THOC2

THO complex subunit 2 · Q8NI27 · THOC2 on Sugi Atlas →

0 patent compounds predicted against THOC2, 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 THOC2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
MEHMO Natural History and Biomarkers nanRECRUITING
Hearts in Rhythm Organization (HiRO)National Registry and Bio Bank nanENROLLING_BY_INVITATION
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Monogenic Diabetes Misdiagnosed as Type 1 nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs) nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Family Blood Pressure Program - GENOA nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
A Study on Risk Mutations of Vulnerability Genes of Schizophrenia nanUNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Mechanisms and Additional Risk Factors Underlying Hip Dysplasia nanCOMPLETED
Genes Modulating the Severity of Aortic Aneurysms (MSF1-TGFBR2) nanUNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Gut Microbiome in Patients With Polycystic Ovary Syndrome nanUNKNOWN
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a THOC2 binder may also engage these)

ProteinNameSimilarity
B1MTK1 1.000 B1MTK1 →
B0KWH8 1.000 B0KWH8 →
B2KI97 1.000 B2KI97 →
C1FXW9 1.000 C1FXW9 →
B1AZI6 1.000 B1AZI6 →
Q6GQD0 0.985 Q6GQD0 →
Q7TPD0 0.984 Q7TPD0 →
C0H906 0.983 C0H906 →
Q6GQ80 0.982 Q6GQ80 →
Q5ZJZ6 0.980 Q5ZJZ6 →
Q56A27 0.980 Q56A27 →
NCBP1 Nuclear cap-binding protein subunit 1 0.979 landscape →
Q8BWQ6 0.978 Q8BWQ6 →
Q5RE70 0.978 Q5RE70 →
Q8IWV8 0.976 Q8IWV8 →
Q6WKZ8 0.976 Q6WKZ8 →
A2AT37 0.975 A2AT37 →
Q6DIE2 0.975 Q6DIE2 →
Q4R6R4 0.975 Q4R6R4 →
Q6PAL8 0.974 Q6PAL8 →
Q3UYV9 0.974 Q3UYV9 →
Q68E01 0.974 Q68E01 →
Q9HAU5 0.974 Q9HAU5 →
A4VCH4 0.974 A4VCH4 →
Q803T2 0.973 Q803T2 →
Q6PD83 0.972 Q6PD83 →
Q6QI06 0.972 Q6QI06 →
O00507 0.972 O00507 →
Q8C8N2 0.972 Q8C8N2 →
Q9WTT7 0.972 Q9WTT7 →