POU2F2

POU domain, class 2, transcription factor 2 · P09086 · POU2F2 on Sugi Atlas →

6,354 patent compounds predicted against POU2F2, 3,988 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours
SCHEMBL82602 SCHEMBL82602 0.51 9/20
SCHEMBL2187039 SCHEMBL2187039 0.44 8/20
SCHEMBL81275 SCHEMBL81275 0.50 7/20
SCHEMBL92953 SCHEMBL92953 0.48 4/20
SCHEMBL3522619 SCHEMBL3522619 0.48 4/20
SCHEMBL2186404 SCHEMBL2186404 0.47 4/20
SCHEMBL3528486 SCHEMBL3528486 0.43 4/20
SCHEMBL3528387 SCHEMBL3528387 0.47 3/20
SCHEMBL2186003 SCHEMBL2186003 0.45 3/20
SCHEMBL3525535 SCHEMBL3525535 0.41 3/20
SCHEMBL2187245 SCHEMBL2187245 0.47 2/20
SCHEMBL3527644 SCHEMBL3527644 0.47 2/20
SCHEMBL965846 SCHEMBL965846 0.43 2/20
SCHEMBL1242575 SCHEMBL1242575 0.38 2/20
Linagliptin Linagliptin (SCHEMBL160188) 1.00 1/20
Linagliptin Linagliptin (SCHEMBL195962) 1.00 1/20
Linagliptin Linagliptin (SCHEMBL637238) 1.00 1/20
SCHEMBL1771687 SCHEMBL1771687 0.88 1/20
SCHEMBL1771688 SCHEMBL1771688 0.88 1/20
SCHEMBL638034 SCHEMBL638034 0.87 1/20

Clinical trials — most relevant to POU2F2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Dose Clinical Trial of Guanfacine Extended Release for the Reduction of Aggression and Self-injuries Behavior Associated With Prader-Willi Syndrome PHASE4WITHDRAWN
Mechanisms of Lipodystrophy in HIV-Infected Pateints PHASE4COMPLETED
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
Value of Using Pioglitazone in Chronic Myeloid Leukemia Treatment PHASE2COMPLETED
Evaluation of a Cancer Lysate Vaccine and Montanide (Registered Trademark) ISA-51 VG With or Without the IL-15 Super-Agonist N-803 as Adjuvant Therapy for PD-L1 Negative Non-Small Cell Lung Cancer PHASE1/PHASE2SUSPENDED
Treatment Duration Increment and Pharmacodynamic Study of CX-4945 in Patients With Basal Cell Carcinoma (BCC) PHASE1COMPLETED
Epigenomic Profiling of Circulating Cell-Free DNA (cfDNA) to Characterize the Dynamic Evolution of Molecular Subtypes in Extensive-Stage Small Cell Lung Cancer During First-Line Chemoimmunotherapy nanNOT_YET_RECRUITING
Natural History Study of GATA2 Deficiency and Related Disorders nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants. nanUNKNOWN
RORC Genetic Polymorphism of Rheumatoid Arthritis nanCOMPLETED
The Role of TBX3 in Human ES Cell Differentiation nanWITHDRAWN
Influence of OCTN2 Variants on Carnitine Status and Plasma Triglycerides nanCOMPLETED
Natural History of Thyroid Function Disorders nanRECRUITING
EKLF Gene Expression in β-thalassemia nanNOT_YET_RECRUITING
Otoferlin Patient Registry and Natural History Study nanRECRUITING
Prognostic Value of Protein IMP3 Expression in Cervical Cancer nanCOMPLETED
Family Resilience Initiative Research Program nanUNKNOWN
Development of IPS from Donated Somatic Cells of Patients with Neurological Diseases nanRECRUITING
MR Elastography in Intracranial Lesions: Feasibility & Accuracy nanACTIVE_NOT_RECRUITING
Azoospermia Patients nanRECRUITING
Effect of Post Covid-19 Hypoxia on Placenta of Normal Pregnant Women: A Possible Role of Hypoxia Inducible Factor-1α. nanUNKNOWN
Pathogenic Insights and Search for Biomarkers in RFC1-ataxia/CANVAS nanRECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
EPIgenetics and in Vivo Resistance of Chronic Myeloid Leukemia Stem Cells to Tyrosine Kinase Inhibitors nanUNKNOWN
Association of Formaldehyde Exposure to Myeloid Leukemia in Workers in Guangdong, China nanCOMPLETED
Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a POU2F2 binder may also engage these)

ProteinNameSimilarity
Q29013 1.000 Q29013 →
P31362 1.000 P31362 →
Q00196 1.000 Q00196 →
P42571 1.000 P42571 →
P62515 0.999 P62515 →
P49335 0.998 P49335 →
P62516 0.998 P62516 →
P23899 0.997 P23899 →
P22361 0.997 P22361 →
Q90867 0.996 Q90867 →
Q90270 0.996 Q90270 →
P24610 0.996 P24610 →
P20823 0.995 P20823 →
Q03365 0.995 Q03365 →
Q58NQ4 0.995 Q58NQ4 →
P27889 0.995 P27889 →
Q80TZ9 0.995 Q80TZ9 →
Q812B1 0.994 Q812B1 →
O95096 0.994 O95096 →
P35680 0.994 P35680 →
P20912 0.994 P20912 →
Q9H334 0.994 Q9H334 →
Q62255 0.994 Q62255 →
Q98876 0.994 Q98876 →
P31363 0.994 P31363 →
Q5RER5 0.994 Q5RER5 →
P25425 0.993 P25425 →
P48031 0.993 P48031 →
Q6F2E4 0.993 Q6F2E4 →
A2D4R4 0.993 A2D4R4 →