CWC27

Spliceosome-associated protein CWC27 homolog · Q6UX04 · CWC27 on Sugi Atlas →

0 patent compounds predicted against CWC27, 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 CWC27 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100 PHASE1/PHASE2COMPLETED
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Esophageal Cancer PHASE1COMPLETED
Study of Oral CNF2024 (BIIB021) in Advanced Solid Tumors PHASE1COMPLETED
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Gastric Cancer PHASE1COMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
PCD New Gene Discovery nanCOMPLETED
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Patient's Derived Organoids for Drug Screening in Glioblastoma nanNOT_YET_RECRUITING
Molecular Disease Profile of Hematological Malignancies nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Genome Sequencing in the Intensive Care Unit Population nanENROLLING_BY_INVITATION
Study of Constitutional Platelet Disease nanUNKNOWN
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Evaluation of Brain Dysfunction in Patients with Duchene Muscular Dystrophy nanNOT_YET_RECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Next Generation Sequencing of Normal Tissues Prospectively in Pediatric Oncology Patients nanRECRUITING
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a CWC27 binder may also engage these)

ProteinNameSimilarity
Q4R713 1.000 Q4R713 →
Q5R7W3 1.000 Q5R7W3 →
Q17QX9 1.000 Q17QX9 →
Q3TKY6 1.000 Q3TKY6 →
Q5XIB2 1.000 Q5XIB2 →
Q6GLX7 1.000 Q6GLX7 →
Q7ZW86 0.997 Q7ZW86 →
P0C1J2 0.997 P0C1J2 →
Q7SBX8 0.997 Q7SBX8 →
Q6Q152 0.997 Q6Q152 →
P0CP93 0.997 P0CP93 →
P0CP92 0.995 P0CP92 →
O42941 0.994 O42941 →
Q4IPB3 0.992 Q4IPB3 →
Q568K9 0.990 Q568K9 →
P0CR14 0.990 P0CR14 →
Q02770 0.990 Q02770 →
Q6CGK4 0.989 Q6CGK4 →
Q5AXT6 0.989 Q5AXT6 →
Q8H110 0.989 Q8H110 →
Q4IBK5 0.989 Q4IBK5 →
O13475 0.988 O13475 →
Q6BWH6 0.988 Q6BWH6 →
A5E3K3 0.988 A5E3K3 →
Q9WV03 0.988 Q9WV03 →
P34648 0.987 P34648 →
Q9FJX0 0.987 Q9FJX0 →
P38326 0.987 P38326 →
Q6FVX3 0.987 Q6FVX3 →
SMARCC2 SWI/SNF complex subunit SMARCC2 0.987 landscape →