCOMPLETED
Cyclosporin A Therapy in Childhood Nephrotic Syndrome nanUNKNOWN
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Blood Sample Donations to Study the Role of Genes in Pain nanCOMPLETED
B3 for NMD: Bench to Bedside and Back nanENROLLING_BY_INVITATION
Expression Pattern of HNRNPH1 and HNRNPK Genes in MPNs nanUNKNOWN
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Investigation of Copy Number Variations and Genetic Variants in POI nanRECRUITING
Impact of Weight Loss on the Human Sperm Epitranscriptome nanACTIVE_NOT_RECRUITING
Inspiratory Muscle Training in Nemaline Myopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NOP10 binder may also engage these)

ProteinNameSimilarity
Q9CQS2 1.000 Q9CQS2 →
Q9P7M5 0.998 Q9P7M5 →
O83952 0.998 O83952 →
Q6BQP3 0.998 Q6BQP3 →
B8GV54 0.997 B8GV54 →
Q6CSZ0 0.997 Q6CSZ0 →
Q93XX8 0.996 Q93XX8 →
P83864 0.996 P83864 →
Q5SD12 0.996 Q5SD12 →
Q9V5P6 0.996 Q9V5P6 →
P07718 0.995 P07718 →
Q971I1 0.995 Q971I1 →
Q0ZIX8 0.995 Q0ZIX8 →
Q08259 0.995 Q08259 →
B0VQS2 0.995 B0VQS2 →
A0T0I2 0.995 A0T0I2 →
A8SEE4 0.995 A8SEE4 →
Q54J26 0.994 Q54J26 →
A4QKX5 0.994 A4QKX5 →
A4QKN2 0.994 A4QKN2 →
Q0ATU3 0.994 Q0ATU3 →
Q8E3W3 0.994 Q8E3W3 →
P55759 0.994 P55759 →
Q7CQJ0 0.993 Q7CQJ0 →
Q5PHY6 0.993 Q5PHY6 →
Q8P2C7 0.993 Q8P2C7 →
P08230 0.993 P08230 →
Q5GSU8 0.993 Q5GSU8 →
P0DTB5 0.993 P0DTB5 →
Q06450 0.993 Q06450 →