DHX36

ATP-dependent DNA/RNA helicase DHX36 · Q9H2U1 · DHX36 on Sugi Atlas →

0 patent compounds predicted against DHX36, 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 DHX36 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
Clinical Study of EBV-LMP1 Targeted DNAzyme to Treat Nasopharyngeal Carcinoma PHASE1/PHASE2COMPLETED
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Clofarabine and Cytarabine in Treating Young Patients With Refractory or Relapsed Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia PHASE1/PHASE2COMPLETED
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
A Phase I Trial of SHR3162 in Subjects With Advanced Solid Tumors PHASE1COMPLETED
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
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
A Proof of Concept Study for the DNA Repair Driven by the Mesenchymal Stem Cells in Critical COVID-19 Patients nanCOMPLETED
DDX3X Syndrome -The Seaver Autism Center for Research and Treatment is Characterizing DDX3X-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures. nanCOMPLETED
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
International PPB/DICER1 Registry nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Cause of Familial Testicular Cancer nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Genetics of Primary Ciliary Dyskinesia 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
Consortium On Risk for Early-onset Parkinson's Disease (CORE PD) nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a DHX36 binder may also engage these)

ProteinNameSimilarity
D4A2Z8 1.000 D4A2Z8 →
Q05B79 1.000 Q05B79 →
B4NBB0 1.000 B4NBB0 →
Q8VHK9 1.000 Q8VHK9 →
Q5XI69 0.999 Q5XI69 →
Q6PE54 0.999 Q6PE54 →
B3M383 0.998 B3M383 →
P20095 0.998 P20095 →
F4IDQ6 0.997 F4IDQ6 →
F4JMJ3 0.997 F4JMJ3 →
B4LX81 0.997 B4LX81 →
F4ILR7 0.997 F4ILR7 →
F4HYJ7 0.997 F4HYJ7 →
B0XDC4 0.996 B0XDC4 →
B4GEU5 0.996 B4GEU5 →
F4IM84 0.996 F4IM84 →
Q5R746 0.996 Q5R746 →
Q5R864 0.995 Q5R864 →
B2RR83 0.995 B2RR83 →
Q296Q5 0.995 Q296Q5 →
F4IJV4 0.995 F4IJV4 →
P0CE10 0.994 P0CE10 →
Q10752 0.994 Q10752 →
O45244 0.994 O45244 →
Q5RAZ4 0.994 Q5RAZ4 →
Q8VY00 0.994 Q8VY00 →
Q5BJS0 0.994 Q5BJS0 →
F4KGU4 0.993 F4KGU4 →
F4INY4 0.993 F4INY4 →
Q09530 0.993 Q09530 →