SNW1

SNW domain-containing protein 1 · Q13573 · SNW1 on Sugi Atlas →

0 patent compounds predicted against SNW1, 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 SNW1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment With HMG-COA Reductase Inhibitor of Growth and Bone Abnormalities in Children With Noonan Syndrome PHASE3COMPLETED
Scleral Buckling for Retinal Detachment Prevention in Genetically Confirmed Stickler Syndrome PHASE2WITHDRAWN
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
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 Blood Samples From High-Risk Postmenopausal Women Who Received Treatment on Breast Cancer Prevention Clinical Trials NSABP-P-1 or NSABP-P-2 nanUNKNOWN
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
The Phenotyping and Genotyping of Taiwanese Patients With Obstructive Sleep Apnea nanUNKNOWN
Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Screening for Genes in Patients With Congenital Neutropenia nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Establishment of Genomic and Phenotypic Database for Niemann-Pick Disease, Type C nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Emerging Role of NOTCH-related Long Non-coding RNA(s) as Biomarkers in Liquid Biopsy From Colorectal Cancer Patients nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Genetic Identification (ID) of Segmental Dysplastic Nevi nanWITHDRAWN
Better Delineation of YY1 Related Phenotype and Epigenetic Signatures. nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Study of Individuals and Families With Aberrations in DDX41 or Similar Cancer Predisposition Variants nanRECRUITING
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
iPSC Neurons From Adult Survivors of Childhood Cancer Who Have Persistent Vincristine-Induced Neuropathy nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a SNW1 binder may also engage these)

ProteinNameSimilarity
Q9CSN1 1.000 Q9CSN1 →
Q1JQE0 1.000 Q1JQE0 →
Q5R7R9 1.000 Q5R7R9 →
Q6K8D9 1.000 Q6K8D9 →
P0CR57 1.000 P0CR57 →
P39736 1.000 P39736 →
Q09882 1.000 Q09882 →
Q4PB95 1.000 Q4PB95 →
P28004 1.000 P28004 →
Q4WEH7 1.000 Q4WEH7 →
Q5AU50 1.000 Q5AU50 →
O80653 0.999 O80653 →
Q22836 0.999 Q22836 →
P0CR56 0.999 P0CR56 →
Q6CC77 0.998 Q6CC77 →
Q6CLJ7 0.996 Q6CLJ7 →
Q8GWI5 0.995 Q8GWI5 →
Q9LFE0 0.994 Q9LFE0 →
Q759B6 0.994 Q759B6 →
Q6FIT9 0.994 Q6FIT9 →
Q753K4 0.993 Q753K4 →
Q9VR99 0.992 Q9VR99 →
P0CR52 0.992 P0CR52 →
Q8WZL6 0.991 Q8WZL6 →
Q9Y7Z6 0.991 Q9Y7Z6 →
P0CO17 0.991 P0CO17 →
Q75E62 0.991 Q75E62 →
B7UNI8 0.991 B7UNI8 →
Q9P7S9 0.991 Q9P7S9 →
Q6FRY5 0.991 Q6FRY5 →