DYNC1I2 — patent landscape

Top predicted compounds (top 20 by supporting neighbours, then confidence)

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to DYNC1I2 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype	EARLY_PHASE1	COMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia	nan	COMPLETED
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies	nan	COMPLETED
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia	nan	COMPLETED
Mapping Disease Pathways for Biliary Atresia	nan	RECRUITING
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials	nan	ACTIVE_NOT_RECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies	nan	RECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Early Detection and Characterization of Primary Ciliary Dyskinesia	nan	UNKNOWN
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease	nan	UNKNOWN
Characteristics of Nondystrophic Myotonias	nan	COMPLETED
Biomarker Research in Inherited Movement Disorders	nan	RECRUITING
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk	nan	NOT_YET_RECRUITING
Inherited Reproductive Disorders	nan	RECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia	nan	UNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia	nan	RECRUITING
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases	nan	COMPLETED
Predisposition Genes in Monogenic Diabetes (DIAMONO)	nan	COMPLETED
The Relation of Microtubule-Associated Protein 2 and Cell Migration	nan	UNKNOWN
Molecular Genetic Study of Schizophrenia: Parent-Offspring Trios	nan	COMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM	nan	COMPLETED
Gyrate Atrophy Ocular and Systemic Study	nan	ACTIVE_NOT_RECRUITING

Related proteins — ESM-2 sequence neighbours (a DYNC1I2 binder may also engage these)

Protein	Name	Similarity
Q62871	—	1.000	Q62871 →
Q5NVM2	—	1.000	Q5NVM2 →
E7F6H7	—	1.000	E7F6H7 →
O88487	—	1.000	O88487 →
Q0III3	—	1.000	Q0III3 →
Q63100	—	1.000	Q63100 →
O88485	—	1.000	O88485 →
O14576	—	0.999	O14576 →
Q29RQ3	—	0.998	Q29RQ3 →
Q24246	—	0.994	Q24246 →
E9PYY5	—	0.987	E9PYY5 →
Q9UI46	—	0.986	Q9UI46 →
Q8C0M8	—	0.985	Q8C0M8 →
Q2YDS1	—	0.984	Q2YDS1 →
Q6GPB9	—	0.984	Q6GPB9 →
Q5XIL8	—	0.984	Q5XIL8 →
Q5VTH9	—	0.981	Q5VTH9 →
Q32KS2	—	0.981	Q32KS2 →
Q16959	—	0.980	Q16959 →
Q13610	—	0.979	Q13610 →
Q6PJI9	—	0.979	Q6PJI9 →
Q4V8G4	—	0.978	Q4V8G4 →
A4QNS7	—	0.978	A4QNS7 →
Q5F3K4	—	0.978	Q5F3K4 →
Q2HJ56	—	0.978	Q2HJ56 →
A6N6J5	—	0.978	A6N6J5 →
O00423	—	0.978	O00423 →
O13046	—	0.978	O13046 →
O75717	—	0.977	O75717 →
Q8C0M0	—	0.977	Q8C0M0 →