Sugi Predict

Sugi Predict / Targets / TBL1XR1

TBL1XR1

F-box-like/WD repeat-containing protein TBL1XR1 · Q9BZK7 · TBL1XR1 on Sugi Atlas →

0 patent compounds predicted against TBL1XR1, 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 TBL1XR1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Evaluation of a Cancer Lysate Vaccine and Montanide (Registered Trademark) ISA-51 VG With or Without the IL-15 Super-Agonist N-803 as Adjuvant Therapy for PD-L1 Negative Non-Small Cell Lung Cancer PHASE1/PHASE2SUSPENDED
Efficacy and Safety Assessment of Oral LBH589 in Adult Patients With Advanced Soft TIssue Sarcoma After Pre-treatment Failure PHASE2COMPLETED
Genetic Clues to Chordoma Etiology: A Protocol to Identify Sporadic Chordoma Patients for Studies of Cancer-Susceptibility Genes nanACTIVE_NOT_RECRUITING
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Natural History of Acquired and Inherited Bone Marrow Failure Syndromes nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
The Role of TBX3 in Human ES Cell Differentiation nanWITHDRAWN
Clinical and Genetic Studies of VACTERL Association nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Linkage Study in Familial Pulmonary Fibrosis nanCOMPLETED
Elucidating the Genetic Basis of the Pleuropulmonary Blastoma (PPB) Familial Cancer Syndrome nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Autophagy Bladder Cancer nanUNKNOWN
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
UTHealth Turner Syndrome Research Registry nanRECRUITING
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Biology of Thymic Tumors nanCOMPLETED
Amplification of Zinc Finger Protein 217 Gene in Multiple Myeloma nanUNKNOWN
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a TBL1XR1 binder may also engage these)

ProteinNameSimilarity
Q8BHJ5 — 1.000 Q8BHJ5 →
Q6GPC6 — 1.000 Q6GPC6 →
Q7SZM9 — 1.000 Q7SZM9 →
Q9QXE7 — 1.000 Q9QXE7 →
Q9BQ87 — 0.993 Q9BQ87 →
Q4R8H1 — 0.982 Q4R8H1 →
O60907 — 0.981 O60907 →
Q8R2U0 — 0.969 Q8R2U0 →
Q5RAN6 — 0.968 Q5RAN6 →
Q96EE3 — 0.967 Q96EE3 →
A7YY75 — 0.961 A7YY75 →
Q4FZW5 — 0.959 Q4FZW5 →
Q9V3J8 — 0.954 Q9V3J8 →
Q6GNF1 — 0.953 Q6GNF1 →
Q5U4Y8 — 0.953 Q5U4Y8 →
Q92747 — 0.947 Q92747 →
DHX9 ATP-dependent RNA helicase A 0.945 landscape →
Q9R0Q6 — 0.944 Q9R0Q6 →
Q1JP79 — 0.944 Q1JP79 →
Q99LC2 — 0.944 Q99LC2 →
Q5R8K2 — 0.944 Q5R8K2 →
Q5BJQ6 — 0.944 Q5BJQ6 →
Q99PD4 — 0.943 Q99PD4 →
Q5R874 — 0.941 Q5R874 →
Q640J6 — 0.939 Q640J6 →
P17427 — 0.939 P17427 →
Q8BFQ4 — 0.938 Q8BFQ4 →
P18484 — 0.938 P18484 →
WDR82 WD repeat-containing protein 82 0.938 landscape →
Q6GL39 — 0.938 Q6GL39 →