SNX1

Sorting nexin-1 · Q13596 · SNX1 on Sugi Atlas →

0 patent compounds predicted against SNX1, 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 SNX1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Nilotinib in Huntington's Disease PHASE1UNKNOWN
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
Studying Chromosomes in Samples From Younger Patients With Neuroblastoma nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetics of Neonatal Encephalopathy and Related Disorders nanRECRUITING
Baker Gordon Syndrome Natural History Study nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing nanUNKNOWN
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
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
Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing 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
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SNX1 binder may also engage these)

ProteinNameSimilarity
Q5RFP8 1.000 Q5RFP8 →
Q05B62 1.000 Q05B62 →
Q4R503 1.000 Q4R503 →
Q99N27 1.000 Q99N27 →
Q9WV80 1.000 Q9WV80 →
Q5R9A9 0.995 Q5R9A9 →
P0C220 0.993 P0C220 →
Q9CWK8 0.992 Q9CWK8 →
Q2TBW7 0.991 Q2TBW7 →
SNX2 Sorting nexin-2 0.990 landscape →
B9DFS6 0.986 B9DFS6 →
Q8CJ53 0.983 Q8CJ53 →
Q8L5Z7 0.983 Q8L5Z7 →
Q5RCJ1 0.982 Q5RCJ1 →
Q52LW3 0.981 Q52LW3 →
Q8CI04 0.981 Q8CI04 →
O08839 0.981 O08839 →
Q9FG38 0.981 Q9FG38 →
O35180 0.981 O35180 →
Q5PQJ5 0.981 Q5PQJ5 →
Q8WV41 0.980 Q8WV41 →
Q15642 0.980 Q15642 →
O08539 0.980 O08539 →
O94868 0.980 O94868 →
Q8R3V5 0.980 Q8R3V5 →
Q3USJ8 0.980 Q3USJ8 →
Q8NDH6 0.980 Q8NDH6 →
O00499 0.980 O00499 →
Q923U0 0.980 Q923U0 →
Q5ZJ81 0.980 Q5ZJ81 →