Sugi Predict

Sugi Predict / Targets / MNS1

MNS1

Meiosis-specific nuclear structural protein 1 · Q8NEH6 · MNS1 on Sugi Atlas →

0 patent compounds predicted against MNS1, 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 MNS1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment With HMG-COA Reductase Inhibitor of Growth and Bone Abnormalities in Children With Noonan Syndrome PHASE3COMPLETED
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men PHASE3ACTIVE_NOT_RECRUITING
Phase II Trial of Lonafarnib (a Farnesyltransferase Inhibitor) for Progeria PHASE2COMPLETED
Breakpoint Analysis of de Novo Apparently Balanced Chromosomal Translocations EARLY_PHASE1COMPLETED
The Role of Maspin in Colorectal Carcinoma, an Immunohistochemical Study nanNOT_YET_RECRUITING
Natural History Study of Smith-Magenis Syndrome nanACTIVE_NOT_RECRUITING
Study of Synapsis and Recombination in Male Meiosis and the Implications in Infertility nanCOMPLETED
Importance of the Microtubule Cytoskeleton in Oocyte Competence nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections nanCOMPLETED
Investigation of Copy Number Variations and Genetic Variants in POI nanRECRUITING
Enhanced Linkage Maps From Family-Based Genetics Studies nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Institution of an Italian Multicenter Database of Patients With Multiple Endocrine Neoplasia Type 1 (MENNET1 Database) nanNOT_YET_RECRUITING
Human MATER and Idiopathic Infertility nanCOMPLETED
The Genetics of Chiari Type I Malformation nanCOMPLETED
Predisposition Genes in Monogenic Diabetes (DIAMONO) nanCOMPLETED
MNGIE Natural History Study nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Genetic Studies Spermatogenic Failure nanCOMPLETED
Study of the Effect of Innate on the Inflammatory Response to Endotoxin nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Cerebellar Mutism Syndrome Study nanRECRUITING
Prospective Genetic Study in Patients With Ovarian Insufficiency nanUNKNOWN
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
Identifying Maturity-onset Diabetes of the Young in Emirati Patients nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a MNS1 binder may also engage these)

ProteinNameSimilarity
Q4R7T8 — 1.000 Q4R7T8 →
Q6AXQ8 — 1.000 Q6AXQ8 →
Q61884 — 1.000 Q61884 →
Q2KIQ2 — 1.000 Q2KIQ2 →
Q6PBA8 — 0.996 Q6PBA8 →
A4IJ21 — 0.994 A4IJ21 →
Q9UL16 — 0.993 Q9UL16 →
Q9D9U9 — 0.992 Q9D9U9 →
E1BJL9 — 0.990 E1BJL9 →
A0A974E306 — 0.989 A0A974E306 →
F1N7G5 — 0.989 F1N7G5 →
A0JLY1 — 0.988 A0JLY1 →
A0A480NP79 — 0.987 A0A480NP79 →
Q9D439 — 0.986 Q9D439 →
Q32LN4 — 0.986 Q32LN4 →
A0AUT1 — 0.986 A0AUT1 →
Q9BT92 — 0.986 Q9BT92 →
Q5RE49 — 0.985 Q5RE49 →
Q0VFZ6 — 0.985 Q0VFZ6 →
Q96M91 — 0.984 Q96M91 →
Q3TVW5 — 0.984 Q3TVW5 →
A0A0R4IFG5 — 0.982 A0A0R4IFG5 →
A8I9E8 — 0.977 A8I9E8 →
Q1RM03 — 0.975 Q1RM03 →
Q9D0B8 — 0.974 Q9D0B8 →
A8IRJ7 — 0.974 A8IRJ7 →
Q6AYL4 — 0.968 Q6AYL4 →
Q8N443 — 0.968 Q8N443 →
Q0VC09 — 0.967 Q0VC09 →
Q6AXN9 — 0.967 Q6AXN9 →