NIPSNAP1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to NIPSNAP1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders	nan	RECRUITING
Non-invasive Prenatal Diagnosis of Monogenic Disorders by Linked-reads Technology	nan	COMPLETED
Non Ivasive Prenatal Diagnosis (NIPD) of Cystic Fibrosis	nan	UNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization	nan	COMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients	nan	RECRUITING
Genetic Analysis of Fraser Syndrome and Fryns Syndrome	nan	COMPLETED
Non Invasive Prenatal Testing (NIPT) of Single-gene Disorders	nan	UNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome	nan	UNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome	nan	RECRUITING
Screening for Genes in Patients With Congenital Neutropenia	nan	COMPLETED
Study of Blood Samples From High-Risk Postmenopausal Women Who Received Treatment on Breast Cancer Prevention Clinical Trials NSABP-P-1 or NSABP-P-2	nan	UNKNOWN
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk	nan	NOT_YET_RECRUITING
Genetic Investigation of Cancer Predisposition	nan	NOT_YET_RECRUITING
CoMPaSS-NMD - Computational Models for New Patients Stratification Strategies of HNMD	nan	ENROLLING_BY_INVITATION
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome.	nan	COMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions	nan	COMPLETED
Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo)	nan	WITHDRAWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives	nan	UNKNOWN
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex	nan	COMPLETED
Defining an Obesity QTL on Chromosome 3q	nan	COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Diagnosis of Prader-Willi Syndrome and Angelman Syndrome	nan	COMPLETED
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq)	nan	RECRUITING
Study of Skeletal Disorders and Short Stature	nan	COMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN)	nan	RECRUITING
Biocollection of Rare Pediatric-onset of Autoimmune and Autoinflammatory Diseases	nan	RECRUITING

Related proteins — ESM-2 sequence neighbours (a NIPSNAP1 binder may also engage these)

Protein	Name	Similarity
O55126	—	1.000	O55126 →
O55125	—	0.997	O55125 →
Q9PU58	—	0.993	Q9PU58 →
F6NVH9	—	0.993	F6NVH9 →
Q9VXK0	—	0.990	Q9VXK0 →
O75323	—	0.989	O75323 →
Q9CQE1	—	0.977	Q9CQE1 →
P34492	—	0.974	P34492 →
Q8IQ70	—	0.970	Q8IQ70 →
Q9W0S3	—	0.969	Q9W0S3 →
Q502L2	—	0.969	Q502L2 →
P0CU76	—	0.969	P0CU76 →
Q9LW26	—	0.969	Q9LW26 →
Q61CA3	—	0.969	Q61CA3 →
Q562B5	—	0.969	Q562B5 →
Q8BX10	—	0.969	Q8BX10 →
Q54I58	—	0.969	Q54I58 →
C5D9S7	—	0.968	C5D9S7 →
F4J8C6	—	0.968	F4J8C6 →
A0AKL8	—	0.967	A0AKL8 →
Q9CQN1	—	0.967	Q9CQN1 →
Q5FWM4	—	0.967	Q5FWM4 →
B4PY69	—	0.967	B4PY69 →
PGAM5	Serine/threonine-protein phosphatase PGAM5, mitochondrial	0.967	landscape →
P0DY54	—	0.967	P0DY54 →
Q9QX60	—	0.967	Q9QX60 →
Q8NXW5	—	0.967	Q8NXW5 →
A6TZ65	—	0.966	A6TZ65 →
Q84WW3	—	0.966	Q84WW3 →
A0A2I1C3W7	—	0.966	A0A2I1C3W7 →