BCAS2

Pre-mRNA-splicing factor SPF27 · O75934 · BCAS2 on Sugi Atlas →

0 patent compounds predicted against BCAS2, 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 BCAS2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
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
Patient's Derived Organoids for Drug Screening in Glioblastoma nanNOT_YET_RECRUITING
The Value of circRNAs (hsa_circ_0004001) in Early Diagnosis of HCC nanUNKNOWN
Genetic Variation in TRAF3IP2 (rs13190932) nanRECRUITING
Efficacy and Safety Study of EGCG/Tocotrienol in 18 Patients With Splicing-mutation-mediated Cystic Fibrosis (CF) nanCOMPLETED
SMN Circular RNAs as Potential Biomarkers for the Therapeutic Response to Nusinersen in Spinal Muscular Atrophy Patients nanUNKNOWN
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Endolymphatic Sac Tumors in a Population of Patients With Von Hippel-Lindau Disease:The Natural History and Pathobiology, and a Prospective Non-Randomized Clinical Trial of Hearing Preservation Surgery in Patients With Early Stage Endolymphatic Sac Tumors nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
Mechanisms of Cell Death in Spinal Muscular Atrophy nanCOMPLETED
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Clinical Study of Spinal Muscular Atrophy nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Analysis of Post-Translational Modifications of a Critical Protein Implicated in Amyotrophic Lateral Sclerosis nanCOMPLETED
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Home Monitoring of Adult Patients With SMA: a Pilot Multicenter Validation Study nanUNKNOWN
CDH1 Germline Mutations in Lobular Breast Cancer nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
Family Study of Melanoma in Italy nanCOMPLETED
Impact of Mutations in Aminoacyl tRNA Synthetases on Protein Translation and Cellular Stress nanWITHDRAWN
Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases nanRECRUITING
RNA Sequencing in the Framingham Heart Study Third Generation Cohort Exam 2 nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a BCAS2 binder may also engage these)

ProteinNameSimilarity
Q5RAX7 1.000 Q5RAX7 →
Q9D287 1.000 Q9D287 →
Q6PBE2 0.998 Q6PBE2 →
Q5RKQ0 0.991 Q5RKQ0 →
Q7ZXA8 0.985 Q7ZXA8 →
Q8BYR5 0.985 Q8BYR5 →
A1A5Q4 0.984 A1A5Q4 →
Q96JB5 0.984 Q96JB5 →
F4HPA7 0.984 F4HPA7 →
Q96G25 0.983 Q96G25 →
Q32KY1 0.983 Q32KY1 →
Q28DG8 0.983 Q28DG8 →
Q5ZHV2 0.983 Q5ZHV2 →
Q5REX6 0.982 Q5REX6 →
Q80TJ1 0.982 Q80TJ1 →
O57595 0.982 O57595 →
Q2TBU8 0.982 Q2TBU8 →
Q2TBK4 0.982 Q2TBK4 →
Q5RFD3 0.982 Q5RFD3 →
Q9NWB7 0.982 Q9NWB7 →
Q6GLR7 0.982 Q6GLR7 →
Q6DFL5 0.982 Q6DFL5 →
Q29RL1 0.981 Q29RL1 →
Q5FW42 0.981 Q5FW42 →
Q6DGZ3 0.981 Q6DGZ3 →
Q6DKG0 0.981 Q6DKG0 →
B1AY13 0.981 B1AY13 →
Q9R0A8 0.981 Q9R0A8 →
Q62141 0.981 Q62141 →
Q6GPR9 0.981 Q6GPR9 →