FRG1

Protein FRG1 · Q14331 · FRG1 on Sugi Atlas →

0 patent compounds predicted against FRG1, 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 FRG1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Phase 1/2 Study of FRF-001, an AAV-9 Gene Therapy, in Patients With FOXG1 Syndrome (FS) PHASE1/PHASE2NOT_YET_RECRUITING
Open Trail of γIFN for Friedreich Ataxia PHASE2COMPLETED
Folate Receptor Alpha Peptide Vaccine With GM-CSF in Patients With Triple Negative Breast Cancer PHASE2COMPLETED
Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of Folate Receptor Alpha (FRα) Expressing, Platinum-sensitive Epithelial Ovarian Cancer PHASE2ACTIVE_NOT_RECRUITING
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS PHASE2COMPLETED
[18F]-AZAFOL AS POSITRON EMISSION TOMOGRAPHY (PET) TRACER in FR Positive Cancer Imaging PHASE1COMPLETED
Methylprednisolone Treatment of Friedreich Ataxia EARLY_PHASE1COMPLETED
The Development of Human Immunologic Assays Specific to Folate Receptor Antigen nanUNKNOWN
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
Von Hippel-Lindau (VHL): Clinical Manifestations, Diagnosis, Management and Molecular Bases of Inherited Renal and Other Urologic Malignant Disorders nanRECRUITING
Neurogenetics Patient Registry nanRECRUITING
Use Massive Parallel Sequencing and Exome Capture Technology to Sequence the Exome of Fanconi Anemia Children and Their Patents nanAVAILABLE
The Genetic Study of Primary Angle-Closure Glaucoma nanUNKNOWN
DeciFace: Decipher the Influence of Ethnic Backgrounds on the Facial Dysmorphic Features of Rare Mendelian Disorders nanRECRUITING
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Corrective Exercise and Rehabilitation in Fanconi Anemia: A Case Study nanCOMPLETED
Collaborative Studies on the Genetics of Asthma (CSGA) nanCOMPLETED
Efficacy of Stabilometric Platform to Improve Standing Balance in Patients With Friedreich's Ataxia nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Gene Expression in Predicting Response to Paclitaxel in Patients With Breast Cancer nanUNKNOWN
A Study to Assess Variation in Potential Biomarkers in Friedreich Ataxia nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Efferocytosis and Genomic Polymorphism in Autoimmune Diseases nanUNKNOWN
FGL2/Fibroleukin and Hepatitis C Virus Recurrence Post Liver Transplantation nanUNKNOWN
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
FRIEDREICH ATAXIA- STEROIDOGENESIS nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Genetic Study of Familial Epilepsy nanCOMPLETED
Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a FRG1 binder may also engage these)

ProteinNameSimilarity
P97376 1.000 P97376 →
Q6GLS8 0.967 Q6GLS8 →
O73747 0.966 O73747 →
Q2HJ41 0.965 Q2HJ41 →
Q28C34 0.961 Q28C34 →
Q9TS33 0.959 Q9TS33 →
Q8BM39 0.959 Q8BM39 →
Q6GMH0 0.958 Q6GMH0 →
Q9JKB8 0.958 Q9JKB8 →
Q5RE03 0.958 Q5RE03 →
Q99633 0.958 Q99633 →
Q66H99 0.958 Q66H99 →
Q5EAV6 0.958 Q5EAV6 →
A2AGL3 0.958 A2AGL3 →
Q8QFR2 0.958 Q8QFR2 →
P30957 0.958 P30957 →
RYR2 Ryanodine receptor 2 0.958 landscape →
Q6NRD0 0.957 Q6NRD0 →
Q6P4T2 0.957 Q6P4T2 →
EIF3A Eukaryotic translation initiation factor 3 subunit A 0.957 landscape →
B0LPN4 0.957 B0LPN4 →
SNRNP200 U5 small nuclear ribonucleoprotein 200 kDa helicase 0.956 landscape →
P29540 0.956 P29540 →
Q5R644 0.956 Q5R644 →
Q8N6S4 0.956 Q8N6S4 →
PRPF3 U4/U6 small nuclear ribonucleoprotein Prp3 0.956 landscape →
Q1JU68 0.955 Q1JU68 →
Q15413 0.955 Q15413 →
Q5ZMW3 0.955 Q5ZMW3 →
Q07866 0.955 Q07866 →