NIPSNAP3A

Protein NipSnap homolog 3A · Q9UFN0 · NIPSNAP3A on Sugi Atlas →

0 patent compounds predicted against NIPSNAP3A, 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 NIPSNAP3A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders nanRECRUITING
Non-invasive Prenatal Diagnosis of Monogenic Disorders by Linked-reads Technology nanCOMPLETED
The 3q29 Deletion and 3q29 Duplication: Architecture of Behavioral Phenotypes nanRECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Non Ivasive Prenatal Diagnosis (NIPD) of Cystic Fibrosis nanUNKNOWN
Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo) nanWITHDRAWN
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Defining an Obesity QTL on Chromosome 3q nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Diagnosis of Prader-Willi Syndrome and Angelman Syndrome nanCOMPLETED
Non Invasive Prenatal Testing (NIPT) of Single-gene Disorders nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
CoMPaSS-NMD - Computational Models for New Patients Stratification Strategies of HNMD nanENROLLING_BY_INVITATION
Screening for Genes in Patients With Congenital Neutropenia nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Nerve Ultrasound in Acquired and Genetic Sensory Neuronopathies nanNOT_YET_RECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Biocollection of Rare Pediatric-onset of Autoimmune and Autoinflammatory Diseases nanRECRUITING
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
18F-FDG PET/TC in TIR3A e TIR3B nanENROLLING_BY_INVITATION
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Study of Blood Samples From High-Risk Postmenopausal Women Who Received Treatment on Breast Cancer Prevention Clinical Trials NSABP-P-1 or NSABP-P-2 nanUNKNOWN
The Efficiency of Postoperative Interferon-alpha Treatment in p48 Positive Patients With Hepatocellular Carcinoma nanWITHDRAWN
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease. nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a NIPSNAP3A binder may also engage these)

ProteinNameSimilarity
Q5RAA9 1.000 Q5RAA9 →
Q9CQE1 0.999 Q9CQE1 →
Q9BS92 0.999 Q9BS92 →
Q9VXK0 0.973 Q9VXK0 →
O55126 0.967 O55126 →
O55125 0.964 O55125 →
NIPSNAP1 Protein NipSnap homolog 1 0.963 landscape →
F6NVH9 0.959 F6NVH9 →
Q9PU58 0.959 Q9PU58 →
F4JP46 0.956 F4JP46 →
O75323 0.954 O75323 →
Q93YQ3 0.952 Q93YQ3 →
Q9SK66 0.951 Q9SK66 →
Q0MQB7 0.949 Q0MQB7 →
Q99LC3 0.948 Q99LC3 →
Q0MQB6 0.948 Q0MQB6 →
P0CB89 0.948 P0CB89 →
Q64HZ8 0.948 Q64HZ8 →
Q64I00 0.948 Q64I00 →
Q8W493 0.948 Q8W493 →
Q62950 0.948 Q62950 →
Q6ZFJ3 0.947 Q6ZFJ3 →
Q64I01 0.947 Q64I01 →
P0CB90 0.947 P0CB90 →
C5D9S7 0.947 C5D9S7 →
P00455 0.947 P00455 →
Q62952 0.947 Q62952 →
Q9FQ11 0.946 Q9FQ11 →
Q814N7 0.946 Q814N7 →
Q5IH13 0.946 Q5IH13 →