TTC14

Tetratricopeptide repeat protein 14 · Q96N46 · TTC14 on Sugi Atlas →

0 patent compounds predicted against TTC14, 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 TTC14 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Sirolimus Treatment in Patients With Autosomal Dominant Polycystic Kidney Disease: Renal Efficacy and Safety PHASE2COMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Amplification of Zinc Finger Protein 217 Gene in Multiple Myeloma nanUNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
A Family Study of Copy Number Variations in Patients With Autism Spectrum Disorder nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Ataxia GAA-FGF14 - Descriptive Genetic and Clinical Study nanACTIVE_NOT_RECRUITING
Multi-Dimensional Genomic Dissection of Ring Chromosome 14 Syndrome nanACTIVE_NOT_RECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Efficacy of Cognitive Rehabilitation Using Virtual Reality and Computer-based Cognitive Stimulation on Cognitive Impairment Associated to Movement Disorders nanCOMPLETED
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Multidisciplinary Evaluation and a Genome-wide Analysis in a Cohort of Idiopathic Short Stature Patients nanRECRUITING
Advancing Neurogenetic Diagnoses Through Long-Read Sequencing nanNOT_YET_RECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a TTC14 binder may also engage these)

ProteinNameSimilarity
Q9CSP9 1.000 Q9CSP9 →
P97868 0.995 P97868 →
P38806 0.993 P38806 →
Q9VGU5 0.992 Q9VGU5 →
Q6H7U2 0.992 Q6H7U2 →
Q8WML3 0.991 Q8WML3 →
Q7YZA2 0.991 Q7YZA2 →
A6QP06 0.991 A6QP06 →
Q3MJK5 0.991 Q3MJK5 →
Q76FK4 0.991 Q76FK4 →
Q9NRR4 0.991 Q9NRR4 →
Q14AX6 0.991 Q14AX6 →
Q5TKR9 0.991 Q5TKR9 →
Q8N3Z6 0.990 Q8N3Z6 →
Q8BMD7 0.990 Q8BMD7 →
Q92539 0.990 Q92539 →
BPTF Nucleosome-remodeling factor subunit BPTF 0.990 landscape →
P61406 0.990 P61406 →
Q5HZJ0 0.990 Q5HZJ0 →
O23273 0.990 O23273 →
Q6E3D4 0.990 Q6E3D4 →
B5E0H4 0.990 B5E0H4 →
Q8RWK8 0.990 Q8RWK8 →
F4K4J0 0.990 F4K4J0 →
O14161 0.989 O14161 →
A7YDW0 0.989 A7YDW0 →
Q99PI5 0.989 Q99PI5 →
Q5SVQ0 0.989 Q5SVQ0 →
A7TQN2 0.989 A7TQN2 →
Q922M5 0.989 Q922M5 →