TFIP11

Tuftelin-interacting protein 11 · Q9UBB9 · TFIP11 on Sugi Atlas →

0 patent compounds predicted against TFIP11, 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 TFIP11 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study on the Tolerability and Early Efficacy of hLF1-11 in Patients With Proven Candidaemia PHASE1/PHASE2WITHDRAWN
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Esophageal Cancer PHASE1COMPLETED
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Gastric Cancer PHASE1COMPLETED
Combination of Chemoradiation Therapy and Epitope Peptide Vaccine Therapy in Treating Patients With Esophageal Cancer PHASE1UNKNOWN
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Better Delineation of BCL11B Related Phenotype and Epigenetic Signature. nanCOMPLETED
VDR and TFIP11 Gene Polymorphism and Gene-environmental Interaction in Adults nanCOMPLETED
Implication of Genetic Variations in Long Intergenic Non-coding RNA 00511 (LINC00511) in Colorectal Cancer nanCOMPLETED
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Amplification of Zinc Finger Protein 217 Gene in Multiple Myeloma nanUNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease. nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies nanCOMPLETED
Genetic Basis of Mitral Valve Prolapse nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Susceptibility to Infections in Ataxia Telangiectasia nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a TFIP11 binder may also engage these)

ProteinNameSimilarity
A1XD94 1.000 A1XD94 →
Q5R5K8 1.000 Q5R5K8 →
A1XD95 1.000 A1XD95 →
A1XD93 1.000 A1XD93 →
Q5U2Y6 1.000 Q5U2Y6 →
A1XD97 1.000 A1XD97 →
A4UMC6 1.000 A4UMC6 →
Q29RR5 1.000 Q29RR5 →
Q5ZII9 1.000 Q5ZII9 →
Q66J74 1.000 Q66J74 →
Q0IIX9 1.000 Q0IIX9 →
Q9ERA6 1.000 Q9ERA6 →
Q9SHG6 1.000 Q9SHG6 →
A4UMC5 1.000 A4UMC5 →
Q06AK6 1.000 Q06AK6 →
Q9Y103 1.000 Q9Y103 →
Q6DI35 1.000 Q6DI35 →
Q9SLC6 0.998 Q9SLC6 →
O54774 0.992 O54774 →
A7SBN6 0.991 A7SBN6 →
Q9FG01 0.990 Q9FG01 →
Q28653 0.990 Q28653 →
Q17784 0.990 Q17784 →
PPP2R5D Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform 0.990 landscape →
Q58CP9 0.990 Q58CP9 →
Q2KI89 0.990 Q2KI89 →
Q32NW2 0.990 Q32NW2 →
Q9UTK6 0.990 Q9UTK6 →
Q86T65 0.990 Q86T65 →
Q7Z3E5 0.989 Q7Z3E5 →