PRPF3

U4/U6 small nuclear ribonucleoprotein Prp3 · O43395 · PRPF3 on Sugi Atlas →

1,893 patent compounds predicted against PRPF3, 1,676 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Molibresib Molibresib (SCHEMBL1872390) 1.00 1/20
Molibresib Molibresib (SCHEMBL12671490) 1.00 1/20
Molibresib Molibresib (SCHEMBL12966358) 1.00 1/20
SCHEMBL9998851 SCHEMBL9998851 0.91 1/20
SCHEMBL14756282 SCHEMBL14756282 0.88 1/20
SCHEMBL15980874 SCHEMBL15980874 0.88 1/20
SCHEMBL12966165 SCHEMBL12966165 0.87 1/20
SCHEMBL14756215 SCHEMBL14756215 0.87 1/20
SCHEMBL14756339 SCHEMBL14756339 0.87 1/20
SCHEMBL15980861 SCHEMBL15980861 0.87 1/20
SCHEMBL9998825 SCHEMBL9998825 0.86 1/20
SCHEMBL15980893 SCHEMBL15980893 0.86 1/20
SCHEMBL15980803 SCHEMBL15980803 0.86 1/20
SCHEMBL1874116 SCHEMBL1874116 0.85 1/20
SCHEMBL12671221 SCHEMBL12671221 0.85 1/20
SCHEMBL14756021 SCHEMBL14756021 0.85 1/20
SCHEMBL14756240 SCHEMBL14756240 0.85 1/20
SCHEMBL14756287 SCHEMBL14756287 0.85 1/20
SCHEMBL14756335 SCHEMBL14756335 0.85 1/20
SCHEMBL14756409 SCHEMBL14756409 0.85 1/20

Clinical trials — most relevant to PRPF3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Personalized Antisense Oligonucleotide Therapy for a Single Participant With PRPH2 Mutation Associated With Retinal Dystrophy PHASE1/PHASE2ACTIVE_NOT_RECRUITING
SAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects PHASE1COMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Natural History of PRPF31 Mutation-Associated Retinal Dystrophy nanACTIVE_NOT_RECRUITING
Clinical and Genetic Findings in Patients With PRPF31-associated Retinitis Pigmentosa nanCOMPLETED
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes nanRECRUITING
Efficacy and Safety Study of EGCG/Tocotrienol in 18 Patients With Splicing-mutation-mediated Cystic Fibrosis (CF) nanCOMPLETED
Relapsed and Progressive Sonic Hedgehog Medulloblastoma With U1 Mutation Registry Study nanRECRUITING
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
The Value of circRNAs (hsa_circ_0004001) in Early Diagnosis of HCC nanUNKNOWN
Longitudinal Study of Neurogenetic Disorders nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Differential Gene Expression of Liver Tissue and Blood From Individuals With Chronic Viral Hepatitis nanUNKNOWN
NFC Changes in SLE Patients and Its Correlation With Anti-U1RNPAntibodies and Disease Activity nanUNKNOWN
SMN Circular RNAs as Potential Biomarkers for the Therapeutic Response to Nusinersen in Spinal Muscular Atrophy Patients nanUNKNOWN
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study nanACTIVE_NOT_RECRUITING
Molecular Genetics of Retinal Degenerations nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Study of Constitutional Platelet Disease nanUNKNOWN
MicroRNA-1 (miRNA-1) and MicroRNA-133a (miRNA-133a) Levels After Acute Exercise in Ultimate Frisbee Athletes nanUNKNOWN
Nerve Ultrasound in Acquired and Genetic Sensory Neuronopathies nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a PRPF3 binder may also engage these)

ProteinNameSimilarity
Q922U1 1.000 Q922U1 →
Q5ZJ85 1.000 Q5ZJ85 →
Q5R5F1 1.000 Q5R5F1 →
Q2KIA6 1.000 Q2KIA6 →
SF3A1 Splicing factor 3A subunit 1 0.982 landscape →
P29540 0.981 P29540 →
EIF3A Eukaryotic translation initiation factor 3 subunit A 0.981 landscape →
A2VDN6 0.981 A2VDN6 →
Q1RMM1 0.981 Q1RMM1 →
Q6U6G5 0.980 Q6U6G5 →
Q40554 0.980 Q40554 →
Q8WU90 0.979 Q8WU90 →
P23116 0.978 P23116 →
Q1JU68 0.978 Q1JU68 →
Q2HJ41 0.978 Q2HJ41 →
Q6PCR7 0.978 Q6PCR7 →
Q5RAD5 0.978 Q5RAD5 →
Q8K4Z5 0.977 Q8K4Z5 →
O75391 0.977 O75391 →
A2VD00 0.977 A2VD00 →
Q5NVI3 0.976 Q5NVI3 →
Q9Z1M8 0.976 Q9Z1M8 →
O75937 0.976 O75937 →
Q3TIV5 0.976 Q3TIV5 →
Q7SYJ9 0.976 Q7SYJ9 →
SAP30BP SAP30-binding protein 0.975 landscape →
Q9JKB8 0.975 Q9JKB8 →
A4II09 0.975 A4II09 →
Q7TNE3 0.974 Q7TNE3 →
Q8BM39 0.974 Q8BM39 →