DBN1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to DBN1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
The Nutritional Supplement Phosphatidylserine in Patients With Familial Dysautonomia	PHASE2	COMPLETED
Intermittent Hypoxia Elicits Prolonged Restoration of Motor Function in Human SCI	PHASE1	COMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies	nan	RECRUITING
A Study on Risk Mutations of Vulnerability Genes of Schizophrenia	nan	UNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN)	nan	RECRUITING
Protein Synthesis in the Brain of Patients With Fragile X Syndrome	nan	COMPLETED
Biomarker Research in Inherited Movement Disorders	nan	RECRUITING
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia	nan	RECRUITING
Genes, Proteins, and Metabolites in Drug-resistant Epilepsy (DRE) Patients	nan	NOT_YET_RECRUITING
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study	nan	UNKNOWN
Identification of New FTLD Genes	nan	UNKNOWN
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models	nan	COMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies	nan	COMPLETED
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia	nan	UNKNOWN
Molecular Analysis of Patients With Neuromuscular Disease	nan	RECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
Defining the Brain Phenotype of Children With Williams Syndrome	nan	RECRUITING
The Genetic Characterization of Dementia	nan	COMPLETED
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation	nan	UNKNOWN
DNA Analysis of Tumor Tissue Samples From Patients With Diffuse Brain Stem Glioma	nan	COMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing	nan	UNKNOWN
Susceptibility Genes in Autism Spectrum Disorders	nan	COMPLETED
Nerve Ultrasound in Acquired and Genetic Sensory Neuronopathies	nan	NOT_YET_RECRUITING
Traumatic Brain Injury and Risk for Chronic Traumatic Encephalopathy	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a DBN1 binder may also engage these)

Protein	Name	Similarity
Q07266	—	1.000	Q07266 →
Q9QXS6	—	1.000	Q9QXS6 →
P18302	—	0.996	P18302 →
Q8K3I4	—	0.987	Q8K3I4 →
Q3SX22	—	0.986	Q3SX22 →
Q32LQ1	—	0.985	Q32LQ1 →
A2A9T0	—	0.985	A2A9T0 →
Q8VDP4	—	0.984	Q8VDP4 →
Q60829	—	0.983	Q60829 →
Q8R5H6	—	0.983	Q8R5H6 →
Q92558	—	0.983	Q92558 →
Q5PR69	—	0.983	Q5PR69 →
Q6P9J5	—	0.983	Q6P9J5 →
Q5NVG8	—	0.982	Q5NVG8 →
Q99LJ0	—	0.982	Q99LJ0 →
Q5BJU7	—	0.982	Q5BJU7 →
Q62418	—	0.982	Q62418 →
Q0IIJ3	—	0.981	Q0IIJ3 →
Q5R8S0	—	0.981	Q5R8S0 →
X1WE18	—	0.981	X1WE18 →
Q7TNY7	—	0.981	Q7TNY7 →
Q9QXM1	—	0.981	Q9QXM1 →
Q9Z136	—	0.981	Q9Z136 →
Q6ZQ03	—	0.981	Q6ZQ03 →
A1X157	—	0.981	A1X157 →
Q8K2L8	—	0.981	Q8K2L8 →
Q96K21	—	0.981	Q96K21 →
PPP1R1B	Protein phosphatase 1 regulatory subunit 1B	0.981	landscape →
Q6PCQ0	—	0.981	Q6PCQ0 →
Q76LL6	—	0.981	Q76LL6 →