RUVBL2 — patent landscape

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

Compound	Confidence	Supporting neighbours
SCHEMBL902339	0.59	1/20
SCHEMBL15274740	0.57	1/20
SCHEMBL4725657	0.52	1/20
SCHEMBL4935332	0.52	1/20
SCHEMBL4940751	0.51	1/20
SCHEMBL15262379	0.51	1/20
SCHEMBL29748613	0.51	1/20
SCHEMBL902537	0.51	1/20
SCHEMBL902549	0.50	1/20
SCHEMBL902831	0.50	1/20
SCHEMBL902315	0.49	1/20
SCHEMBL4936715	0.48	1/20
SCHEMBL17616098	0.48	1/20
SCHEMBL15262398	0.47	1/20
SCHEMBL15277552	0.47	1/20
SCHEMBL21159309	0.46	1/20
SCHEMBL901731	0.45	1/20
SCHEMBL17616166	0.45	1/20
SCHEMBL902610	0.43	1/20
SCHEMBL26003171	0.42	1/20

Clinical trials — most relevant to RUVBL2 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
Histocompatibility Leukocyte Antigen (HLA)-A*0201 Restricted Peptide Vaccine Therapy in Patients With Gastric Cancer	PHASE1/PHASE2	COMPLETED
Histocompatibility Leukocyte Antigen (HLA)-A*0201 Restricted Peptide Vaccine Therapy in Patients With Esophageal Cancer	PHASE1/PHASE2	COMPLETED
PS-341 and Radiation to Treat Advanced Cancer of the Head and Neck	PHASE1	COMPLETED
New Biomarkers for Diagnosis and Follow-up of Patients With LRBA or CTLA4 Deficiencies	nan	UNKNOWN
Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models	nan	COMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
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
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH)	nan	RECRUITING
The Role of FGL2-FcgammaRIIB Inhibitory Pathway in Human Viral Hepatitis	nan	COMPLETED
Exome Analysis in Hearing Impaired Patients	nan	UNKNOWN
Genetic Investigation of Cancer Predisposition	nan	NOT_YET_RECRUITING
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia	nan	COMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events	nan	COMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome.	nan	COMPLETED
Studying Tissue Samples From Patients With Stage II Colon Cancer Treated on Clinical Trial CLB-9581	nan	COMPLETED
Epidemiologic, Clinical and Molecular Characteristics of Patients With Acute Respiratory Failure Affected by 2019-NCOV.	nan	UNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Autophagy in Systemic Lupus Erythematosus	nan	UNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization	nan	COMPLETED
Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Ancillary Study	nan	ACTIVE_NOT_RECRUITING
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS	nan	RECRUITING
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis	nan	UNKNOWN
Biomarkers in Tumor Samples From Younger Patients With Neuroblastoma	nan	COMPLETED
Diagnosis of Inflammatory Bowel Disease	nan	NOT_YET_RECRUITING
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism	nan	COMPLETED
A Family Study of Copy Number Variations in Patients With Autism Spectrum Disorder	nan	COMPLETED
Identification of New Candidate Genes in Patients With Mitochondrial Disease by High Resolution Chromosome Analysis on DNA Chip	nan	COMPLETED
Genetic Variants Associated With Adolescent Suicide Attempts	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a RUVBL2 binder may also engage these)

Protein	Name	Similarity
Q2TBU9	—	1.000	Q2TBU9 →
Q9WTM5	—	1.000	Q9WTM5 →
Q9DE27	—	1.000	Q9DE27 →
Q4P6N7	—	1.000	Q4P6N7 →
Q755G5	—	1.000	Q755G5 →
Q5AGZ9	—	1.000	Q5AGZ9 →
Q5BGK3	—	1.000	Q5BGK3 →
Q6C3X6	—	1.000	Q6C3X6 →
Q873C7	—	1.000	Q873C7 →
Q4WKH9	—	0.999	Q4WKH9 →
Q6CT29	—	0.999	Q6CT29 →
O94692	—	0.998	O94692 →
P0CR29	—	0.998	P0CR29 →
P0CR28	—	0.998	P0CR28 →
Q12464	—	0.998	Q12464 →
Q6FSF1	—	0.998	Q6FSF1 →
P83571	—	0.996	P83571 →
Q9VH07	—	0.996	Q9VH07 →
Q4I948	—	0.996	Q4I948 →
Q16TA2	—	0.996	Q16TA2 →
Q0IFL2	—	0.995	Q0IFL2 →
Q6CB52	—	0.995	Q6CB52 →
Q6CQA9	—	0.995	Q6CQA9 →
Q5BBV9	—	0.995	Q5BBV9 →
Q8WZS3	—	0.995	Q8WZS3 →
Q9V3K3	—	0.994	Q9V3K3 →
Q4ICA8	—	0.994	Q4ICA8 →
Q03940	—	0.994	Q03940 →
Q750R1	—	0.994	Q750R1 →
Q9GZH2	—	0.993	Q9GZH2 →