RBM22

Pre-mRNA-splicing factor RBM22 · Q9NW64 · RBM22 on Sugi Atlas →

0 patent compounds predicted against RBM22, 0 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to RBM22 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Phase I/II Study to Evaluate a SARS-CoV-2 mRNA Vaccine in Healthy Adults PHASE1/PHASE2COMPLETED
Evaluate the Safety and Immunogenicity of a SARS-CoV-2 mRNA Vaccine Booster PHASE1COMPLETED
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
SMN Circular RNAs as Potential Biomarkers for the Therapeutic Response to Nusinersen in Spinal Muscular Atrophy Patients nanUNKNOWN
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
Efficacy and Safety Study of EGCG/Tocotrienol in 18 Patients With Splicing-mutation-mediated Cystic Fibrosis (CF) nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
SRSF2 Gene Mutation in Patients With t-MDS/AML nanCOMPLETED
Research for Individualized Therapeutics in Rare Genetic Disease nanENROLLING_BY_INVITATION
Genetic and Environmental Risk Factors for Hemorrhagic Stroke nanRECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases nanRECRUITING
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders nanCOMPLETED
Expression Pattern of HNRNPH1 and HNRNPK Genes in MPNs nanUNKNOWN
Becker Muscular Dystrophy - A Natural History Study to Predict Efficacy of Exon Skipping nanUNKNOWN
Transcriptomic Analysis of Fibroblasts and Blood in Patients With Rare Diseases nanRECRUITING
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Immunophenotyping and Xist Gene in AML nanUNKNOWN
Studying Genes in Samples From Younger Patients With Desmoplastic Small Round Cell Tumor Registered on COG-D9902 or COG-ABTR01B1 nanCOMPLETED
Mechanisms of Cell Death in Spinal Muscular Atrophy nanCOMPLETED
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
STRucturation of Transcript Analysis of Genes Involved in Hereditary Cancers nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Natural History Characterization in Symptomatic and Asymptomatic Progranuline Gene Mutation Carriers nanCOMPLETED
MYO-SHARE: MYO-MRI in Neuromuscular Diseases nanENROLLING_BY_INVITATION
Study of Individuals and Families With Aberrations in DDX41 or Similar Cancer Predisposition Variants nanRECRUITING
Patient's Derived Organoids for Drug Screening in Glioblastoma nanNOT_YET_RECRUITING
Precision Diagnosis and Therapy for Rare Diseases by Interpreting Non-coding Genomes nanRECRUITING
Home Monitoring of Adult Patients With SMA: a Pilot Multicenter Validation Study nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a RBM22 binder may also engage these)

ProteinNameSimilarity
Q4R4J1 1.000 Q4R4J1 →
Q8BHS3 1.000 Q8BHS3 →
Q5ZM16 1.000 Q5ZM16 →
Q5RAY5 1.000 Q5RAY5 →
Q4V7D7 1.000 Q4V7D7 →
Q3B7L8 1.000 Q3B7L8 →
Q6P616 1.000 Q6P616 →
Q7ZXB5 1.000 Q7ZXB5 →
Q6NZZ9 1.000 Q6NZZ9 →
Q5AX35 0.993 Q5AX35 →
Q9LNV5 0.992 Q9LNV5 →
Q6Z358 0.992 Q6Z358 →
Q5SNN4 0.991 Q5SNN4 →
O59800 0.990 O59800 →
Q8TC92 0.990 Q8TC92 →
Q9ZW36 0.990 Q9ZW36 →
P35728 0.989 P35728 →
A8NS61 0.989 A8NS61 →
Q8BHR2 0.988 Q8BHR2 →
Q7SH49 0.988 Q7SH49 →
P0CR50 0.988 P0CR50 →
Q9FL40 0.988 Q9FL40 →
Q07205 0.988 Q07205 →
Q28E45 0.987 Q28E45 →
P0CR14 0.987 P0CR14 →
Q6DJI8 0.987 Q6DJI8 →
P87253 0.987 P87253 →
P0CR51 0.987 P0CR51 →
Q4W9V0 0.987 Q4W9V0 →
Q966L5 0.987 Q966L5 →