TXNDC17

Thioredoxin domain-containing protein 17 · Q9BRA2 · TXNDC17 on Sugi Atlas →

0 patent compounds predicted against TXNDC17, 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 TXNDC17 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Testing the Combination of MLN4924 (Pevonedistat), Carboplatin, and Paclitaxel in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) Who Have Previously Been Treated With Immunotherapy PHASE2ACTIVE_NOT_RECRUITING
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Esophageal Cancer PHASE1COMPLETED
Tolerability of Enteral NAC in Infants PHASE1NOT_YET_RECRUITING
S9304A Study of Protein Expression in Tumor Tissue Samples From Patients With Stage II or Stage III Rectal Cancer Enrolled in Clinical Trial SWOG-9304 nanCOMPLETED
Serum Betatrophin Levels and Its Influencing Factors in Patients With Hyperthyroidism nanUNKNOWN
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Genetic Variation in TRAF3IP2 (rs13190932) nanRECRUITING
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Cause of Familial Testicular Cancer nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Abnormalities in the Effects of Insulin and Exercise on Glucose- and Lipid Metabolism in Obesity and Type 2 Diabetes nanCOMPLETED
Molecular & Clinical Evaluation of Low HDL Syndromes nanCOMPLETED
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Telomere Disclosure and Impact on Psychological Distress and Health Behaviors nanCOMPLETED
NCF Gene & TNFSF4 in SLE Patients nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Genetics of Familial Testicular Cancer nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Measuring Protein Turnover in Humans Across the Lifespan by Metabolic Labeling With Deuterium Oxide nanRECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Identification of Diabetic Nephropathy Biomarkers Through Transcriptomics nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a TXNDC17 binder may also engage these)

ProteinNameSimilarity
Q5REA8 1.000 Q5REA8 →
Q5NVN7 0.935 Q5NVN7 →
SAE1 SUMO-activating enzyme subunit 1 0.932 landscape →
A2VE14 0.929 A2VE14 →
Q6AXQ0 0.927 Q6AXQ0 →
P51583 0.926 P51583 →
Q9DCL9 0.925 Q9DCL9 →
PAICS Bifunctional phosphoribosylaminoimidazole carboxylase/phosphoribosylaminoimidazole succinocarboxamide synthetase 0.924 landscape →
Q5RB59 0.923 Q5RB59 →
Q8BGB7 0.921 Q8BGB7 →
Q9R1T2 0.919 Q9R1T2 →
Q9JIB4 0.918 Q9JIB4 →
HDAC8 Histone deacetylase 8 0.918 landscape →
P38024 0.918 P38024 →
B1WC68 0.916 B1WC68 →
Q0VCB2 0.915 Q0VCB2 →
Q9UHY7 0.915 Q9UHY7 →
A0JN27 0.915 A0JN27 →
O89050 0.914 O89050 →
Q6NRQ7 0.914 Q6NRQ7 →
Q58CY6 0.914 Q58CY6 →
Q5JPE7 0.914 Q5JPE7 →
Q67FW5 0.914 Q67FW5 →
Q5RB35 0.914 Q5RB35 →
Q9UL63 0.913 Q9UL63 →
Q0VD27 0.913 Q0VD27 →
D3ZVR7 0.913 D3ZVR7 →
Q86XW9 0.912 Q86XW9 →
P20595 0.912 P20595 →
Q8BUH1 0.912 Q8BUH1 →