DDX6

Probable ATP-dependent RNA helicase DDX6 · P26196 · DDX6 on Sugi Atlas →

1,672 patent compounds predicted against DDX6, 1,463 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours
Azd-6482 Azd-6482 (SCHEMBL825695) 1.00 1/20
Azd-6482 Azd-6482 (SCHEMBL1812377) 1.00 1/20
Azd-6482 Azd-6482 (SCHEMBL4353531) 1.00 1/20
SCHEMBL26137372 SCHEMBL26137372 0.85 1/20
SCHEMBL26137495 SCHEMBL26137495 0.85 1/20
SCHEMBL909768 SCHEMBL909768 0.84 1/20
SCHEMBL4348187 SCHEMBL4348187 0.84 1/20
SCHEMBL4348197 SCHEMBL4348197 0.84 1/20
SCHEMBL25359198 SCHEMBL25359198 0.84 1/20
SCHEMBL25952290 SCHEMBL25952290 0.84 1/20
SCHEMBL27116153 SCHEMBL27116153 0.84 1/20
SCHEMBL26136961 SCHEMBL26136961 0.81 1/20
SCHEMBL26136962 SCHEMBL26136962 0.81 1/20
SCHEMBL27116441 SCHEMBL27116441 0.81 1/20
SCHEMBL25414825 SCHEMBL25414825 0.80 1/20
SCHEMBL25414829 SCHEMBL25414829 0.80 1/20
SCHEMBL25415273 SCHEMBL25415273 0.80 1/20
SCHEMBL25415277 SCHEMBL25415277 0.80 1/20
SCHEMBL26136960 SCHEMBL26136960 0.80 1/20
SCHEMBL26137362 SCHEMBL26137362 0.80 1/20

Clinical trials — most relevant to DDX6 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Pharmacogenetics of Disulfiram for Cocaine 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
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Screening for Early Pancreatic Neoplasia (Cancer of the Pancreas Screening or CAPS4 Study) nanCOMPLETED
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay nanNOT_YET_RECRUITING
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
The Genetic Study of Primary Angle-Closure Glaucoma nanUNKNOWN
Germline Mutations in Pancreatic Adenocarcinoma nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Secretin-Stimulated Magnetic Resonance Cholangiopancreatography (S-MRCP) in Pancreatic Patients nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Prospective Study to Assess Medical Performance of Optical Mapping and Long Read Sequencing in Detecting Numerical and Structural Chromosome Abnormalities nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Diagnostic Research in Patients With Rare Diseases - Solving the Unsolved Rare Diseases nanUNKNOWN
Genetic Testing in Detection of Late-Onset Hearing Loss nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Cause of Familial Testicular Cancer nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
A Study of the Genetic Analysis of Brain Disorders nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DDX6 binder may also engage these)

ProteinNameSimilarity
Q5ZKB9 1.000 Q5ZKB9 →
Q5RFQ5 1.000 Q5RFQ5 →
Q9WTM2 1.000 Q9WTM2 →
Q0IHV9 1.000 Q0IHV9 →
P54824 1.000 P54824 →
A7TGU7 0.999 A7TGU7 →
P54823 0.999 P54823 →
Q7XMK8 0.997 Q7XMK8 →
Q09181 0.997 Q09181 →
Q9M2E0 0.997 Q9M2E0 →
Q94BV4 0.996 Q94BV4 →
Q75BS4 0.996 Q75BS4 →
Q4HW67 0.994 Q4HW67 →
Q8RXK6 0.993 Q8RXK6 →
A6ZXG9 0.993 A6ZXG9 →
P39517 0.993 P39517 →
Q54TF8 0.993 Q54TF8 →
Q54E49 0.992 Q54E49 →
A3LWX3 0.992 A3LWX3 →
Q0U7S9 0.992 Q0U7S9 →
O13792 0.992 O13792 →
A3LNL1 0.992 A3LNL1 →
Q6CSZ7 0.991 Q6CSZ7 →
A2QY39 0.991 A2QY39 →
A4R715 0.991 A4R715 →
Q6H7S2 0.991 Q6H7S2 →
Q6FQU5 0.991 Q6FQU5 →
Q4WWD3 0.991 Q4WWD3 →
Q0CBE1 0.991 Q0CBE1 →
A1CJ18 0.991 A1CJ18 →