KATNAL2 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to KATNAL2 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation	PHASE2/PHASE3	UNKNOWN
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS	PHASE2	COMPLETED
Trial of the Histone-Deacetylase Inhibitor ITF2357 Followed by Mechlorethamine in Relapsed/Refractory Hodgkin's Lymphoma	PHASE1/PHASE2	COMPLETED
A Phase I Study of Belinostat in Combination With Cisplatin and Etoposide in Adults With Small Cell Lung Carcinoma and Other Advanced Cancers	PHASE1	COMPLETED
Pediatric Reporting of Adult-Onset Genomic Results	EARLY_PHASE1	COMPLETED
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype	EARLY_PHASE1	COMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia	nan	RECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Autophagy in Systemic Lupus Erythematosus	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Clinical and Genetic Examinations of Dilated Cardiomyopathy	nan	COMPLETED
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Studying The Role of Key Epigenetic Mediators in Breast Cancer Patients	nan	RECRUITING
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism	nan	COMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases	nan	UNKNOWN
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders	nan	COMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis.	nan	COMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia	nan	COMPLETED
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children	nan	COMPLETED
Hereditary Tubulointerstitial Nephritis	nan	COMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan	nan	ENROLLING_BY_INVITATION
Stone Disease in Children and Their Families	nan	COMPLETED
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants	nan	RECRUITING
Identification of New FTLD Genes	nan	UNKNOWN
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia	nan	UNKNOWN
Target of Suv420h1/2 in Hepatocytes	nan	RECRUITING
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia	nan	RECRUITING
Alzheimer's Disease Genetics Study	nan	RECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a KATNAL2 binder may also engage these)

Protein	Name	Similarity
Q9D3R6	—	1.000	Q9D3R6 →
Q3B8D5	—	1.000	Q3B8D5 →
A0JMA9	—	1.000	A0JMA9 →
Q6E0V2	—	1.000	Q6E0V2 →
Q9VQN8	—	1.000	Q9VQN8 →
Q8CDM1	—	1.000	Q8CDM1 →
Q9WV86	—	1.000	Q9WV86 →
KATNA1	Katanin p60 ATPase-containing subunit A1	1.000	landscape →
Q1HGK7	—	1.000	Q1HGK7 →
O43078	—	0.999	O43078 →
Q05AS3	—	0.999	Q05AS3 →
B3M301	—	0.998	B3M301 →
Q6P158	—	0.998	Q6P158 →
Q9LX30	—	0.997	Q9LX30 →
O14114	—	0.997	O14114 →
Q4R407	—	0.997	Q4R407 →
Q6AZT2	—	0.997	Q6AZT2 →
B4NBP4	—	0.997	B4NBP4 →
A6QQR4	—	0.997	A6QQR4 →
Q6GX84	—	0.997	Q6GX84 →
Q0IIR9	—	0.996	Q0IIR9 →
Q9AWM8	—	0.996	Q9AWM8 →
DHX29	ATP-dependent RNA helicase DHX29	0.996	landscape →
Q9LET7	—	0.996	Q9LET7 →
P54816	—	0.996	P54816 →
Q9DBY8	—	0.996	Q9DBY8 →
F4IV45	—	0.996	F4IV45 →
A8X0L9	—	0.996	A8X0L9 →
Q9W3D3	—	0.996	Q9W3D3 →
Q9Z1N2	—	0.996	Q9Z1N2 →