DYNC1H1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to DYNC1H1 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
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia	nan	COMPLETED
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia	nan	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
PCD New Gene Discovery	nan	COMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies	nan	RECRUITING
Mapping Disease Pathways for Biliary Atresia	nan	RECRUITING
Early Detection and Characterization of Primary Ciliary Dyskinesia	nan	UNKNOWN
Biomarker Research in Inherited Movement Disorders	nan	RECRUITING
Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies	nan	COMPLETED
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia	nan	UNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients	nan	RECRUITING
Study of Skeletal Disorders and Short Stature	nan	COMPLETED
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases	nan	COMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis.	nan	COMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk	nan	NOT_YET_RECRUITING
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials	nan	ACTIVE_NOT_RECRUITING
Inherited Reproductive Disorders	nan	RECRUITING
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia	nan	RECRUITING
Characteristics of Nondystrophic Myotonias	nan	COMPLETED
Core Stability Exercises and Hereditary Ataxia	nan	COMPLETED
Neurogenetics Patient Registry	nan	RECRUITING
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease	nan	UNKNOWN
Clinical Outcome Study for Dysferlinopathy	nan	UNKNOWN

Related proteins — ESM-2 sequence neighbours (a DYNC1H1 binder may also engage these)

Protein	Name	Similarity
Q9JHU4	—	1.000	Q9JHU4 →
P38650	—	1.000	P38650 →
P37276	—	1.000	P37276 →
P78716	—	1.000	P78716 →
P45444	—	1.000	P45444 →
Q9MBF8	—	0.999	Q9MBF8 →
Q9SMH3	—	0.998	Q9SMH3 →
F1SC07	—	0.998	F1SC07 →
P0C6F1	—	0.997	P0C6F1 →
Q9SMH5	—	0.996	Q9SMH5 →
Q63170	—	0.996	Q63170 →
Q39565	—	0.996	Q39565 →
P23098	—	0.996	P23098 →
M0R8U1	—	0.995	M0R8U1 →
Q8IVF4	—	0.995	Q8IVF4 →
Q8TE73	—	0.995	Q8TE73 →
Q39575	—	0.994	Q39575 →
Q19020	—	0.994	Q19020 →
Q27802	—	0.994	Q27802 →
Q96JB1	—	0.994	Q96JB1 →
Q22A67	—	0.993	Q22A67 →
P39057	—	0.993	P39057 →
Q96DT5	—	0.993	Q96DT5 →
Q9UFH2	—	0.993	Q9UFH2 →
Q8WXX0	—	0.993	Q8WXX0 →
Q69Z23	—	0.993	Q69Z23 →
Q91XQ0	—	0.992	Q91XQ0 →
Q8VHE6	—	0.992	Q8VHE6 →
Q19542	—	0.991	Q19542 →
Q9C0G6	—	0.991	Q9C0G6 →