Sugi Predict

Sugi Predict / Targets / DCTN1

DCTN1

Dynactin subunit 1 · Q14203 · DCTN1 on Sugi Atlas →

0 patent compounds predicted against DCTN1, 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 DCTN1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Phase 3 Study Of OCU400 Gene Therapy for the Treatment Of Retinitis Pigmentosa PHASE3ACTIVE_NOT_RECRUITING
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype EARLY_PHASE1COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Identification (ID) of Segmental Dysplastic Nevi nanWITHDRAWN
Dentatorubral-pallidoluysian Atrophy Natural History and Biomarkers Study nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Early Detection and Characterization of Primary Ciliary Dyskinesia nanUNKNOWN
Molecular Analysis of Patients With Neuromuscular Disease nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Inherited Reproductive Disorders nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Gait in Rare Diseases nanCOMPLETED
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases nanCOMPLETED
Magnetic Resonance Imaging for Improving Knowledge of Brain Tumor Biology in Patients With Resectable Glioblastoma nanRECRUITING
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DCTN1 binder may also engage these)

ProteinNameSimilarity
O08788 — 1.000 O08788 →
A0A287B8J2 — 1.000 A0A287B8J2 →
P28023 — 1.000 P28023 →
Q6PCJ1 — 1.000 Q6PCJ1 →
P35458 — 1.000 P35458 →
P13496 — 1.000 P13496 →
Q2KN95 — 0.997 Q2KN95 →
O55156 — 0.996 O55156 →
A6QR54 — 0.995 A6QR54 →
Q9W0M1 — 0.995 Q9W0M1 →
Q5B993 — 0.995 Q5B993 →
Q09350 — 0.994 Q09350 →
Q7YS99 — 0.994 Q7YS99 →
Q75EN7 — 0.994 Q75EN7 →
Q750P7 — 0.994 Q750P7 →
A8WUP2 — 0.994 A8WUP2 →
Q8SWR2 — 0.994 Q8SWR2 →
Q292S8 — 0.993 Q292S8 →
Q8BVL9 — 0.993 Q8BVL9 →
Q96N16 — 0.993 Q96N16 →
Q23529 — 0.993 Q23529 →
Q9NSC5 — 0.993 Q9NSC5 →
Q9UDT6 — 0.992 Q9UDT6 →
Q75EZ7 — 0.992 Q75EZ7 →
O15083 — 0.992 O15083 →
C5E2E7 — 0.992 C5E2E7 →
Q2KN94 — 0.992 Q2KN94 →
Q01397 — 0.992 Q01397 →
Q9FHY8 — 0.992 Q9FHY8 →
Q9LEZ4 — 0.992 Q9LEZ4 →