NMRAL1 — patent landscape

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

Compound	Confidence	Supporting neighbours
SCHEMBL15569377	0.52	1/20
SCHEMBL15978916	0.45	1/20
SCHEMBL4935060	0.43	1/20
SCHEMBL4935071	0.43	1/20
SCHEMBL29846007	0.41	1/20

Clinical trials — most relevant to NMRAL1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Management of Retinitis Pigmentosa Via Combination of Wharton's Jelly-derived Mesenchymal Stem Cells and Magnovision	PHASE3	COMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization	nan	COMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
PCD New Gene Discovery	nan	COMPLETED
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants	nan	RECRUITING
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders	nan	COMPLETED
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
MRI in Autosomal Dominant Partial Epilepsy With Auditory Features	nan	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models	nan	COMPLETED
Idiopathic Dilated Cardiomyopathy	nan	COMPLETED
Stone Disease in Children and Their Families	nan	COMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans	nan	UNKNOWN
Predisposition Genes in Monogenic Diabetes (DIAMONO)	nan	COMPLETED
Genetics of Rolandic Epilepsy	nan	COMPLETED
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES)	nan	COMPLETED
Inherited Reproductive Disorders	nan	RECRUITING
Genetical Background of Non-alcoholic Fatty Liver Disease (NAFLD) in Diabetes Mellitus and in Chronic Kidney Disease	nan	UNKNOWN
the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease.	nan	UNKNOWN
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS	nan	RECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Clinical and Genetic Studies of VACTERL Association	nan	COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH)	nan	RECRUITING
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan	nan	ENROLLING_BY_INVITATION
Genomic Study of Congenital Malformation	nan	UNKNOWN
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis	nan	COMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a NMRAL1 binder may also engage these)

Protein	Name	Similarity
Q8K2T1	—	0.994	Q8K2T1 →
Q0VCN1	—	0.992	Q0VCN1 →
Q5ZID0	—	0.984	Q5ZID0 →
Q9FVQ6	—	0.978	Q9FVQ6 →
A3R052	—	0.978	A3R052 →
Q4R0H9	—	0.978	Q4R0H9 →
P0DKC8	—	0.976	P0DKC8 →
B0LL23	—	0.973	B0LL23 →
Q9SVP6	—	0.972	Q9SVP6 →
E6Y2X0	—	0.970	E6Y2X0 →
B5KRH5	—	0.968	B5KRH5 →
Q4R0I0	—	0.967	Q4R0I0 →
Q64421	—	0.966	Q64421 →
P52581	—	0.966	P52581 →
Q9D665	—	0.965	Q9D665 →
D0VWT0	—	0.964	D0VWT0 →
B6VRE8	—	0.964	B6VRE8 →
A0A221J5W8	—	0.964	A0A221J5W8 →
A0A221J5X6	—	0.962	A0A221J5X6 →
P93143	—	0.962	P93143 →
Q9LL41	—	0.961	Q9LL41 →
O46516	—	0.961	O46516 →
B2WSM8	—	0.961	B2WSM8 →
B2WSN0	—	0.960	B2WSN0 →
P27364	—	0.960	P27364 →
Q9LD00	—	0.960	Q9LD00 →
P52556	—	0.960	P52556 →
O35296	—	0.960	O35296 →
D5JWB3	—	0.959	D5JWB3 →
Q6PQJ9	—	0.959	Q6PQJ9 →