DYNC1LI2

Cytoplasmic dynein 1 light intermediate chain 2 · O43237 · DYNC1LI2 on Sugi Atlas →

0 patent compounds predicted against DYNC1LI2, 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 DYNC1LI2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pembrolizumab (MK-3475) in MM Patients With Residual Disease PHASE2COMPLETED
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
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia nanCOMPLETED
Early Detection and Characterization of Primary Ciliary Dyskinesia nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Inherited Reproductive Disorders nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Peripheral Neurofilament Levels and Amyotrophic Lateral Sclerosis nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Clinical Outcome Study for Dysferlinopathy nanUNKNOWN
CDH1 Germline Mutations in Lobular Breast Cancer nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Characteristics of Nondystrophic Myotonias nanCOMPLETED
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a DYNC1LI2 binder may also engage these)

ProteinNameSimilarity
Q6PDL0 1.000 Q6PDL0 →
Q5RE09 1.000 Q5RE09 →
Q4R5P6 1.000 Q4R5P6 →
Q62698 0.992 Q62698 →
Q8R1Q8 0.986 Q8R1Q8 →
Q90828 0.982 Q90828 →
Q9QXU8 0.979 Q9QXU8 →
DYNC1LI1 Cytoplasmic dynein 1 light intermediate chain 1 0.975 landscape →
Q4KUS2 0.974 Q4KUS2 →
P58405 0.971 P58405 →
O43815 0.971 O43815 →
Q9ERG2 0.970 Q9ERG2 →
Q9UPT6 0.970 Q9UPT6 →
Q9Z1N9 0.969 Q9Z1N9 →
Q13033 0.967 Q13033 →
A5D7H2 0.967 A5D7H2 →
Q9ESN9 0.967 Q9ESN9 →
Q6PAL8 0.966 Q6PAL8 →
Q9ULQ0 0.966 Q9ULQ0 →
P70483 0.966 P70483 →
Q8CC27 0.966 Q8CC27 →
Q01826 0.966 Q01826 →
Q6EDY6 0.966 Q6EDY6 →
Q9UPW8 0.965 Q9UPW8 →
Q811S7 0.965 Q811S7 →
Q803T2 0.965 Q803T2 →
O60271 0.965 O60271 →
Q0P5J8 0.965 Q0P5J8 →
Q8C079 0.965 Q8C079 →
Q5VZK9 0.965 Q5VZK9 →