PRRC2A

Protein PRRC2A · P48634 · PRRC2A on Sugi Atlas →

0 patent compounds predicted against PRRC2A, 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 PRRC2A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Evaluating Myelodysplastic Syndrome Risks in NET Patients Planned for Peptide Radionuclide Therapy nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Inherited Reproductive Disorders nanRECRUITING
A Study on Risk Mutations of Vulnerability Genes of Schizophrenia nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Study of Usher Syndromes, Type 1 and Type 2 nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study nanUNKNOWN
Genetics of Rolandic Epilepsy nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Affective Touch, Hedonia and Suicidal Behavior nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Defining the Brain Phenotype of Children With Williams Syndrome nanRECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
A Multicenter Pharmacoepidemiological Cohort on Real Life Use of Semaglutide in Adolescents or Adults With Monogenic Obesity nanRECRUITING
Acute Pain Genomic Study nanCOMPLETED
Natural History Study of Smith-Magenis Syndrome nanACTIVE_NOT_RECRUITING
Circadian Rhythms and Sleep in Familial DSPS and ASPS nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex nanCOMPLETED
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Effects of Positive Energy Balance and Exercise on Appetite Hormones in Sedentary Men and Women nanCOMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) nanCOMPLETED
Rolandic Epilepsy Genomewide Association International Study nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a PRRC2A binder may also engage these)

ProteinNameSimilarity
Q5TM26 1.000 Q5TM26 →
Q6MG48 1.000 Q6MG48 →
Q7TSC1 1.000 Q7TSC1 →
SETD1B Histone-lysine N-methyltransferase SETD1B 0.996 landscape →
Q7TPM1 0.995 Q7TPM1 →
PRRC2C Protein PRRC2C 0.993 landscape →
TET3 Methylcytosine dioxygenase TET3 0.993 landscape →
Q8CFT2 0.993 Q8CFT2 →
Q66J90 0.992 Q66J90 →
Q6PEI3 0.991 Q6PEI3 →
F1QIC4 0.991 F1QIC4 →
Q5JSZ5 0.991 Q5JSZ5 →
SETD1A Histone-lysine N-methyltransferase SETD1A 0.991 landscape →
Q96IZ0 0.990 Q96IZ0 →
Q9R0I7 0.990 Q9R0I7 →
P97868 0.990 P97868 →
Q5XJD3 0.990 Q5XJD3 →
P0CB49 0.990 P0CB49 →
Q96L91 0.990 Q96L91 →
Q9Y2H5 0.989 Q9Y2H5 →
Q5YCW1 0.989 Q5YCW1 →
Q6NZJ6 0.989 Q6NZJ6 →
Q8C3W1 0.989 Q8C3W1 →
P78414 0.989 P78414 →
O95886 0.989 O95886 →
O08919 0.988 O08919 →
CBX4 E3 SUMO-protein ligase CBX4 0.988 landscape →
Q5S6V2 0.988 Q5S6V2 →
Q7TN02 0.988 Q7TN02 →
Q14151 0.988 Q14151 →