SND1

Staphylococcal nuclease domain-containing protein 1 · Q7KZF4 · SND1 on Sugi Atlas →

0 patent compounds predicted against SND1, 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 SND1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
A Phase I Trial of SHR3162 in Subjects With Advanced Solid Tumors PHASE1COMPLETED
Bortezomib Followed by Pembrolizumab and Cisplatin in metTNBC EARLY_PHASE1RECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Circulating Markers That Underlie the Transition From Compensated Hypertrophy to Heart Failure nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
SMYD3-Driven Metabolic Rewiring in Colorectal Liver Metastases nanNOT_YET_RECRUITING
Circulating Markers for Ischemic Heart Disease nanRECRUITING
Telomere Repair Gene Mutation in Inflammatory Bowel Disease nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Shwachman-Diamond Syndrome Global Patient Survey and Partnering Platform nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
High-Density Lipoprotein (HDL) Treatment Study nanCOMPLETED
Genetic Risk Factors of the Sneddon Syndrome nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
International PPB/DICER1 Registry nanRECRUITING
commd7 Gene Expression in ALL nanUNKNOWN
Genetics of Neonatal Encephalopathy and Related Disorders nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
DNA Damage & Repair Proteins In Patients With Atherosclerotic Coronary Artery Disease nanCOMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
Apoptosis Markers in Aggressive Periodontitis nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SND1 binder may also engage these)

ProteinNameSimilarity
Q66X93 1.000 Q66X93 →
Q863B3 1.000 Q863B3 →
Q78PY7 1.000 Q78PY7 →
Q5REU4 1.000 Q5REU4 →
Q7ZT42 0.999 Q7ZT42 →
CSDE1 Cold shock domain-containing protein E1 0.930 landscape →
P18395 0.928 P18395 →
Q91W50 0.927 Q91W50 →
Q6NXG1 0.920 Q6NXG1 →
Q2RAK2 0.918 Q2RAK2 →
Q8TCS8 0.917 Q8TCS8 →
Q3US41 0.916 Q3US41 →
Q9HBG6 0.916 Q9HBG6 →
Q5XGS8 0.916 Q5XGS8 →
Q52KW8 0.916 Q52KW8 →
Q4R4I8 0.916 Q4R4I8 →
Q5R8Q7 0.915 Q5R8Q7 →
Q3UGF1 0.915 Q3UGF1 →
Q863I2 0.915 Q863I2 →
F1QGH9 0.915 F1QGH9 →
D2SW95 0.914 D2SW95 →
Q9P2I0 0.914 Q9P2I0 →
Q5RDM4 0.914 Q5RDM4 →
A0JN39 0.914 A0JN39 →
Q10568 0.914 Q10568 →
B2RYD2 0.914 B2RYD2 →
Q5ZIA5 0.914 Q5ZIA5 →
Q5R922 0.914 Q5R922 →
O88506 0.914 O88506 →
Q28DS0 0.914 Q28DS0 →