EXOC1 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to EXOC1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)	PHASE1/PHASE2	RECRUITING
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome	PHASE2	RECRUITING
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype	EARLY_PHASE1	COMPLETED
Thoracic Aortic Dilatation Syndromes	nan	COMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events	nan	COMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks	nan	RECRUITING
Autophagy in Systemic Lupus Erythematosus	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
A Study of Circulating Exosome Proteomics In Gallbladder Carcinoma Patients	nan	UNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus	nan	COMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Mapping Disease Pathways for Biliary Atresia	nan	RECRUITING
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms	nan	UNKNOWN
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions	nan	RECRUITING
Defective FGFR2 Signaling in the Small Airway Basal Progenitor Cells in COPD	nan	COMPLETED
MERC Proteins in Saliva and GCF in Periodontal Disease (ELISA Study)	nan	COMPLETED
Multicentric Prospective Study of Genetic and Physiopathology Concerning Dysregulation of Complement During Repeated Fetal Abortions	nan	COMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans	nan	UNKNOWN
Family Study of Melanoma in Italy	nan	COMPLETED
Whole Exome Sequencing in Coronary Artery Ectasia	nan	COMPLETED
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols	nan	COMPLETED
A Study That Collects Participant Data and Biospecimens to Analyze Pathogenic Exosomes That Mediate Increased Vascular Dementia Risk in Individuals With Herpes Zoster.	nan	RECRUITING
Monogenic Diabetes Misdiagnosed as Type 1	nan	RECRUITING
Exosome of Mesenchymal Stem Cells for Multiple Organ Dysfuntion Syndrome After Surgical Repaire of Acute Type A Aortic Dissection	nan	NOT_YET_RECRUITING
Genetic Screening and Assisted Oocyte Activation in Couples with Diminished/aberrant Embryonic Development.	nan	COMPLETED
Exome Analysis in Hearing Impaired Patients	nan	UNKNOWN

Related proteins — ESM-2 sequence neighbours (a EXOC1 binder may also engage these)

Protein	Name	Similarity
Q8R3S6	—	1.000	Q8R3S6 →
Q5ZKV9	—	0.985	Q5ZKV9 →
A6H5Z3	—	0.983	A6H5Z3 →
Q9Y2D4	—	0.983	Q9Y2D4 →
Q8TAG9	—	0.980	Q8TAG9 →
F1LSG8	—	0.978	F1LSG8 →
Q8CI71	—	0.977	Q8CI71 →
E2R766	—	0.976	E2R766 →
Q96JG6	—	0.971	Q96JG6 →
O54923	—	0.969	O54923 →
Q9Y3P9	—	0.968	Q9Y3P9 →
Q5RAN1	—	0.967	Q5RAN1 →
Q5ZLD7	—	0.965	Q5ZLD7 →
Q5VIR6	—	0.964	Q5VIR6 →
Q8CCB4	—	0.964	Q8CCB4 →
Q5R5J4	—	0.963	Q5R5J4 →
Q8R313	—	0.962	Q8R313 →
Q8VC42	—	0.962	Q8VC42 →
A2AWA9	—	0.962	A2AWA9 →
Q5EAD0	—	0.961	Q5EAD0 →
Q7Z3J2	—	0.960	Q7Z3J2 →
GPS1	COP9 signalosome complex subunit 1	0.960	landscape →
Q9TUZ0	—	0.960	Q9TUZ0 →
P42230	—	0.960	P42230 →
Q8BPU7	—	0.960	Q8BPU7 →
STAT5B	Signal transducer and activator of transcription 5B	0.960	landscape →
P42232	—	0.960	P42232 →
Q9TUM3	—	0.959	Q9TUM3 →
ELMO1	Engulfment and cell motility protein 1	0.959	landscape →
P52632	—	0.958	P52632 →