YIF1A

Protein YIF1A · O95070 · YIF1A on Sugi Atlas →

0 patent compounds predicted against YIF1A, 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 YIF1A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Management of Retinitis Pigmentosa Via Combination of Wharton's Jelly-derived Mesenchymal Stem Cells and Magnovision PHASE3COMPLETED
NEO100 and High-Grade Meningioma PHASE2RECRUITING
Safety and Pharmacology of SNX-5422 Plus Carboplatin and Paclitaxel in Subjects With Solid Tumors PHASE1COMPLETED
Dynamics of Muscle Mitochondria in Type 2 Diabetes (DYNAMMO T2D) EARLY_PHASE1COMPLETED
Proteomics and Orthodontic Root Resorption nanCOMPLETED
X-chromosome Inactivation, Epigenetics and the Transcriptome nanCOMPLETED
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Role of KATP Channel Loss in Type 2 Diabetes nanRECRUITING
Measuring Protein Turnover in Humans Across the Lifespan by Metabolic Labeling With Deuterium Oxide nanRECRUITING
Genetic Causes of Male Infertility nanCOMPLETED
Dynamics of Muscle Mitochondria in Type 2 Diabetes Exercise nanCOMPLETED
X-Chromosome Inactivation Status and Premature Ovarian Failure nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Diagnosis and Phenotype Characterisation Using Genomics in Patients With Inherited Bone Marrow Failure (IBMDx Study) nanRECRUITING
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
Abnormalities in the Effects of Insulin and Exercise on Glucose- and Lipid Metabolism in Obesity and Type 2 Diabetes nanCOMPLETED
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Impact of Mutations in Aminoacyl tRNA Synthetases on Protein Translation and Cellular Stress nanWITHDRAWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Endolymphatic Sac Tumors in a Population of Patients With Von Hippel-Lindau Disease:The Natural History and Pathobiology, and a Prospective Non-Randomized Clinical Trial of Hearing Preservation Surgery in Patients With Early Stage Endolymphatic Sac Tumors nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Role of Amino Acids and Genetic Disorder in Pathogenesis of Heart Failure nanUNKNOWN
Effect of Branched Chain Amino Acids on Muscle nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a YIF1A binder may also engage these)

ProteinNameSimilarity
Q91XB7 1.000 Q91XB7 →
Q3T196 1.000 Q3T196 →
Q6P301 0.995 Q6P301 →
Q4FZQ0 0.995 Q4FZQ0 →
Q5U3G6 0.994 Q5U3G6 →
Q9CX30 0.994 Q9CX30 →
Q5BJH7 0.994 Q5BJH7 →
Q6PC24 0.994 Q6PC24 →
Q6GN58 0.993 Q6GN58 →
P87148 0.992 P87148 →
O94348 0.983 O94348 →
Q9BWQ6 0.981 Q9BWQ6 →
Q6P6G5 0.981 Q6P6G5 →
Q75IC7 0.981 Q75IC7 →
Q6PEC3 0.980 Q6PEC3 →
Q28FG4 0.979 Q28FG4 →
Q9UTD3 0.979 Q9UTD3 →
Q10045 0.978 Q10045 →
A2XX57 0.978 A2XX57 →
Q5RBL0 0.978 Q5RBL0 →
Q9Y548 0.978 Q9Y548 →
Q4W9R7 0.977 Q4W9R7 →
Q9UI14 0.977 Q9UI14 →
B0D4E6 0.977 B0D4E6 →
P53039 0.977 P53039 →
Q0DC45 0.977 Q0DC45 →
Q6GMB1 0.976 Q6GMB1 →
Q99LP8 0.976 Q99LP8 →
Q751P7 0.976 Q751P7 →
O49873 0.976 O49873 →