PPHLN1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to PPHLN1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome	PHASE2	RECRUITING
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis.	nan	COMPLETED
Pancreatic Intraepithelial Neoplasia (PanIN) and the Association With Recurrence of Pancreatic Adenocarcinoma	nan	COMPLETED
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia	nan	UNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF)	nan	UNKNOWN
Positional Cloning of the Gene(s) Responsible for Alagille Syndrome	nan	COMPLETED
the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease.	nan	UNKNOWN
Proteomics of Primary Hyperoxaluria Type 1	nan	COMPLETED
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer	nan	COMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Analysis of Genes That Predispose People to Develop High Blood Pressure	nan	COMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism	nan	COMPLETED
Genetic Linkage Study for Hereditary Pancreatitis	nan	COMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma	nan	RECRUITING
Markers and Mechanisms of Macrovascular Disease in IDDM	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
PCD New Gene Discovery	nan	COMPLETED
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Family Blood Pressure Program - HyperGEN	nan	COMPLETED
Genetic Study of Age-Related Macular Degeneration	nan	COMPLETED
Pulmonary Hypertension--Mechanisms and Family Registry	nan	COMPLETED
Blood Proteins in Finding Pancreatic Cancer and Extrahepatic Biliary Tract Cancer	nan	COMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia	nan	COMPLETED
Study of Constitutional Platelet Disease	nan	UNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Genetic Identification (ID) of Segmental Dysplastic Nevi	nan	WITHDRAWN
Vitreous Proteomics of Patients Suffering From Pseudoexfoliation Syndrome	nan	ACTIVE_NOT_RECRUITING
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank	nan	COMPLETED
Microarray Analysis in Syndromic Obesity	nan	COMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions	nan	RECRUITING

Related proteins — ESM-2 sequence neighbours (a PPHLN1 binder may also engage these)

Protein	Name	Similarity
Q66J90	—	0.999	Q66J90 →
P97868	—	0.998	P97868 →
Q09801	—	0.995	Q09801 →
Q9D824	—	0.995	Q9D824 →
Q18221	—	0.995	Q18221 →
Q498L0	—	0.995	Q498L0 →
Q5HZJ0	—	0.995	Q5HZJ0 →
Q865B7	—	0.994	Q865B7 →
Q96GY3	—	0.994	Q96GY3 →
Q15154	—	0.994	Q15154 →
Q08D57	—	0.994	Q08D57 →
A2RUV4	—	0.994	A2RUV4 →
Q09599	—	0.994	Q09599 →
FIP1L1	Pre-mRNA 3'-end-processing factor FIP1	0.994	landscape →
Q9NRR4	—	0.994	Q9NRR4 →
F1QIC4	—	0.994	F1QIC4 →
P28220	—	0.994	P28220 →
Q5RAA7	—	0.994	Q5RAA7 →
Q27IV2	—	0.993	Q27IV2 →
Q9Y7S8	—	0.993	Q9Y7S8 →
P70047	—	0.993	P70047 →
Q3T0A6	—	0.993	Q3T0A6 →
F1Q8W0	—	0.993	F1Q8W0 →
Q86TC9	—	0.993	Q86TC9 →
B0QZF7	—	0.993	B0QZF7 →
A0A1L8HFX9	—	0.993	A0A1L8HFX9 →
Q9P1A6	—	0.992	Q9P1A6 →
Q5LJZ2	—	0.992	Q5LJZ2 →
Q1LY77	—	0.992	Q1LY77 →
Q9VR99	—	0.992	Q9VR99 →