PBDC1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to PBDC1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Betaine and Peroxisome Biogenesis Disorders	PHASE3	COMPLETED
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome	PHASE2	RECRUITING
Breakpoint Analysis of de Novo Apparently Balanced Chromosomal Translocations	EARLY_PHASE1	COMPLETED
Mapping Disease Pathways for Biliary Atresia	nan	RECRUITING
Biliary Atresia Study in Infants and Children	nan	RECRUITING
PCD New Gene Discovery	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Development of a New Immunochemistry Method Using Antibodies of Proteins Related Bile Duct Cancer	nan	COMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma	nan	RECRUITING
Genomic Study of Congenital Malformation	nan	UNKNOWN
Mayo AVC Registry and Biobank	nan	RECRUITING
Family Studies in Primary Biliary Cirrhosis (PBC)	nan	UNKNOWN
Chest Wall Deformities in Children - Epidemiological Data	nan	COMPLETED
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer	nan	COMPLETED
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders	nan	COMPLETED
Aberrant Gene Expression Prostate Carcinoma	nan	ACTIVE_NOT_RECRUITING
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s)	nan	COMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Shanghai High Myopia Study	nan	RECRUITING
Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes	nan	RECRUITING
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms	nan	UNKNOWN
Von Hippel-Lindau (VHL): Clinical Manifestations, Diagnosis, Management and Molecular Bases of Inherited Renal and Other Urologic Malignant Disorders	nan	RECRUITING
Hereditary Nonpolyposis Colorectal Cancer in Taiwan-Related Genetic Study and Clinical Applications	nan	UNKNOWN
Pediatric Evaluation and Registry for Liver Cholestasis in Canada	nan	RECRUITING
Genetic Diagnosis in Congenital Cataracts	nan	COMPLETED
Analysis of Genes That Predispose People to Develop High Blood Pressure	nan	COMPLETED
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples	nan	COMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions	nan	RECRUITING
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science	nan	RECRUITING

Related proteins — ESM-2 sequence neighbours (a PBDC1 binder may also engage these)

Protein	Name	Similarity
Q9D0B6	—	0.997	Q9D0B6 →
P0DQH9	—	0.991	P0DQH9 →
P0C569	—	0.989	P0C569 →
A0A2B4SJZ1	—	0.989	A0A2B4SJZ1 →
Q9D992	—	0.989	Q9D992 →
Q5EP34	—	0.989	Q5EP34 →
P12601	—	0.988	P12601 →
Q0A452	—	0.988	Q0A452 →
Q2H137	—	0.988	Q2H137 →
Q9QBY9	—	0.988	Q9QBY9 →
Q8QPG0	—	0.988	Q8QPG0 →
Q9EXD5	—	0.988	Q9EXD5 →
Q9QBZ3	—	0.988	Q9QBZ3 →
Q9AXU3	—	0.988	Q9AXU3 →
Q9WH76	—	0.988	Q9WH76 →
P13778	—	0.988	P13778 →
P24741	—	0.988	P24741 →
Q2F4H0	—	0.988	Q2F4H0 →
B4QT24	—	0.988	B4QT24 →
Q6DNX7	—	0.988	Q6DNX7 →
P46984	—	0.988	P46984 →
Q0A2K9	—	0.988	Q0A2K9 →
Q2VC91	—	0.988	Q2VC91 →
Q5RDL5	—	0.988	Q5RDL5 →
O59835	—	0.987	O59835 →
A4U6V9	—	0.987	A4U6V9 →
Q5VKP5	—	0.987	Q5VKP5 →
Q85450	—	0.987	Q85450 →
Q09159	—	0.987	Q09159 →
BCCIP	BRCA2 and CDKN1A-interacting protein	0.987	landscape →