DHX35

Probable ATP-dependent RNA helicase DHX35 · Q9H5Z1 · DHX35 on Sugi Atlas →

0 patent compounds predicted against DHX35, 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 DHX35 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Clofarabine and Cytarabine in Treating Young Patients With Refractory or Relapsed Acute Myeloid Leukemia or Acute Lymphoblastic Leukemia PHASE1/PHASE2COMPLETED
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
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
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
CoMPaSS-NMD - Computational Models for New Patients Stratification Strategies of HNMD nanENROLLING_BY_INVITATION
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Study of Constitutional Platelet Disease nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Cause of Familial Testicular Cancer nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
A Proof of Concept Study for the DNA Repair Driven by the Mesenchymal Stem Cells in Critical COVID-19 Patients nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Genes Associated With Development of Pulmonary Arterial Hypertension in Patients With Congenital Shunt Lesions nanRECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Hereditary Nonpolyposis Colorectal Cancer in Taiwan-Related Genetic Study and Clinical Applications nanUNKNOWN
Identification of New Colorectal Cancer Genes nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DHX35 binder may also engage these)

ProteinNameSimilarity
Q5RBD4 1.000 Q5RBD4 →
Q80VY9 1.000 Q80VY9 →
Q9BKQ8 1.000 Q9BKQ8 →
Q5RAZ4 0.999 Q5RAZ4 →
Q9H6R0 0.999 Q9H6R0 →
O22899 0.997 O22899 →
O17438 0.997 O17438 →
Q5XI69 0.997 Q5XI69 →
Q7K3M5 0.996 Q7K3M5 →
O35286 0.996 O35286 →
DHX15 ATP-dependent RNA helicase DHX15 0.995 landscape →
B0XDC4 0.995 B0XDC4 →
Q6PE54 0.995 Q6PE54 →
Q9LZQ9 0.994 Q9LZQ9 →
Q03319 0.994 Q03319 →
F4JRJ6 0.994 F4JRJ6 →
Q20875 0.994 Q20875 →
F4IE66 0.993 F4IE66 →
O42945 0.992 O42945 →
Q5R864 0.992 Q5R864 →
B4NBB0 0.992 B4NBB0 →
Q8IX18 0.992 Q8IX18 →
P36009 0.992 P36009 →
Q54NJ4 0.991 Q54NJ4 →
Q22307 0.991 Q22307 →
F4ILR7 0.990 F4ILR7 →
B3M383 0.990 B3M383 →
F4IDQ6 0.990 F4IDQ6 →
Q93Y16 0.990 Q93Y16 →
B4LX81 0.989 B4LX81 →