Sugi Predict

Sugi Predict / Targets / DDX20

DDX20

Probable ATP-dependent RNA helicase DDX20 · Q9UHI6 · DDX20 on Sugi Atlas →

0 patent compounds predicted against DDX20, 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 DDX20 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
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
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Target of Suv420h1/2 in Hepatocytes nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Study of Constitutional Platelet Disease nanUNKNOWN
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study nanUNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genes Associated With Development of Pulmonary Arterial Hypertension in Patients With Congenital Shunt Lesions nanRECRUITING
Cause of Familial Testicular Cancer nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Identification and Verification of Candidate Genes Responsible for Optic Disc Drusen Development nanCOMPLETED
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING

Related proteins — ESM-2 sequence neighbours (a DDX20 binder may also engage these)

ProteinNameSimilarity
Q9JJY4 — 1.000 Q9JJY4 →
P0C218 — 0.999 P0C218 →
Q2KI79 — 0.987 Q2KI79 →
O14607 — 0.983 O14607 →
E2QTD3 — 0.983 E2QTD3 →
MDM4 Protein Mdm4 0.982 landscape →
Q9Y4F3 — 0.982 Q9Y4F3 →
Q9Y4F4 — 0.982 Q9Y4F4 →
E1BZ85 — 0.982 E1BZ85 →
Q9DAU9 — 0.982 Q9DAU9 →
Q6GPJ8 — 0.982 Q6GPJ8 →
D2H3M0 — 0.981 D2H3M0 →
Q8NAT2 — 0.981 Q8NAT2 →
Q8NG08 — 0.981 Q8NG08 →
Q8S4P6 — 0.981 Q8S4P6 →
P79457 — 0.981 P79457 →
Q6P5G0 — 0.981 Q6P5G0 →
Q5R6E1 — 0.981 Q5R6E1 →
Q93ZS1 — 0.981 Q93ZS1 →
Q5VYS8 — 0.980 Q5VYS8 →
Q8C2S5 — 0.980 Q8C2S5 →
Q6ZU67 — 0.980 Q6ZU67 →
HIPK3 Homeodomain-interacting protein kinase 3 0.980 landscape →
Q96S38 — 0.980 Q96S38 →
Q588V7 — 0.980 Q588V7 →
Q53NI2 — 0.980 Q53NI2 →
Q2HJ21 — 0.980 Q2HJ21 →
Q8IZM8 — 0.980 Q8IZM8 →
Q8BJ34 — 0.980 Q8BJ34 →
Q8CIN9 — 0.980 Q8CIN9 →