ABHD14B — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to ABHD14B by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Study of ORGN001 (Formerly ALXN1101) in Neonates, Infants and Children With Molybdenum Cofactor Deficiency (MOCD) Type A	PHASE2/PHASE3	COMPLETED
PCD New Gene Discovery	nan	COMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome	nan	RECRUITING
Stone Disease in Children and Their Families	nan	COMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients	nan	RECRUITING
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Study on Moebius Syndrome and Congenital Facial Weakness Disorders	nan	COMPLETED
Genetic Analysis of Hereditary Non-Syndromic Oral Clefts	nan	COMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes	nan	RECRUITING
Genetic Investigation of Cancer Predisposition	nan	NOT_YET_RECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease	nan	RECRUITING
Genetic and Functional Analysis of Aplasia Cutis Congenital (ACC)	nan	RECRUITING
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease	nan	UNKNOWN
Core Stability Exercises and Hereditary Ataxia	nan	COMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
Hereditary Nonpolyposis Colorectal Cancer in Taiwan-Related Genetic Study and Clinical Applications	nan	UNKNOWN
NIAID Clinical Center Genomics Opportunity Protocol	nan	COMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions	nan	RECRUITING
Sodium Transport: Genetics and Hypertension	nan	COMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism	nan	COMPLETED
ClinSeq: A Large-Scale Medical Sequencing Clinical Research Pilot Study	nan	ACTIVE_NOT_RECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome	nan	UNKNOWN
Genetic Analysis of Parkinson's Disease	nan	COMPLETED
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Identification of an Asthma Susceptibility Gene on 3P	nan	COMPLETED
Risk Burden of Lipoprotein Metabolic Gene Haplotypes	nan	COMPLETED
Autophagy Bladder Cancer	nan	UNKNOWN
Genetic Analysis of Inherited Urologic Malignant Disorders: Collection of Samples	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a ABHD14B binder may also engage these)

Protein	Name	Similarity
Q8VCR7	—	1.000	Q8VCR7 →
Q5R816	—	1.000	Q5R816 →
A7YY28	—	1.000	A7YY28 →
Q6DGG1	—	0.991	Q6DGG1 →
Q8Z0C0	—	0.979	Q8Z0C0 →
Q63HM1	—	0.977	Q63HM1 →
P24618	—	0.977	P24618 →
C8CP46	—	0.976	C8CP46 →
Q55921	—	0.976	Q55921 →
Q8U671	—	0.976	Q8U671 →
B2JQW2	—	0.976	B2JQW2 →
B6I695	—	0.976	B6I695 →
Q2QMG2	—	0.976	Q2QMG2 →
Q8X5K0	—	0.975	Q8X5K0 →
A9IKK0	—	0.975	A9IKK0 →
Q1DDB7	—	0.975	Q1DDB7 →
Q9XB14	—	0.975	Q9XB14 →
Q0T1D4	—	0.975	Q0T1D4 →
B0BB27	—	0.975	B0BB27 →
Q6WAU1	—	0.975	Q6WAU1 →
B5Z370	—	0.975	B5Z370 →
A1WMV5	—	0.975	A1WMV5 →
Q31X73	—	0.975	Q31X73 →
Q1LV46	—	0.975	Q1LV46 →
B7L505	—	0.975	B7L505 →
Q9DCS2	—	0.975	Q9DCS2 →
Q9KWQ6	—	0.975	Q9KWQ6 →
P22862	—	0.975	P22862 →
A0A6F8RQ06	—	0.975	A0A6F8RQ06 →
B1XCN6	—	0.975	B1XCN6 →