MSL1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to MSL1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Impact of tdrd9 Gene Mutations in the Therapeutic Response to L-carnitine in Oligoasthenozoospermic Men	PHASE3	ACTIVE_NOT_RECRUITING
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS	PHASE2	COMPLETED
Reverse Transcriptase Inhibitors in AGS	PHASE2	COMPLETED
Genetic Studies Spermatogenic Failure	nan	COMPLETED
Identification of New Prognostic Markers for Breast Cancer.	nan	RECRUITING
Institution of an Italian Multicenter Database of Patients With Multiple Endocrine Neoplasia Type 1 (MENNET1 Database)	nan	NOT_YET_RECRUITING
The Genetics of Chiari Type I Malformation	nan	COMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan	nan	ENROLLING_BY_INVITATION
Delineation of Novel Monogenic Disorders in the United Arab Emirates Population	nan	UNKNOWN
MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder	nan	RECRUITING
Natural History Study of Smith-Magenis Syndrome	nan	ACTIVE_NOT_RECRUITING
Study of Sperm Molecular Factors Implicated in Male Fertility	nan	COMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia	nan	NOT_YET_RECRUITING
Cryopreservation of Prepubertal Testicular Tissue for Preservation of Fertility in Young Boys With Cancer	nan	RECRUITING
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy	nan	UNKNOWN
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia	nan	UNKNOWN
SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs)	nan	RECRUITING
X-chromosome Inactivation, Epigenetics and the Transcriptome	nan	COMPLETED
Genome Medical Sequencing for Gene Discovery	nan	RECRUITING
Ccf mtDNA as a Neurodegenerative Biomarker	nan	UNKNOWN
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants.	nan	UNKNOWN
Study of Metabolic Modifications in Children With Noonan Syndrome	nan	COMPLETED
Thoracic Aortic Dilatation Syndromes	nan	COMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Depressed AIRE Gene Expression Causes Immune Cell Dysfunction & Autoimmunity in Down Syndrome	nan	COMPLETED
Human MATER and Idiopathic Infertility	nan	COMPLETED
Developing Genetic Education for Smoking Cessation	nan	COMPLETED
Hirschsprung Disease Genetic Study	nan	RECRUITING
Sperm Epigenome in Hodgkin Lymphoma	nan	NOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a MSL1 binder may also engage these)

Protein	Name	Similarity
Q6PDM1	—	1.000	Q6PDM1 →
Q8BP99	—	0.999	Q8BP99 →
Q9Y4B5	—	0.997	Q9Y4B5 →
Q9JL04	—	0.996	Q9JL04 →
Q9Y6A5	—	0.996	Q9Y6A5 →
Q6PB51	—	0.995	Q6PB51 →
Q9NYF0	—	0.995	Q9NYF0 →
Q3U2K0	—	0.994	Q3U2K0 →
Q86YN6	—	0.994	Q86YN6 →
O18805	—	0.994	O18805 →
Q8BZW2	—	0.994	Q8BZW2 →
Q8TBE0	—	0.993	Q8TBE0 →
Q7TN12	—	0.993	Q7TN12 →
A6QLA6	—	0.993	A6QLA6 →
Q6PAN7	—	0.993	Q6PAN7 →
Q497V6	—	0.993	Q497V6 →
Q8TAB5	—	0.993	Q8TAB5 →
Q58CQ0	—	0.993	Q58CQ0 →
Q498S6	—	0.993	Q498S6 →
A2A9F4	—	0.993	A2A9F4 →
Q8NCN4	—	0.993	Q8NCN4 →
Q7Z591	—	0.993	Q7Z591 →
Q9Y6F6	—	0.992	Q9Y6F6 →
P48382	—	0.992	P48382 →
Q76N89	—	0.992	Q76N89 →
Q8BZ32	—	0.992	Q8BZ32 →
MIDEAS	Mitotic deacetylase-associated SANT domain protein	0.992	landscape →
Q4R2Z8	—	0.992	Q4R2Z8 →
Q5TGY3	—	0.992	Q5TGY3 →
Q96RK0	—	0.992	Q96RK0 →