RER1 — patent landscape

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

Compound	Confidence	Supporting neighbours
SCHEMBL4699731	1.00	2/20
SCHEMBL16111548	1.00	2/20
SCHEMBL29358745	1.00	2/20
SCHEMBL29380618	1.00	2/20
SCHEMBL29931136	1.00	2/20
SCHEMBL4697866	0.89	2/20
SCHEMBL24532075	0.89	2/20
SCHEMBL4697696	0.86	2/20
SCHEMBL23092285	0.86	2/20
SCHEMBL29688472	0.86	2/20
SCHEMBL22024695	0.86	2/20
SCHEMBL16136600	0.84	2/20
SCHEMBL24532058	0.83	2/20
SCHEMBL22025026	0.82	2/20
SCHEMBL22119546	0.82	2/20
SCHEMBL24532062	0.82	2/20
SCHEMBL18804561	0.81	2/20
SCHEMBL22024561	0.81	2/20
SCHEMBL22025030	0.81	2/20
SCHEMBL24532038	0.81	2/20

Clinical trials — most relevant to RER1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Cystagon to Treat Infantile Neuronal Ceroid Lipofuscinosis	PHASE4	COMPLETED
Betaine and Peroxisome Biogenesis Disorders	PHASE3	COMPLETED
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer	PHASE2	UNKNOWN
Targeting Endoplasmic Reticulum Stress in Human Hypertension	PHASE1/PHASE2	RECRUITING
Novel Peptide Vaccination for Patients With Advanced Bladder Cancer	PHASE1	COMPLETED
Breakpoint Analysis of de Novo Apparently Balanced Chromosomal Translocations	EARLY_PHASE1	COMPLETED
Quantification of GADD34 Expression in RA	nan	COMPLETED
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models	nan	COMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics	nan	UNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
Genetics of Rolandic Epilepsy	nan	COMPLETED
Clinical and Basic Research on the Necessity of Scar Tissue Resection During Intrauterine Adhesions	nan	UNKNOWN
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study	nan	UNKNOWN
Neurogenetics Patient Registry	nan	RECRUITING
Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate	nan	RECRUITING
Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC)	nan	RECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome	nan	UNKNOWN
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes	nan	RECRUITING
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants	nan	RECRUITING
Sodium Transport: Genetics and Hypertension	nan	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
Chronic Cough and CANVAS (Cerebellar Ataxia With Neuropathy and Bilateral Vestibular Areflexia Syndrome)	nan	COMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants.	nan	UNKNOWN
MERC Proteins in Saliva and GCF in Periodontal Disease (ELISA Study)	nan	COMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia	nan	NOT_YET_RECRUITING
Diagnosis of Inflammatory Bowel Disease	nan	NOT_YET_RECRUITING
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Von Hippel-Lindau (VHL): Clinical Manifestations, Diagnosis, Management and Molecular Bases of Inherited Renal and Other Urologic Malignant Disorders	nan	RECRUITING
Rolandic Epilepsy Genomewide Association International Study	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a RER1 binder may also engage these)

Protein	Name	Similarity
Q9CQU3	—	1.000	Q9CQU3 →
Q5R5U4	—	1.000	Q5R5U4 →
A5PJ65	—	1.000	A5PJ65 →
Q498C8	—	1.000	Q498C8 →
Q5ZHM5	—	1.000	Q5ZHM5 →
Q1KZ54	—	1.000	Q1KZ54 →
P52879	—	1.000	P52879 →
O48670	—	0.999	O48670 →
P04124	—	0.998	P04124 →
Q77ZL5	—	0.998	Q77ZL5 →
Q77ZK8	—	0.998	Q77ZK8 →
Q1KXU2	—	0.998	Q1KXU2 →
P05779	—	0.997	P05779 →
Q67205	—	0.997	Q67205 →
Q77MS4	—	0.997	Q77MS4 →
P18033	—	0.997	P18033 →
P34395	—	0.997	P34395 →
Q6XT33	—	0.997	Q6XT33 →
P0DOF8	—	0.997	P0DOF8 →
P0DOF5	—	0.997	P0DOF5 →
A8C8W4	—	0.996	A8C8W4 →
Q1XD96	—	0.996	Q1XD96 →
P51391	—	0.996	P51391 →
P75083	—	0.996	P75083 →
P84392	—	0.996	P84392 →
Q10358	—	0.996	Q10358 →
P02657	—	0.996	P02657 →
Q76V12	—	0.996	Q76V12 →
Q89687	—	0.996	Q89687 →
Q7V4Q2	—	0.996	Q7V4Q2 →