MON2

Protein MON2 homolog · Q7Z3U7 · MON2 on Sugi Atlas →

0 patent compounds predicted against MON2, 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 MON2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pharmacogenomic Evaluation of Antihypertensive Responses PHASE4COMPLETED
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Pilot Study of Familial Nonsyndromal Mondini Dysplasia nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetic Studies in Patients and Families With Infantile Spasms nanCOMPLETED
Target of Suv420h1/2 in Hepatocytes nanRECRUITING
Epidemiology of Pituitary Tumours: Prevalence of Associated Neoplasia nanUNKNOWN
The Genetics of Chiari Type I Malformation nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Stem Cell Models of Best Disease and Other Retinal Degenerative Diseases. nanCOMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Family Blood Pressure Program - GENOA nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Study of the Effect of Innate on the Inflammatory Response to Endotoxin nanRECRUITING
Bisphosphonate Therapy in MONA Spectrum Disorder nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Use of miRNAs in Growth Hormone Deficiency (GHD) nanUNKNOWN
Immune Cell Response to Stimuli nanRECRUITING
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study nanACTIVE_NOT_RECRUITING
Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases nanUNKNOWN
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a MON2 binder may also engage these)

ProteinNameSimilarity
Q80TL7 1.000 Q80TL7 →
Q6GP04 0.994 Q6GP04 →
Q29L43 0.984 Q29L43 →
Q9VLT1 0.983 Q9VLT1 →
Q9Y6D5 0.980 Q9Y6D5 →
TRRAP Transformation/transcription domain-associated protein 0.980 landscape →
O94915 0.979 O94915 →
D4A631 0.979 D4A631 →
ARFGEF1 Brefeldin A-inhibited guanine nucleotide-exchange protein 1 0.978 landscape →
A0A0R4ITC5 0.978 A0A0R4ITC5 →
P21359 0.978 P21359 →
Q9JLN9 0.977 Q9JLN9 →
Q5R6J0 0.977 Q5R6J0 →
Q7TSU1 0.976 Q7TSU1 →
A2VE70 0.976 A2VE70 →
MTOR Serine/threonine-protein kinase mTOR 0.976 landscape →
Q99P88 0.975 Q99P88 →
Q7TMY8 0.975 Q7TMY8 →
Q6PDI5 0.975 Q6PDI5 →
F4JN05 0.975 F4JN05 →
A2A5R2 0.974 A2A5R2 →
P42346 0.974 P42346 →
Q5ZL91 0.974 Q5ZL91 →
HUWE1 E3 ubiquitin-protein ligase HUWE1 0.974 landscape →
XPO5 Exportin-5 0.974 landscape →
P37199 0.973 P37199 →
Q9EPN1 0.973 Q9EPN1 →
NUP155 Nuclear pore complex protein Nup155 0.973 landscape →
Q86UW7 0.973 Q86UW7 →
Q80W92 0.973 Q80W92 →