TBC1D15

TBC1 domain family member 15 · Q8TC07 · TBC1D15 on Sugi Atlas →

0 patent compounds predicted against TBC1D15, 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 TBC1D15 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Danazol for Genetic Bone Marrow and Lung Disorders PHASE1/PHASE2COMPLETED
Phase 1 Study Of TROP2 CAR/IL-15 TGFBR2 KO NK Cell In Patients With Oral Premalignant Lesions PHASE1NOT_YET_RECRUITING
The Role of TBC1D4 in Exercise- and Insulin-induced Glucose Metabolism in Human Skeletal Muscle nanCOMPLETED
The Role of Traditional or Western Diet in the TBC1D4 Gene on Glucose Homeostasis in Greenland Inuits nanCOMPLETED
Natural History of Acquired and Inherited Bone Marrow Failure Syndromes nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Outcome of Different Pathogenic Mutations in Hypertrophic Cardiomyopathy nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Epileptic Syndromes in Infants and Early Childhood nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Role of Polymorphisms in the IL-1 Gene Cluster nanCOMPLETED
Idiopathic Dilated Cardiomyopathy nanCOMPLETED
Mayo AVC Registry and Biobank nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Tuberous Sclerosis Complex and Lymphangioleiomyomatosis Pregnancy Registry (TSC-LAM Registry) nanRECRUITING
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
UTHealth Turner Syndrome Research Registry nanRECRUITING
Clinical and Genetic Examinations of Dilated Cardiomyopathy nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches. nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a TBC1D15 binder may also engage these)

ProteinNameSimilarity
Q9CXF4 1.000 Q9CXF4 →
A6H8I2 0.990 A6H8I2 →
Q8VCZ6 0.989 Q8VCZ6 →
Q66K14 0.988 Q66K14 →
Q7T2D0 0.987 Q7T2D0 →
Q6ZT07 0.987 Q6ZT07 →
Q5SVR0 0.986 Q5SVR0 →
Q3UYK3 0.986 Q3UYK3 →
O97790 0.986 O97790 →
Q6P6R7 0.986 Q6P6R7 →
Q60949 0.985 Q60949 →
E9PUQ8 0.985 E9PUQ8 →
Q9BZF3 0.985 Q9BZF3 →
Q86TI0 0.985 Q86TI0 →
B0R0W9 0.984 B0R0W9 →
Q92503 0.984 Q92503 →
Q9Y4G8 0.984 Q9Y4G8 →
Q60695 0.984 Q60695 →
P70600 0.984 P70600 →
Q8CHG7 0.983 Q8CHG7 →
Q96HU1 0.983 Q96HU1 →
F1M386 0.983 F1M386 →
Q7Z3E5 0.983 Q7Z3E5 →
Q86YR7 0.983 Q86YR7 →
Q7Z401 0.983 Q7Z401 →
F1PBJ0 0.983 F1PBJ0 →
Q9NU19 0.983 Q9NU19 →
O95759 0.983 O95759 →
Q6AZT6 0.983 Q6AZT6 →
Q8R5A6 0.983 Q8R5A6 →