Sugi Predict

Sugi Predict / Targets / PRR12

PRR12

Proline-rich protein 12 · Q9ULL5 · PRR12 on Sugi Atlas →

0 patent compounds predicted against PRR12, 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 PRR12 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
CB-PRP in Retinitis Pigmentosa and Dry Age-related Macular Degeneration PHASE3COMPLETED
Management of Retinitis Pigmentosa Via Combination of Wharton's Jelly-derived Mesenchymal Stem Cells and Magnovision PHASE3COMPLETED
The Phosphodiesterase 4 Inhibitor Roflumilast as an Adjunct to Antidepressants in Major Depressive Disorder Patients PHASE1/PHASE2WITHDRAWN
Testing the Combination of MLN4924 (Pevonedistat), Carboplatin, and Paclitaxel in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) Who Have Previously Been Treated With Immunotherapy PHASE2ACTIVE_NOT_RECRUITING
A Study Evaluating Megestrol Acetate Modulation in Hormone Receptor Positive Advanced Breast Cancer PHASE2UNKNOWN
Study of Oral Minocycline in Treating Bilateral Cystoid Macular Edema Associated With Retinitis Pigmentosa PHASE1/PHASE2COMPLETED
Evaluation of Safety of Ciliary Neurotrophic Factor Implants in the Eye PHASE1COMPLETED
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) nanCOMPLETED
Lymphoid Tyrosine Phosphatase Gene Polymorphisms in Inflammatory Bowel Disease nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Evaluation of Vasopressin in the Vessels of Ovarian Neoplasms nanCOMPLETED
The Effect of Laparoscopic Sleeve Gastrectomy on Blood Phoenixin-14 Levels nanCOMPLETED
Aswan Heart Centre - Egyptian Healthy Volunteers nanRECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Predictive Value of Maternal Blood Protein Signatures in Preterm Birth nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Management of Cystoid Macular Edema Secondary to Retinitis Pigmentosa Via Subliminal Micropulse Yellow Laser nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Characterizing a 5P-Linked BHR Susceptibility Locus nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Quantification of GADD34 Expression in RA nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a PRR12 binder may also engage these)

ProteinNameSimilarity
E9PYL2 — 1.000 E9PYL2 →
O15417 — 0.995 O15417 →
Q5TGY3 — 0.993 Q5TGY3 →
P31310 — 0.992 P31310 →
Q80WC3 — 0.991 Q80WC3 →
M0R6D8 — 0.990 M0R6D8 →
Q2HJ78 — 0.990 Q2HJ78 →
Q6PAL7 — 0.990 Q6PAL7 →
A2T6H5 — 0.989 A2T6H5 →
Q9JKQ4 — 0.989 Q9JKQ4 →
A1YG01 — 0.989 A1YG01 →
Q9P1Z0 — 0.989 Q9P1Z0 →
Q9P281 — 0.989 Q9P281 →
P81067 — 0.989 P81067 →
P78411 — 0.989 P78411 →
P49715 — 0.988 P49715 →
P50548 — 0.988 P50548 →
P02831 — 0.988 P02831 →
Q5TM26 — 0.987 Q5TM26 →
Q8MIP2 — 0.987 Q8MIP2 →
P81068 — 0.987 P81068 →
Q08DG7 — 0.987 Q08DG7 →
P57073 — 0.987 P57073 →
A2T7H5 — 0.987 A2T7H5 →
P14651 — 0.987 P14651 →
Q04888 — 0.987 Q04888 →
Q61572 — 0.986 Q61572 →
O35126 — 0.986 O35126 →
P78415 — 0.986 P78415 →
O95886 — 0.986 O95886 →