DDX1

ATP-dependent RNA helicase DDX1 · Q92499 · DDX1 on Sugi Atlas →

0 patent compounds predicted against DDX1, 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 DDX1 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
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
Clinical Study of EBV-LMP1 Targeted DNAzyme to Treat Nasopharyngeal Carcinoma PHASE1/PHASE2COMPLETED
Efficacy and Safety Assessment of Oral LBH589 in Adult Patients With Advanced Soft TIssue Sarcoma After Pre-treatment Failure PHASE2COMPLETED
Study of Individuals and Families With Aberrations in DDX41 or Similar Cancer Predisposition Variants nanRECRUITING
DDX3X Syndrome -The Seaver Autism Center for Research and Treatment is Characterizing DDX3X-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures. nanCOMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
International PPB/DICER1 Registry nanRECRUITING
A Dose-escalation Trial of Stereotactic Ablative Body Radiotherapy for Non-spine Bone & Lymph Node Oligometastates nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
ADAR1 Expression Level in Rectal Cancer nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Diamond Blackfan Anemia Registry (DBAR) nanRECRUITING
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay nanNOT_YET_RECRUITING
Phenotypes, Biomarkers and Pathophysiology in Spastic Ataxias nanUNKNOWN
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
MicroRNA-1 (miRNA-1) and MicroRNA-133a (miRNA-133a) Levels After Acute Exercise in Ultimate Frisbee Athletes nanUNKNOWN
A Proof of Concept Study for the DNA Repair Driven by the Mesenchymal Stem Cells in Critical COVID-19 Patients nanCOMPLETED
Natural History Study of FDXR Mutation-related Mitochondriopathy nanCOMPLETED
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a DDX1 binder may also engage these)

ProteinNameSimilarity
Q4R7L5 1.000 Q4R7L5 →
Q0IIK5 1.000 Q0IIK5 →
Q641Y8 1.000 Q641Y8 →
A2VD92 1.000 A2VD92 →
Q90WU3 1.000 Q90WU3 →
Q5XH91 1.000 Q5XH91 →
Q9VNV3 1.000 Q9VNV3 →
Q91VR5 0.999 Q91VR5 →
Q5NVJ8 0.999 Q5NVJ8 →
Q9V3C0 0.997 Q9V3C0 →
Q9NXZ2 0.997 Q9NXZ2 →
Q9LU46 0.996 Q9LU46 →
O74393 0.995 O74393 →
Q8GXD6 0.995 Q8GXD6 →
Q6C024 0.995 Q6C024 →
Q9C551 0.994 Q9C551 →
Q9SZB4 0.994 Q9SZB4 →
A5DGM4 0.993 A5DGM4 →
Q9DF35 0.993 Q9DF35 →
Q26696 0.993 Q26696 →
Q09775 0.993 Q09775 →
P23394 0.992 P23394 →
Q0E3X4 0.992 Q0E3X4 →
Q9H1H9 0.992 Q9H1H9 →
Q9FZ92 0.992 Q9FZ92 →
Q6CDS6 0.992 Q6CDS6 →
B4NBB0 0.992 B4NBB0 →
Q755A5 0.992 Q755A5 →
Q07886 0.992 Q07886 →
Q9DBN9 0.991 Q9DBN9 →