NOM1

Nucleolar MIF4G domain-containing protein 1 · Q5C9Z4 · NOM1 on Sugi Atlas →

0 patent compounds predicted against NOM1, 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 NOM1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pharmacokinetic and Tolerability Study of NFC-1 in Subjects Aged 6-17 Years With ADHD PHASE1COMPLETED
Roles of Some Non-classic Biomarkers in Pediatric Pneumonia nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder nanRECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Micro Ribosomal Nucleic Acid 155 in Non Hodgkin Lymphoma nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles 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
Clinical Study of Muenke Syndrome (FGFR3-Related Craniosynostosis) nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Investigation of Copy Number Variations and Genetic Variants in POI nanRECRUITING
Study of the Effect of Innate on the Inflammatory Response to Endotoxin nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Amplification of Zinc Finger Protein 217 Gene in Multiple Myeloma nanUNKNOWN
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
Modifying Genes in Neurofibromatosis 1 nanUNKNOWN
Genetic Determinants of Kawasaki Disease nanUNKNOWN
Predisposition Genes in Monogenic Diabetes (DIAMONO) nanCOMPLETED
Genetic Analysis Using Blood or Bone Marrow From Participants With Neuroblastoma or Noncancerous Conditions nanCOMPLETED
Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NOM1 binder may also engage these)

ProteinNameSimilarity
Q3UFM5 0.982 Q3UFM5 →
Q4R4I0 0.977 Q4R4I0 →
TERF2IP Telomeric repeat-binding factor 2-interacting protein 1 0.976 landscape →
Q496Y0 0.974 Q496Y0 →
P12755 0.974 P12755 →
Q8NFZ0 0.971 Q8NFZ0 →
Q7ZYB4 0.971 Q7ZYB4 →
F1N2W9 0.971 F1N2W9 →
Q0VCT3 0.971 Q0VCT3 →
F1R7R1 0.971 F1R7R1 →
Q6DVA0 0.970 Q6DVA0 →
Q9BWU0 0.970 Q9BWU0 →
Q80U62 0.970 Q80U62 →
Q8R1T1 0.970 Q8R1T1 →
Q2KJ58 0.969 Q2KJ58 →
A2SXS5 0.969 A2SXS5 →
Q8VDV3 0.969 Q8VDV3 →
Q9NVU0 0.969 Q9NVU0 →
Q9WU40 0.968 Q9WU40 →
Q9UPU7 0.968 Q9UPU7 →
Q8C190 0.968 Q8C190 →
O54935 0.968 O54935 →
B0KWQ2 0.968 B0KWQ2 →
Q8IYL2 0.968 Q8IYL2 →
Q02040 0.968 Q02040 →
Q8HXH0 0.968 Q8HXH0 →
Q8WVT3 0.968 Q8WVT3 →
DCUN1D3 DCN1-like protein 3 0.968 landscape →
Q8TBN0 0.968 Q8TBN0 →
Q8CC12 0.968 Q8CC12 →