CDV3

Protein CDV3 homolog · Q9UKY7 · CDV3 on Sugi Atlas →

0 patent compounds predicted against CDV3, 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 CDV3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Pembrolizumab Plus Enfortumab Vedotin in Collecting Duct and Renal Medullary Carcinoma PHASE2RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Assessing the Immunogenicity of pING-hHER3FL PHASE1ACTIVE_NOT_RECRUITING
99mTc-3PRGD2 SPECT/CT in Rheumatoid Arthritis Patients EARLY_PHASE1COMPLETED
Celiac Disease Genomic Environmental Microbiome and Metabolomic Study nanRECRUITING
The Role of DNA and RNA in NGS Analyses for Advaced Stage NSCLC Patients nanRECRUITING
Notch 1 Mutation in Chronic Lymphocytic Leukemia and Non-Hodgkin's Lymphoma Patient nanNOT_YET_RECRUITING
The Congenital Dyserythropoietic Anemia Registry (CDAR) nanRECRUITING
Search for New Genetic Mutations Major Effect in Crohn's Disease nanCOMPLETED
Development and Validation of a Nomogram for Predicting Surgery in Newly-diagnosed Crohn's Disease: a Retrospective Cohort Study nanCOMPLETED
Genetic Studies of Chronic Active Epstein-Barr Disease nanRECRUITING
Genetic Studies of Inflammatory Bowel Disease nanCOMPLETED
Genome Analysis of Human Endogenous Retroviruses (HERVs)(COVID19) nanRECRUITING
Risk Factors for the Development of Celiac Disease in Genetically Predisposed Children nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Congenital Uterine Anomalies: Identifying Cancer Associations and Genetic and Environmental Factors to Improve Clinical Care nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Genetic Determinants of Sudden Cardiac Death nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Congenital Hemolytic and Dyserythropoietic Anemias nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a CDV3 binder may also engage these)

ProteinNameSimilarity
A4PB26 1.000 A4PB26 →
Q4VAA2 0.993 Q4VAA2 →
Q6DIS2 0.992 Q6DIS2 →
Q5XIM5 0.992 Q5XIM5 →
Q7ZYA6 0.991 Q7ZYA6 →
Q5ZLH9 0.990 Q5ZLH9 →
Q7T370 0.988 Q7T370 →
Q8MMC4 0.975 Q8MMC4 →
Q92733 0.974 Q92733 →
Q8R1N0 0.974 Q8R1N0 →
Q8N3X1 0.973 Q8N3X1 →
D3ZTQ1 0.972 D3ZTQ1 →
Q6PFK1 0.972 Q6PFK1 →
Q3MHS2 0.972 Q3MHS2 →
Q96NB3 0.971 Q96NB3 →
Q6PII3 0.971 Q6PII3 →
Q3USH5 0.971 Q3USH5 →
Q9D0V7 0.971 Q9D0V7 →
Q8K039 0.971 Q8K039 →
Q6NWC9 0.970 Q6NWC9 →
Q4ADK7 0.970 Q4ADK7 →
Q9SU25 0.970 Q9SU25 →
Q8BZR9 0.970 Q8BZR9 →
O88271 0.970 O88271 →
Q12872 0.969 Q12872 →
Q8CGC4 0.969 Q8CGC4 →
O16053 0.969 O16053 →
Q53F19 0.969 Q53F19 →
Q9SAD7 0.969 Q9SAD7 →
Q6ZQ03 0.969 Q6ZQ03 →