THUMPD1 — patent landscape

Top predicted compounds (top 20 by supporting neighbours, then confidence)

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to THUMPD1 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Copper Histidine Therapy for Menkes Diseases	PHASE1/PHASE2	COMPLETED
Effect of Gemfibrozil on Serum Glycosylphosphatidylinositol (GPI) Phospholipase D and Triglycerides	PHASE1	COMPLETED
PCD New Gene Discovery	nan	COMPLETED
TL1A Expression in Psoriatic Skin	nan	UNKNOWN
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer	nan	COMPLETED
Role of Sorcin and Annexin A3 in Breast Cancer Patients	nan	UNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm	nan	COMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome.	nan	COMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes	nan	RECRUITING
Molecular Studies on Hereditary Haemorrhagic Telangiectasia Families	nan	RECRUITING
Identification of New FTLD Genes	nan	UNKNOWN
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Protein Expression in Tumor Tissue Samples From Patients With Cancer of the Oropharynx	nan	COMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease	nan	ACTIVE_NOT_RECRUITING
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy	nan	COMPLETED
hCAP18 Levels and Vitamin D Deficiency in Healthy Subjects	nan	COMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome	nan	RECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis	nan	COMPLETED
The Genetic Basis of Inherited Neurologic Deficits in People With Schizophrenia	nan	COMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease	nan	UNKNOWN
Autophagy Bladder Cancer	nan	UNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
Genetics of Cardiovascular and Neuromuscular Disease	nan	RECRUITING
A Gene Hunting Study for Familial Papillary Thyroid Cancer	nan	ACTIVE_NOT_RECRUITING

Related proteins — ESM-2 sequence neighbours (a THUMPD1 binder may also engage these)

Protein	Name	Similarity
Q99J36	—	0.998	Q99J36 →
Q24K03	—	0.997	Q24K03 →
Q6GR37	—	0.968	Q6GR37 →
NOM1	Nucleolar MIF4G domain-containing protein 1	0.962	landscape →
F1N2W9	—	0.962	F1N2W9 →
Q9CZT6	—	0.961	Q9CZT6 →
Q2T9Y1	—	0.961	Q2T9Y1 →
Q2KHI9	—	0.961	Q2KHI9 →
F1M5F3	—	0.960	F1M5F3 →
Q9NXL9	—	0.960	Q9NXL9 →
Q4R578	—	0.960	Q4R578 →
F1QDI9	—	0.959	F1QDI9 →
Q5ZIA0	—	0.958	Q5ZIA0 →
A5A6J5	—	0.958	A5A6J5 →
Q5R905	—	0.958	Q5R905 →
P61798	—	0.957	P61798 →
Q15014	—	0.957	Q15014 →
Q9BQ75	—	0.957	Q9BQ75 →
Q5R4N7	—	0.957	Q5R4N7 →
Q6QI89	—	0.956	Q6QI89 →
I0IUP4	—	0.956	I0IUP4 →
PARN	Poly(A)-specific ribonuclease PARN	0.956	landscape →
Q1HFZ0	—	0.956	Q1HFZ0 →
Q9R0Q4	—	0.955	Q9R0Q4 →
Q496Y0	—	0.955	Q496Y0 →
Q5FVR6	—	0.955	Q5FVR6 →
Q5RC51	—	0.954	Q5RC51 →
Q8VDG3	—	0.954	Q8VDG3 →
NSUN2	RNA cytosine C(5)-methyltransferase NSUN2	0.954	landscape →
Q8NFZ0	—	0.952	Q8NFZ0 →