Sugi Predict

Sugi Predict / Targets / CLNS1A

CLNS1A

Methylosome subunit pICln · P54105 · CLNS1A on Sugi Atlas →

0 patent compounds predicted against CLNS1A, 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 CLNS1A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants. nanUNKNOWN
DNA Methylation and Perioperative Pain Treatment nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Novel Biomarkers in the Neoplastic Progression of Barrett's Esophagus nanACTIVE_NOT_RECRUITING
Emotional Regulation in Children With ND: the Role of Genomic Variation, Proteomic Patterns, and Early Experience nanUNKNOWN
Genetic Aspects of Neurologic and Psychiatric Disorders nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Identification of New FTLD Genes nanUNKNOWN
Effects of Epigenetic Regulation in Chronic Pelvic Pain Syndrome nanACTIVE_NOT_RECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Exploration and Verification of DNA Methylolation in Early Screening of Esophageal Cancer nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
The Etiology and Progression of Brain Tumors nanCOMPLETED
Genes, Proteins, and Metabolites in Drug-resistant Epilepsy (DRE) Patients nanNOT_YET_RECRUITING
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
The Genetic Characterization of Dementia nanCOMPLETED
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex nanCOMPLETED
Phenotype/Genotype Correlations in Neuromuscular Disorders nanCOMPLETED
Genomic Analysis of Families With a History of Discordant Cancers nanRECRUITING
Defining an Obesity QTL on Chromosome 3q nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genomics, Single Nucleotide Polymorphisms (SNPs), and Clinical Neonatology nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CLNS1A binder may also engage these)

ProteinNameSimilarity
Q61189 — 1.000 Q61189 →
Q28678 — 1.000 Q28678 →
Q04753 — 1.000 Q04753 →
Q5R719 — 1.000 Q5R719 →
P35521 — 0.994 P35521 →
P54106 — 0.987 P54106 →
Q9LVA7 — 0.987 Q9LVA7 →
Q9UNN5 — 0.963 Q9UNN5 →
Q9R1C0 — 0.962 Q9R1C0 →
CLTA Clathrin light chain A 0.962 landscape →
P54731 — 0.962 P54731 →
O48726 — 0.961 O48726 →
Q924K2 — 0.961 Q924K2 →
Q5XI81 — 0.961 Q5XI81 →
Q2HJG8 — 0.961 Q2HJG8 →
Q6DKA1 — 0.960 Q6DKA1 →
Q91WR3 — 0.960 Q91WR3 →
P55035 — 0.960 P55035 →
O35226 — 0.960 O35226 →
Q6DG43 — 0.960 Q6DG43 →
P32780 — 0.960 P32780 →
Q9XHM1 — 0.960 Q9XHM1 →
Q58A65 — 0.959 Q58A65 →
Q7ZYB4 — 0.959 Q7ZYB4 →
P70483 — 0.959 P70483 →
Q6R1L1 — 0.959 Q6R1L1 →
Q94JZ8 — 0.958 Q94JZ8 →
Q6PFL6 — 0.958 Q6PFL6 →
Q8LQ36 — 0.958 Q8LQ36 →
Q63945 — 0.958 Q63945 →