Sugi Predict

Sugi Predict / Targets / CCDC22

CCDC22

Coiled-coil domain-containing protein 22 · O60826 · CCDC22 on Sugi Atlas →

0 patent compounds predicted against CCDC22, 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 CCDC22 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype EARLY_PHASE1COMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genomic Study of Congenital Malformation nanUNKNOWN
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Corpus Callosum Agenesis and Intellectual Disability nanCOMPLETED
CABP2 Patient Registry and Natural History Study nanRECRUITING
Genotype/Phenotype Correlation With Focus on Lung Function in Primary Ciliary Dyskinesia (PCD) nanUNKNOWN
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia nanCOMPLETED
Genetic Diagnosis in Congenital Cataracts nanCOMPLETED
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CCDC22 binder may also engage these)

ProteinNameSimilarity
P86182 — 1.000 P86182 →
Q9JIG7 — 1.000 Q9JIG7 →
Q1RMI8 — 1.000 Q1RMI8 →
Q4V909 — 0.993 Q4V909 →
Q28G12 — 0.992 Q28G12 →
Q6PA15 — 0.989 Q6PA15 →
Q9Z136 — 0.988 Q9Z136 →
Q6ZRF8 — 0.988 Q6ZRF8 →
Q5SPX1 — 0.988 Q5SPX1 →
Q9JL70 — 0.987 Q9JL70 →
Q8VDP4 — 0.987 Q8VDP4 →
Q571B6 — 0.987 Q571B6 →
Q9H3R5 — 0.987 Q9H3R5 →
Q3T1I9 — 0.987 Q3T1I9 →
Q9EP53 — 0.987 Q9EP53 →
Q5U3A8 — 0.987 Q5U3A8 →
Q5JU67 — 0.987 Q5JU67 →
Q7PZ96 — 0.987 Q7PZ96 →
Q8TF30 — 0.986 Q8TF30 →
Q9CZX2 — 0.986 Q9CZX2 →
O75800 — 0.986 O75800 →
Q2TAC2 — 0.986 Q2TAC2 →
Q96ST8 — 0.985 Q96ST8 →
Q9D3V1 — 0.985 Q9D3V1 →
A1A4J7 — 0.985 A1A4J7 →
Q96C34 — 0.985 Q96C34 →
A0JNG4 — 0.985 A0JNG4 →
A2BID5 — 0.985 A2BID5 →
Q17Q97 — 0.984 Q17Q97 →
D3ZND0 — 0.984 D3ZND0 →