Sugi Predict

Sugi Predict / Targets / SNX2

SNX2

Sorting nexin-2 · O60749 · SNX2 on Sugi Atlas →

0 patent compounds predicted against SNX2, 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 SNX2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing nanCOMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
The Roles of Neutrophil Elastase in Lung Cancer nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Cardiovascular Effects of Empagliflozine nanUNKNOWN
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
North Carolina Genomic Evaluation by Next-generation Exome Sequencing, 2 nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Longitudinal Study of Cognition With Niemann-Pick Disease, Type C nanCOMPLETED
Mackenzie's Mission: The Australian Reproductive Carrier Screening Project nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Genetics of Neonatal Encephalopathy and Related Disorders nanRECRUITING
Hereditary Tubulointerstitial Nephritis nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a SNX2 binder may also engage these)

ProteinNameSimilarity
Q5R9A9 — 1.000 Q5R9A9 →
Q9CWK8 — 1.000 Q9CWK8 →
P0C220 — 1.000 P0C220 →
Q2TBW7 — 1.000 Q2TBW7 →
SNX1 Sorting nexin-1 0.991 landscape →
Q99N27 — 0.989 Q99N27 →
Q5RFP8 — 0.989 Q5RFP8 →
Q05B62 — 0.988 Q05B62 →
Q4R503 — 0.987 Q4R503 →
B9DFS6 — 0.984 B9DFS6 →
Q9WV80 — 0.983 Q9WV80 →
Q8L5Z7 — 0.981 Q8L5Z7 →
SNX9 Sorting nexin-9 0.979 landscape →
Q0JRZ9 — 0.978 Q0JRZ9 →
Q5R807 — 0.978 Q5R807 →
Q9UHR4 — 0.976 Q9UHR4 →
Q3UQN2 — 0.975 Q3UQN2 →
D3ZYR1 — 0.974 D3ZYR1 →
Q9DBJ3 — 0.974 Q9DBJ3 →
Q0WQF4 — 0.974 Q0WQF4 →
Q3KR97 — 0.974 Q3KR97 →
Q91VH2 — 0.974 Q91VH2 →
Q9BXB4 — 0.972 Q9BXB4 →
Q9QY17 — 0.971 Q9QY17 →
Q8L7W0 — 0.971 Q8L7W0 →
Q9DDA9 — 0.971 Q9DDA9 →
A2APV2 — 0.971 A2APV2 →
Q5M7Y0 — 0.971 Q5M7Y0 →
PACSIN2 Protein kinase C and casein kinase substrate in neurons protein 2 0.970 landscape →
Q8CI95 — 0.970 Q8CI95 →