DDX18

ATP-dependent RNA helicase DDX18 · Q9NVP1 · DDX18 on Sugi Atlas →

0 patent compounds predicted against DDX18, 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 DDX18 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Long Term Extension Study in Patients With Primary Hyperoxaluria PHASE3ACTIVE_NOT_RECRUITING
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Clinical Study of EBV-LMP1 Targeted DNAzyme to Treat Nasopharyngeal Carcinoma PHASE1/PHASE2COMPLETED
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
Study of Individuals and Families With Aberrations in DDX41 or Similar Cancer Predisposition Variants nanRECRUITING
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
DDX3X Syndrome -The Seaver Autism Center for Research and Treatment is Characterizing DDX3X-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures. nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
International PPB/DICER1 Registry nanRECRUITING
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
ADAR1 Expression Level in Rectal Cancer nanRECRUITING
A Dose-escalation Trial of Stereotactic Ablative Body Radiotherapy for Non-spine Bone & Lymph Node Oligometastates nanCOMPLETED
Effect of Periodontal Treatment on Inflammasome Proteins in Periodontal Diseases nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
A Proof of Concept Study for the DNA Repair Driven by the Mesenchymal Stem Cells in Critical COVID-19 Patients nanCOMPLETED
Diamond Blackfan Anemia Registry (DBAR) nanRECRUITING
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay nanNOT_YET_RECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
International Ataxia Rating Scale in Younger Patients nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Chromosome 18 Clinical Research Center nanRECRUITING
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study nanACTIVE_NOT_RECRUITING
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DDX18 binder may also engage these)

ProteinNameSimilarity
Q8K363 0.999 Q8K363 →
Q9SB89 0.995 Q9SB89 →
Q9LIH9 0.995 Q9LIH9 →
Q0D622 0.993 Q0D622 →
O74393 0.993 O74393 →
Q9UTP9 0.992 Q9UTP9 →
Q1EA54 0.991 Q1EA54 →
Q5BBY1 0.991 Q5BBY1 →
Q9DF36 0.991 Q9DF36 →
Q9VD51 0.991 Q9VD51 →
Q0DLB9 0.991 Q0DLB9 →
A5E3K3 0.991 A5E3K3 →
Q6BXG0 0.990 Q6BXG0 →
Q4WQM4 0.989 Q4WQM4 →
D3ZA12 0.989 D3ZA12 →
Q9FFT9 0.989 Q9FFT9 →
Q0DBS1 0.989 Q0DBS1 →
A1CW14 0.989 A1CW14 →
Q6FPT7 0.989 Q6FPT7 →
Q8GXD6 0.988 Q8GXD6 →
A5DGM4 0.988 A5DGM4 →
Q6CGD1 0.988 Q6CGD1 →
Q75C76 0.988 Q75C76 →
A4R8B5 0.988 A4R8B5 →
A3KFM7 0.988 A3KFM7 →
Q5ZLN8 0.988 Q5ZLN8 →
Q7XJN0 0.988 Q7XJN0 →
Q2NL08 0.988 Q2NL08 →
Q6BH93 0.988 Q6BH93 →
P40562 0.988 P40562 →