DHX30

ATP-dependent RNA helicase DHX30 · Q7L2E3 · DHX30 on Sugi Atlas →

0 patent compounds predicted against DHX30, 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 DHX30 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
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men PHASE3ACTIVE_NOT_RECRUITING
Safety Evaluation of Gene Therapy in Leber Hereditary Optic Neuropathy (LHON) Patients PHASE1/PHASE2COMPLETED
Clinical Study of EBV-LMP1 Targeted DNAzyme to Treat Nasopharyngeal Carcinoma PHASE1/PHASE2COMPLETED
Reverse Transcriptase Inhibitors in AGS 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
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
DDX3X Syndrome -The Seaver Autism Center for Research and Treatment is Characterizing DDX3X-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures. nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Stress and Treatment Response in Puerto Rican Children With Asthma nanCOMPLETED
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
International PPB/DICER1 Registry nanRECRUITING
Target of Suv420h1/2 in Hepatocytes nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Study of Constitutional Platelet Disease nanUNKNOWN
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DHX30 binder may also engage these)

ProteinNameSimilarity
Q5BJS0 1.000 Q5BJS0 →
Q5R607 1.000 Q5R607 →
Q99PU8 1.000 Q99PU8 →
Q5XI69 1.000 Q5XI69 →
Q6PE54 1.000 Q6PE54 →
Q5ZI74 1.000 Q5ZI74 →
Q2NKY8 1.000 Q2NKY8 →
F4IDQ6 1.000 F4IDQ6 →
Q5R864 0.998 Q5R864 →
D4A2Z8 0.998 D4A2Z8 →
F4HYJ7 0.998 F4HYJ7 →
F4IM84 0.998 F4IM84 →
B4NBB0 0.997 B4NBB0 →
Q5R746 0.997 Q5R746 →
B4LX81 0.997 B4LX81 →
B3M383 0.997 B3M383 →
Q8IX18 0.997 Q8IX18 →
F4INY4 0.997 F4INY4 →
P0CE10 0.995 P0CE10 →
Q3MHU3 0.995 Q3MHU3 →
Q05B79 0.995 Q05B79 →
O60231 0.995 O60231 →
F4ILR7 0.995 F4ILR7 →
Q767K6 0.995 Q767K6 →
Q8NDG6 0.995 Q8NDG6 →
Q7YR39 0.995 Q7YR39 →
F4KGU4 0.995 F4KGU4 →
B2RR83 0.994 B2RR83 →
P20095 0.994 P20095 →
P23249 0.994 P23249 →