PRRC2C — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to PRRC2C by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Evaluating Myelodysplastic Syndrome Risks in NET Patients Planned for Peptide Radionuclide Therapy	nan	RECRUITING
A Multicenter Pharmacoepidemiological Cohort on Real Life Use of Semaglutide in Adolescents or Adults With Monogenic Obesity	nan	RECRUITING
Inherited Reproductive Disorders	nan	RECRUITING
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks	nan	RECRUITING
Involvement of Endogenous Digitalis-like Compounds in Breast Cancer	nan	WITHDRAWN
Von Hippel-Lindau (VHL): Clinical Manifestations, Diagnosis, Management and Molecular Bases of Inherited Renal and Other Urologic Malignant Disorders	nan	RECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome	nan	UNKNOWN
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN)	nan	RECRUITING
Study of Usher Syndromes, Type 1 and Type 2	nan	COMPLETED
Hormonal Regulation of Puberty and Fertility	nan	COMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
CDH1 Germline Mutations in Lobular Breast Cancer	nan	COMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
Circadian Rhythms and Sleep in Familial DSPS and ASPS	nan	COMPLETED
PACAP Induced Migraine Attacks in Patients With High and Low Genetic Load	nan	COMPLETED
Mayo AVC Registry and Biobank	nan	RECRUITING
Clinically Actionable Tumor-Associated Antigens in Prostate Cancer	nan	ACTIVE_NOT_RECRUITING
Reverse Phenotyping Core	nan	ENROLLING_BY_INVITATION
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
A Study on Risk Mutations of Vulnerability Genes of Schizophrenia	nan	UNKNOWN
Genetics of Rolandic Epilepsy	nan	COMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders	nan	COMPLETED
Advancing Neurogenetic Diagnoses Through Long-Read Sequencing	nan	NOT_YET_RECRUITING
Identification of New Genes Implicated in Rare Neurosensory Diseases by Whole Exome Sequencing	nan	UNKNOWN
Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services	nan	UNKNOWN
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation	nan	UNKNOWN
Exome Analysis in Hearing Impaired Patients	nan	UNKNOWN
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study	nan	UNKNOWN

Related proteins — ESM-2 sequence neighbours (a PRRC2C binder may also engage these)

Protein	Name	Similarity
Q3TLH4	—	1.000	Q3TLH4 →
Q7TPM1	—	0.997	Q7TPM1 →
Q66J90	—	0.997	Q66J90 →
F1QIC4	—	0.996	F1QIC4 →
Q6KCD5	—	0.994	Q6KCD5 →
Q6PEI3	—	0.994	Q6PEI3 →
P0CB49	—	0.993	P0CB49 →
Q5TM26	—	0.993	Q5TM26 →
Q86TC9	—	0.993	Q86TC9 →
Q5RAU1	—	0.993	Q5RAU1 →
Q9R0I7	—	0.993	Q9R0I7 →
Q8IZ21	—	0.992	Q8IZ21 →
PPHLN1	Periphilin-1	0.992	landscape →
Q5HZJ0	—	0.992	Q5HZJ0 →
P40645	—	0.992	P40645 →
Q5JSZ5	—	0.992	Q5JSZ5 →
A0A1L8HFX9	—	0.992	A0A1L8HFX9 →
D5MCN2	—	0.992	D5MCN2 →
Q9D824	—	0.992	Q9D824 →
Q5XJD3	—	0.992	Q5XJD3 →
Q6KC79	—	0.992	Q6KC79 →
Q80TN7	—	0.992	Q80TN7 →
Q14151	—	0.992	Q14151 →
P70047	—	0.992	P70047 →
Q9ULH7	—	0.992	Q9ULH7 →
Q09801	—	0.991	Q09801 →
A0A0R4IZ84	—	0.991	A0A0R4IZ84 →
Q9XTT4	—	0.991	Q9XTT4 →
A5DLJ8	—	0.991	A5DLJ8 →
Q5TZ18	—	0.991	Q5TZ18 →