CCDC47

PAT complex subunit CCDC47 · Q96A33 · CCDC47 on Sugi Atlas →

0 patent compounds predicted against CCDC47, 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 CCDC47 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Phenoxybenzamine Versus Doxazosin in PCC Patients PHASE4COMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Genetics of Familial Testicular Cancer nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Genomic Study of Congenital Malformation nanUNKNOWN
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
Delineation of Novel Monogenic Disorders in the United Arab Emirates Population nanUNKNOWN
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Inherited Reproductive Disorders nanRECRUITING
Von Hippel-Lindau (VHL): Clinical Manifestations, Diagnosis, Management and Molecular Bases of Inherited Renal and Other Urologic Malignant Disorders nanRECRUITING
Hereditary Nonpolyposis Colorectal Cancer in Taiwan-Related Genetic Study and Clinical Applications nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Primary Ciliary Dyskinesia in Adult Bronchiectasis nanNOT_YET_RECRUITING
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CCDC47 binder may also engage these)

ProteinNameSimilarity
A0A8I3P7X4 1.000 A0A8I3P7X4 →
Q5U2X6 1.000 Q5U2X6 →
P0C204 1.000 P0C204 →
Q5RCI4 1.000 Q5RCI4 →
Q9D024 1.000 Q9D024 →
Q3ZC50 1.000 Q3ZC50 →
Q6AZI2 1.000 Q6AZI2 →
Q66I12 1.000 Q66I12 →
Q3SYW6 0.984 Q3SYW6 →
Q6IVW0 0.984 Q6IVW0 →
Q94CC0 0.984 Q94CC0 →
Q9ERA6 0.982 Q9ERA6 →
Q4U0Y4 0.982 Q4U0Y4 →
Q6P1V4 0.981 Q6P1V4 →
Q8R310 0.981 Q8R310 →
EIF3C Eukaryotic translation initiation factor 3 subunit C 0.981 landscape →
B5ME19 0.981 B5ME19 →
B3MIF1 0.981 B3MIF1 →
Q7ZY81 0.981 Q7ZY81 →
B4LNA1 0.981 B4LNA1 →
Q960E8 0.981 Q960E8 →
B3NML0 0.981 B3NML0 →
Q5RAT8 0.981 Q5RAT8 →
NAT10 RNA cytidine acetyltransferase 0.981 landscape →
A1XD94 0.981 A1XD94 →
Q8IQ70 0.981 Q8IQ70 →
O08837 0.980 O08837 →
Q8CCP0 0.980 Q8CCP0 →
Q5U2Y6 0.980 Q5U2Y6 →
A1XD95 0.980 A1XD95 →