Sugi Predict

Sugi Predict / Targets / SNX3

SNX3

Sorting nexin-3 · O60493 · SNX3 on Sugi Atlas →

0 patent compounds predicted against SNX3, 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 SNX3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Hydroxychloroquin (HCQ) in chILD of Genetic Defect nanCOMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Implementation of Molecular Diagnostic Pathways nanUNKNOWN
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
The Roles of Neutrophil Elastase in Lung Cancer nanUNKNOWN
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SNX3 binder may also engage these)

ProteinNameSimilarity
Q5U211 — 1.000 Q5U211 →
Q1RMH8 — 1.000 Q1RMH8 →
Q5R5V1 — 1.000 Q5R5V1 →
O70492 — 0.999 O70492 →
O70493 — 0.980 O70493 →
Q6C2S9 — 0.955 Q6C2S9 →
Q4I1H6 — 0.938 Q4I1H6 →
Q9UMY4 — 0.937 Q9UMY4 →
P0CR61 — 0.932 P0CR61 →
Q4WWS3 — 0.919 Q4WWS3 →
Q2U4K2 — 0.919 Q2U4K2 →
Q66HR2 — 0.909 Q66HR2 →
P48455 — 0.908 P48455 →
P48454 — 0.908 P48454 →
Q3ZBD9 — 0.907 Q3ZBD9 →
Q5R7Z5 — 0.907 Q5R7Z5 →
Q61166 — 0.907 Q61166 →
Q5ZKU1 — 0.907 Q5ZKU1 →
MAPRE1 Microtubule-associated protein RP/EB family member 1 0.905 landscape →
Q9VXF1 — 0.905 Q9VXF1 →
Q27889 — 0.905 Q27889 →
DCUN1D1 DCN1-like protein 1 0.904 landscape →
Q5ZLC7 — 0.904 Q5ZLC7 →
Q0G819 — 0.903 Q0G819 →
Q9QZ73 — 0.903 Q9QZ73 →
Q9M2R0 — 0.903 Q9M2R0 →
Q66T82 — 0.903 Q66T82 →
Q6V291 — 0.902 Q6V291 →
Q1RMS5 — 0.902 Q1RMS5 →
YEATS4 YEATS domain-containing protein 4 0.901 landscape →