Sugi Predict

Sugi Predict / Targets / DCTN3

DCTN3

Dynactin subunit 3 · O75935 · DCTN3 on Sugi Atlas →

0 patent compounds predicted against DCTN3, 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 DCTN3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
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
Inherited Reproductive Disorders nanRECRUITING
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Early Detection and Characterization of Primary Ciliary Dyskinesia nanUNKNOWN
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases nanCOMPLETED
Genetic Identification (ID) of Segmental Dysplastic Nevi nanWITHDRAWN
Gait in Rare Diseases nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Nerve Ultrasound in Acquired and Genetic Sensory Neuronopathies nanNOT_YET_RECRUITING
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Primary Ciliary Dyskinesia in Adult Bronchiectasis nanNOT_YET_RECRUITING
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Gene Analysis of Parkinson's Disease nanCOMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a DCTN3 binder may also engage these)

ProteinNameSimilarity
Q9Z0Y1 — 1.000 Q9Z0Y1 →
F1SEC0 — 1.000 F1SEC0 →
Q0P5A1 — 1.000 Q0P5A1 →
Q09248 — 0.993 Q09248 →
Q1HQF2 — 0.992 Q1HQF2 →
Q7K2D2 — 0.991 Q7K2D2 →
Q9GYU7 — 0.990 Q9GYU7 →
Q9U2Y2 — 0.990 Q9U2Y2 →
Q9W5P1 — 0.990 Q9W5P1 →
Q28Y46 — 0.990 Q28Y46 →
P45966 — 0.989 P45966 →
Q7PZ25 — 0.989 Q7PZ25 →
Q0WQE7 — 0.988 Q0WQE7 →
Q7S8C2 — 0.988 Q7S8C2 →
Q3ZCF2 — 0.987 Q3ZCF2 →
PSME2 Proteasome activator complex subunit 2 0.987 landscape →
Q9CXU0 — 0.987 Q9CXU0 →
Q6IP67 — 0.987 Q6IP67 →
Q9USV3 — 0.987 Q9USV3 →
Q9BTT4 — 0.987 Q9BTT4 →
Q5E9G3 — 0.987 Q5E9G3 →
Q8LDS5 — 0.987 Q8LDS5 →
Q7Q5R5 — 0.986 Q7Q5R5 →
Q6DJ25 — 0.986 Q6DJ25 →
P97372 — 0.986 P97372 →
Q863Z0 — 0.986 Q863Z0 →
P47149 — 0.986 P47149 →
C0LU16 — 0.986 C0LU16 →
Q9MBF8 — 0.986 Q9MBF8 →
O14777 — 0.985 O14777 →