Sugi Predict

Sugi Predict / Targets / UNC119

UNC119

Protein unc-119 homolog A · Q13432 · UNC119 on Sugi Atlas →

0 patent compounds predicted against UNC119, 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 UNC119 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men PHASE3ACTIVE_NOT_RECRUITING
Histocompatibility Leukocyte Antigen (HLA)-A*0201 Restricted Peptide Vaccine Therapy in Patients With Esophageal Cancer PHASE1/PHASE2COMPLETED
Discovery and Validation of Genetic Variants Affecting Microglial Activation in Alzheimer's Disease PHASE2ACTIVE_NOT_RECRUITING
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Determinants and Clinical Consequences of Early-onset Severe Obesity nanUNKNOWN
Autophagy Bladder Cancer nanUNKNOWN
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Inherited Reproductive Disorders nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
C1q/TNF-related Protein 9 (CTRP 9) Level in Preeclamptic Obese and Non-obese Pregnancies nanCOMPLETED
Identification Genetic, Immunologic and Microbial Markers of Hirschsprung Associated Enterocolitis in Children With Hirschsprung Disease nanUNKNOWN
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
The Canadian Multicentre CSF Monitoring and Biomarker Study nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Stakeholders of Rare Diseases Informing Values In Neuroethics nanRECRUITING
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study nanUNKNOWN
Natural History of Photoreceptor Degeneration in USH1B: Clinical Parameters and Validation of Functional Vision Tests in MYO7A nanRECRUITING
Pathophysiology of Diabetic Gastroparesis nanUNKNOWN
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Congenital Hemolytic and Dyserythropoietic Anemias nanRECRUITING
Study of Constitutional Platelet Disease nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Familial Intracranial Aneurysm Study II nanCOMPLETED
Defining the Brain Phenotype of Children With Williams Syndrome nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a UNC119 binder may also engage these)

ProteinNameSimilarity
Q3SYR2 — 1.000 Q3SYR2 →
Q66JA9 — 1.000 Q66JA9 →
Q6INE2 — 1.000 Q6INE2 →
O19177 — 0.999 O19177 →
Q9Z2R6 — 0.998 Q9Z2R6 →
Q90Z08 — 0.996 Q90Z08 →
Q62885 — 0.996 Q62885 →
A6NIH7 — 0.995 A6NIH7 →
Q8C4B4 — 0.992 Q8C4B4 →
B4Q785 — 0.991 B4Q785 →
Q9XYQ2 — 0.991 Q9XYQ2 →
Q9NA64 — 0.991 Q9NA64 →
B4HYQ2 — 0.991 B4HYQ2 →
Q9D771 — 0.991 Q9D771 →
Q03345 — 0.990 Q03345 →
Q17QJ0 — 0.990 Q17QJ0 →
Q10658 — 0.990 Q10658 →
P55082 — 0.990 P55082 →
Q9VLJ0 — 0.990 Q9VLJ0 →
B4NXG9 — 0.990 B4NXG9 →
PDE6D Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta 0.990 landscape →
Q0V9Z3 — 0.990 Q0V9Z3 →
P36318 — 0.989 P36318 →
Q9NVP2 — 0.989 Q9NVP2 →
P06476 — 0.989 P06476 →
P54634 — 0.989 P54634 →
Q2YDM0 — 0.989 Q2YDM0 →
A1Z0Q5 — 0.989 A1Z0Q5 →
P24872 — 0.989 P24872 →
C5DMZ6 — 0.988 C5DMZ6 →