Sugi Predict

Sugi Predict / Targets / TBC1D5

TBC1D5

TBC1 domain family member 5 · Q92609 · TBC1D5 on Sugi Atlas →

0 patent compounds predicted against TBC1D5, 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 TBC1D5 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Danazol for Genetic Bone Marrow and Lung Disorders PHASE1/PHASE2COMPLETED
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
Phenotypic and Genotypic Characterization of Patients With Dysmetabolism in Greenland nanRECRUITING
Natural History of Acquired and Inherited Bone Marrow Failure Syndromes nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches. nanRECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
The Genetics of Cardiomyopathy and Heart Failure nanWITHDRAWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Role of Polymorphisms in the IL-1 Gene Cluster nanCOMPLETED
Mayo AVC Registry and Biobank nanRECRUITING
Genetics of Cardiovascular and Neuromuscular Disease nanRECRUITING
Idiopathic Dilated Cardiomyopathy nanCOMPLETED
Rab 32 Gene Polymorphisms as a Prognostic Factor in Leprosy Patients nanRECRUITING
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
UTHealth Turner Syndrome Research Registry nanRECRUITING
Outcome of Different Pathogenic Mutations in Hypertrophic Cardiomyopathy nanUNKNOWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Correlation Between Myocardial Deformation and Coronary Artery Tortuosity in Patients With Hypertrophic Cardiomyopathy nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Dilated Cardiomyopathy-Cardiac Magnetic Resonance (DCM-CMR) Ancillary Study nanACTIVE_NOT_RECRUITING
South Asian Arrhythmogenic Cardiomyopathy Registry nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a TBC1D5 binder may also engage these)

ProteinNameSimilarity
Q80XQ2 — 1.000 Q80XQ2 →
Q9URY3 — 0.993 Q9URY3 →
O43078 — 0.991 O43078 →
I2HAA0 — 0.991 I2HAA0 →
B4NBP4 — 0.991 B4NBP4 →
A8XQD5 — 0.990 A8XQD5 →
P41846 — 0.990 P41846 →
B3M301 — 0.990 B3M301 →
P43125 — 0.990 P43125 →
P34489 — 0.990 P34489 →
Q6ZPS6 — 0.989 Q6ZPS6 →
O43166 — 0.989 O43166 →
A8E7C5 — 0.989 A8E7C5 →
Q6E3D4 — 0.989 Q6E3D4 →
Q84T61 — 0.989 Q84T61 →
Q08639 — 0.989 Q08639 →
Q95RG8 — 0.989 Q95RG8 →
Q1LYM3 — 0.989 Q1LYM3 →
DHX29 ATP-dependent RNA helicase DHX29 0.989 landscape →
B3H615 — 0.989 B3H615 →
G5EFI8 — 0.989 G5EFI8 →
Q08AX9 — 0.989 Q08AX9 →
Q756C4 — 0.989 Q756C4 →
P61406 — 0.989 P61406 →
Q5JCS6 — 0.989 Q5JCS6 →
P48479 — 0.989 P48479 →
P43638 — 0.989 P43638 →
Q9Y2H2 — 0.989 Q9Y2H2 →
Q74ZH7 — 0.988 Q74ZH7 →
Q2NKQ1 — 0.988 Q2NKQ1 →