NOC2L

Nucleolar complex protein 2 homolog · Q9Y3T9 · NOC2L on Sugi Atlas →

0 patent compounds predicted against NOC2L, 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 NOC2L by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS PHASE2COMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Quantitative Assessment of the Etiologies of Megalencephaly Associated With a Detectable Tumor Risk nanNOT_YET_RECRUITING
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetics of Neonatal Encephalopathy and Related Disorders nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
Advancing Neurogenetic Diagnoses Through Long-Read Sequencing nanNOT_YET_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
Testing of NBIA Genes: Analysis of Genetic Heterogeneity and Validation of Mitochondrial Markers for Assessing Causality of Sequence Variants. nanCOMPLETED
The Contribution of Optical Mapping to the Characterization of Chromosomal Rearrangements in Patients With Neurodevelopmental Disorders nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Analysis Using Blood or Bone Marrow From Participants With Neuroblastoma or Noncancerous Conditions nanCOMPLETED
Modifying Genes in Neurofibromatosis 1 nanUNKNOWN
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
A Study of the Interaction Between Tumor Susceptibility Gene Glycine N-methyltransferase (GNMT) and Lung Cancer nanUNKNOWN
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Endolymphatic Sac Tumors in a Population of Patients With Von Hippel-Lindau Disease:The Natural History and Pathobiology, and a Prospective Non-Randomized Clinical Trial of Hearing Preservation Surgery in Patients With Early Stage Endolymphatic Sac Tumors nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Comparative 2-D Tumor Analysis in Familial Gliomas nanCOMPLETED
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples nanCOMPLETED
Novel Biomarkers in the Neoplastic Progression of Barrett's Esophagus nanACTIVE_NOT_RECRUITING
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Genetic Identification (ID) of Segmental Dysplastic Nevi nanWITHDRAWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NOC2L binder may also engage these)

ProteinNameSimilarity
Q9WV70 1.000 Q9WV70 →
Q3SYU1 1.000 Q3SYU1 →
MYBBP1A Myb-binding protein 1A 0.984 landscape →
D3ZND0 0.984 D3ZND0 →
Q6DRN3 0.984 Q6DRN3 →
Q8K2Z4 0.983 Q8K2Z4 →
Q9D479 0.982 Q9D479 →
Q7TPV4 0.982 Q7TPV4 →
A0JN53 0.982 A0JN53 →
P78316 0.982 P78316 →
Q3T1I9 0.981 Q3T1I9 →
Q9DC40 0.981 Q9DC40 →
TELO2 Telomere length regulation protein TEL2 homolog 0.981 landscape →
O35821 0.981 O35821 →
O70576 0.981 O70576 →
Q1JQC5 0.980 Q1JQC5 →
Q5M9G7 0.980 Q5M9G7 →
Q8C3S2 0.980 Q8C3S2 →
Q58CQ5 0.980 Q58CQ5 →
Q8R3N1 0.980 Q8R3N1 →
Q8BM55 0.980 Q8BM55 →
Q9UNS1 0.980 Q9UNS1 →
Q9Z2Y1 0.979 Q9Z2Y1 →
Q08CY4 0.979 Q08CY4 →
Q9EPK6 0.979 Q9EPK6 →
Q3UJU9 0.979 Q3UJU9 →
Q66H85 0.979 Q66H85 →
O75800 0.979 O75800 →
Q9UJY4 0.979 Q9UJY4 →
Q99M76 0.978 Q99M76 →