ZNF277 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to ZNF277 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Safety and Dose Escalation Study of Zinc Supplementation in Critically Ill Children	PHASE1/PHASE2	COMPLETED
ZR-CHOP in DLBCL With Specific Gene Abnormality	PHASE2	UNKNOWN
Amplification of Zinc Finger Protein 217 Gene in Multiple Myeloma	nan	UNKNOWN
Gene Expression in Predicting Response to Paclitaxel in Patients With Breast Cancer	nan	UNKNOWN
Study of Tazemetostat in Adults With Follicular Lymphoma Previously Treated With at Least Two Therapies	nan	WITHDRAWN
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia	nan	UNKNOWN
Zinc and the Synthesis of Zinc Binding Proteins (Protocol B)	nan	COMPLETED
Study of Gene Associations and Infertility	nan	ENROLLING_BY_INVITATION
Novel Biomarkers in the Neoplastic Progression of Barrett's Esophagus	nan	ACTIVE_NOT_RECRUITING
Linkage Study in Familial Pulmonary Fibrosis	nan	COMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization	nan	COMPLETED
Genetic Studies of Inflammatory Bowel Disease	nan	COMPLETED
Family Myopia Study	nan	COMPLETED
A Gene Hunting Study for Familial Papillary Thyroid Cancer	nan	ACTIVE_NOT_RECRUITING
Clinical, Radiological, Histologic and Molecular Features of a Cohort of Melanocytic Tumors of the Central Nervous System	nan	UNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome.	nan	COMPLETED
H19 in Acute Lymphoblastic Leukemia.	nan	UNKNOWN
Mechanisms of Immune Deficiency	nan	UNKNOWN
Detection of IKZF1 Deletion Mutation in Patients With Acute Lymphoblastic Leukemia and Its Impact in Therapy	nan	UNKNOWN
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders	nan	COMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions	nan	COMPLETED
The Etiology and Progression of Brain Tumors	nan	COMPLETED
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy	nan	COMPLETED
Protocol to Examine Methylation of Tumor Suppression Genes in Women at High Risk of Developing Breast Cancer	nan	COMPLETED
Characterization of Methylation Pattern in Human Germ Cells of Patients Undergoing ICSI Treatment	nan	COMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives	nan	UNKNOWN
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Rolandic Epilepsy Genomewide Association International Study	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a ZNF277 binder may also engage these)

Protein	Name	Similarity
E9Q6D6	—	0.983	E9Q6D6 →
Q8IWR0	—	0.968	Q8IWR0 →
Q8NFZ0	—	0.967	Q8NFZ0 →
SHPRH	E3 ubiquitin-protein ligase SHPRH	0.965	landscape →
Q91W96	—	0.964	Q91W96 →
Q5VUG0	—	0.964	Q5VUG0 →
Q69Z66	—	0.964	Q69Z66 →
Q5F3F2	—	0.964	Q5F3F2 →
Q5RED8	—	0.964	Q5RED8 →
P48553	—	0.963	P48553 →
Q7TPQ3	—	0.963	Q7TPQ3 →
Q9ESL4	—	0.962	Q9ESL4 →
Q8IZC4	—	0.962	Q8IZC4 →
Q1RMU2	—	0.962	Q1RMU2 →
Q9UPW5	—	0.962	Q9UPW5 →
GTF3C3	General transcription factor 3C polypeptide 3	0.962	landscape →
Q3ZBT2	—	0.962	Q3ZBT2 →
Q8BXK4	—	0.962	Q8BXK4 →
F1R7R1	—	0.962	F1R7R1 →
B0KWQ2	—	0.962	B0KWQ2 →
Q6GR37	—	0.961	Q6GR37 →
A2RT67	—	0.961	A2RT67 →
Q641K1	—	0.961	Q641K1 →
Q2HJ90	—	0.960	Q2HJ90 →
Q9NVU0	—	0.960	Q9NVU0 →
Q5T7W7	—	0.960	Q5T7W7 →
Q69ZK0	—	0.960	Q69ZK0 →
Q8IWV8	—	0.960	Q8IWV8 →
F1ND48	—	0.960	F1ND48 →
Q8WWQ0	—	0.960	Q8WWQ0 →