SNX9

Sorting nexin-9 · Q9Y5X1 · SNX9 on Sugi Atlas →

0 patent compounds predicted against SNX9, 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 SNX9 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Mitochondrial Membrane Protein Neurodegeneration (MPAN) nanCOMPLETED
Natural History Study of GEMIN-5 Related Neurodevelopmental Disorder nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Chromosome 9 P Minus Syndrome nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Studying Chromosomes in Samples From Younger Patients With Neuroblastoma nanCOMPLETED
Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing nanCOMPLETED
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C nanRECRUITING
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
DDX3X Syndrome -The Seaver Autism Center for Research and Treatment is Characterizing DDX3X-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures. nanCOMPLETED
Screening for Genes in Patients With Congenital Neutropenia nanCOMPLETED
Better Delineation of YY1 Related Phenotype and Epigenetic Signatures. nanUNKNOWN
Implementation of Molecular Diagnostic Pathways nanUNKNOWN
Longitudinal Study of Neurogenetic Disorders nanRECRUITING
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
The Role of DNA and RNA in NGS Analyses for Advaced Stage NSCLC Patients nanRECRUITING
Mackenzie's Mission: The Australian Reproductive Carrier Screening Project nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SNX9 binder may also engage these)

ProteinNameSimilarity
Q91VH2 1.000 Q91VH2 →
Q5R9A9 0.987 Q5R9A9 →
P0C220 0.984 P0C220 →
Q9CWK8 0.983 Q9CWK8 →
SNX2 Sorting nexin-2 0.982 landscape →
Q0JRZ9 0.981 Q0JRZ9 →
Q9UHR4 0.981 Q9UHR4 →
Q2TBW7 0.981 Q2TBW7 →
Q5R807 0.981 Q5R807 →
Q3KR97 0.980 Q3KR97 →
Q9DBJ3 0.980 Q9DBJ3 →
Q8I4E2 0.980 Q8I4E2 →
PACSIN2 Protein kinase C and casein kinase substrate in neurons protein 2 0.980 landscape →
SNX1 Sorting nexin-1 0.978 landscape →
Q2UB56 0.978 Q2UB56 →
A2APV2 0.978 A2APV2 →
Q3UQN2 0.978 Q3UQN2 →
Q07139 0.978 Q07139 →
Q99N27 0.977 Q99N27 →
Q9BXB4 0.977 Q9BXB4 →
Q5R411 0.977 Q5R411 →
DNAJC13 DnaJ homolog subfamily C member 13 0.977 landscape →
Q80TJ1 0.977 Q80TJ1 →
Q9H8V3 0.977 Q9H8V3 →
D3ZYR1 0.977 D3ZYR1 →
Q5RFP8 0.977 Q5RFP8 →
PTK2 Focal adhesion kinase 1 0.976 landscape →
Q5ZJJ5 0.976 Q5ZJJ5 →
Q9QY17 0.976 Q9QY17 →
Q86UW7 0.976 Q86UW7 →