DYNLL1

Dynein light chain 1, cytoplasmic · P63167 · DYNLL1 on Sugi Atlas →

0 patent compounds predicted against DYNLL1, 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 DYNLL1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Biologic Correlative Taxotere/AC PHASE2COMPLETED
Pembrolizumab (MK-3475) in MM Patients With Residual Disease PHASE2COMPLETED
Study of ABT-751 in Patients With Refractory Hematologic Malignancies PHASE1COMPLETED
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype EARLY_PHASE1COMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Early Detection and Characterization of Primary Ciliary Dyskinesia nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Clinical Outcome Study for Dysferlinopathy nanUNKNOWN
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Diagnostic of Chemotherapy Induced Neuropathy in Children nanCOMPLETED
PCM1-JAK2 in Therapy Related Neoplasms nanUNKNOWN
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Characteristics of Nondystrophic Myotonias nanCOMPLETED
The Impact of Mitochondrial Dysfunction on Human Bone Cell Metabolism and Remodelling nanACTIVE_NOT_RECRUITING
Primary Ciliary Dyskinesia in Adult Bronchiectasis nanNOT_YET_RECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DYNLL1 binder may also engage these)

ProteinNameSimilarity
P63168 1.000 P63168 →
P61273 1.000 P61273 →
P61285 1.000 P61285 →
P63169 1.000 P63169 →
Q24117 1.000 Q24117 →
DYNLL2 Dynein light chain 2, cytoplasmic 1.000 landscape →
O96860 1.000 O96860 →
Q9D0M5 1.000 Q9D0M5 →
Q22799 1.000 Q22799 →
O02414 1.000 O02414 →
P63170 1.000 P63170 →
Q39580 1.000 Q39580 →
Q94748 0.996 Q94748 →
Q3MHR3 0.996 Q3MHR3 →
Q78P75 0.996 Q78P75 →
Q94758 0.992 Q94758 →
Q9UR05 0.991 Q9UR05 →
O94111 0.987 O94111 →
Q86A88 0.985 Q86A88 →
Q759T0 0.985 Q759T0 →
Q02647 0.979 Q02647 →
Q6BZF8 0.978 Q6BZF8 →
Q6CWX4 0.978 Q6CWX4 →
Q6FUJ0 0.975 Q6FUJ0 →
O77210 0.968 O77210 →
PRMT5 Protein arginine N-methyltransferase 5 0.966 landscape →
P26413 0.965 P26413 →
P08418 0.965 P08418 →
Q9D0R2 0.965 Q9D0R2 →
Q9VG58 0.964 Q9VG58 →