DDX17

Probable ATP-dependent RNA helicase DDX17 · Q92841 · DDX17 on Sugi Atlas →

0 patent compounds predicted against DDX17, 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 DDX17 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
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
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100 PHASE1/PHASE2COMPLETED
Study of Individuals and Families With Aberrations in DDX41 or Similar Cancer Predisposition Variants nanRECRUITING
Studying Chromosomes in Samples From Younger Patients With Neuroblastoma nanCOMPLETED
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
Cause of Familial Testicular Cancer nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
International PPB/DICER1 Registry nanRECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare Diseases nanUNKNOWN
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Molecular Basis of Pediatric Liver Cancer nanRECRUITING
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Natural History Study of Smith-Magenis Syndrome nanACTIVE_NOT_RECRUITING
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Screening for Early Pancreatic Neoplasia (Cancer of the Pancreas Screening or CAPS4 Study) nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a DDX17 binder may also engage these)

ProteinNameSimilarity
Q501J6 0.994 Q501J6 →
A5A6J2 0.993 A5A6J2 →
DDX5 Probable ATP-dependent RNA helicase DDX5 0.992 landscape →
Q5N7W4 0.992 Q5N7W4 →
Q9LYJ9 0.992 Q9LYJ9 →
Q61656 0.991 Q61656 →
P19109 0.991 P19109 →
Q75HJ0 0.991 Q75HJ0 →
Q4R6M5 0.991 Q4R6M5 →
A6R3L3 0.990 A6R3L3 →
Q26696 0.990 Q26696 →
Q61496 0.990 Q61496 →
A6RJA2 0.990 A6RJA2 →
Q8H136 0.990 Q8H136 →
Q5R4I9 0.990 Q5R4I9 →
P0CQ75 0.989 P0CQ75 →
P0CQ74 0.989 P0CQ74 →
Q4P733 0.989 Q4P733 →
Q8W4R3 0.989 Q8W4R3 →
P0CQ89 0.988 P0CQ89 →
P0CQ88 0.988 P0CQ88 →
Q10MH8 0.988 Q10MH8 →
Q09530 0.988 Q09530 →
Q4I7F9 0.987 Q4I7F9 →
A3LQ01 0.987 A3LQ01 →
Q5F485 0.987 Q5F485 →
Q0DB53 0.987 Q0DB53 →
Q62167 0.987 Q62167 →
Q6C024 0.987 Q6C024 →
A4RK80 0.987 A4RK80 →