RCN1

Reticulocalbin-1 · Q15293 · RCN1 on Sugi Atlas →

0 patent compounds predicted against RCN1, 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 RCN1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Bovine Lactoferrin to Prevent and Cure Iron Deficiency and Iron Deficiency Anemia in Complicated Pregnancies PHASE4COMPLETED
Renal Protection Using Sympathetic Denervation in Patients With Chronic Kidney Disease PHASE2UNKNOWN
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
Neutrophils as Prognostic Factors in Granulomatosis With Polyangiitis (Formerly Named Wegener's Granulomatosis) nanCOMPLETED
Rheo-Erythrocrine Dysfunction as a Biomarker for RIC Treatment in Acute Ischemic Stroke nanCOMPLETED
Immunological Profile and Clinical Characteristics of Children Diagnosed With Chronic Granulomatous Disease nanUNKNOWN
Congenital Hemolytic and Dyserythropoietic Anemias nanRECRUITING
Serum Talin-1 and Cripto-1 in Colorectal Cancer nanNOT_YET_RECRUITING
Evaluate the Effort Test as a Therapeutic Monitoring Tool in Acute Rhabdomyolyses nanCOMPLETED
Observational Study of Sepsis and Pneumonia to Develop Diagnostic Tests nanUNKNOWN
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Allergy and Immunology Natural History Study nanRECRUITING
p11 Protein Levels in Patients With Major Depressive Disorder Treated With Citalopram nanCOMPLETED
Genomic of CONgenital Sideroblastic Anemias nanRECRUITING
Serum NGAL IN Patients With Multiple Myeloma nanUNKNOWN
Diagnostic Odyssey Survey 2 nanCOMPLETED
The Congenital Dyserythropoietic Anemia Registry (CDAR) nanRECRUITING
Incidence of Iron Deficiency in Polycythemia Vera (PV) and Association With Disease Features nanUNKNOWN
GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis nanUNKNOWN
Investigations of Juvenile Neuronal Ceroid Lipofuscinosis nanRECRUITING
Recurrent Acute Myocarditis Registry nanUNKNOWN
Study of Constitutional Platelet Disease nanUNKNOWN
Utility of a Urine Screening Tool for Vitamin D Deficiency in Infants and Toddlers nanCOMPLETED
Relationship of Gestational Age and Urine Concentration of S100B in Preterm and Term Infants in the First Week of Life nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Relationship Between RAR and MACEs in AMI-CS Patients During Hospitalization nanCOMPLETED
Blood-based Biomarkers for the Prognosis of Sports Related Concussion nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Proteomics of Primary Hyperoxaluria Type 1 nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a RCN1 binder may also engage these)

ProteinNameSimilarity
Q05186 1.000 Q05186 →
Q6IP82 0.995 Q6IP82 →
O35783 0.992 O35783 →
Q7SXV9 0.991 Q7SXV9 →
Q28BT4 0.983 Q28BT4 →
B5X4E0 0.983 B5X4E0 →
Q14257 0.983 Q14257 →
Q8BP92 0.981 Q8BP92 →
B5X186 0.981 B5X186 →
Q62703 0.981 Q62703 →
O93434 0.980 O93434 →
Q2KJ39 0.979 Q2KJ39 →
Q3T0K1 0.978 Q3T0K1 →
Q4U471 0.976 Q4U471 →
I6L9G5 0.972 I6L9G5 →
Q6IQP3 0.971 Q6IQP3 →
Q96D15 0.970 Q96D15 →
O35887 0.966 O35887 →
Q8BH97 0.962 Q8BH97 →
CALU Calumenin 0.962 landscape →
J3S9D9 0.962 J3S9D9 →
Q5RDD8 0.960 Q5RDD8 →
P13213 0.956 P13213 →
Q6XLQ7 0.956 Q6XLQ7 →
P20112 0.955 P20112 →
Q8K5B2 0.954 Q8K5B2 →
Q8K5B3 0.950 Q8K5B3 →
P16975 0.950 P16975 →
A4IG32 0.948 A4IG32 →
P36377 0.946 P36377 →