Sugi Predict

Sugi Predict / Targets / NHP2

NHP2

H/ACA ribonucleoprotein complex subunit 2 · Q9NX24 · NHP2 on Sugi Atlas →

0 patent compounds predicted against NHP2, 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 NHP2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Study of Specimens From Young Patients With Neuroblastoma nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
LINC00511/miR-185-3p Axis and miR-301a-3p Markers for Breast Cancer Diagnosis nanCOMPLETED
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
CABP2 Patient Registry and Natural History Study nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Microarray Analysis in Syndromic Obesity nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a NHP2 binder may also engage these)

ProteinNameSimilarity
Q5RC65 — 1.000 Q5RC65 →
Q5E950 — 1.000 Q5E950 →
Q9CRB2 — 0.988 Q9CRB2 →
Q6P8C4 — 0.964 Q6P8C4 →
Q6PBV6 — 0.962 Q6PBV6 →
Q6NTV9 — 0.961 Q6NTV9 →
Q9U3Z7 — 0.933 Q9U3Z7 →
Q9Z1F9 — 0.933 Q9Z1F9 →
Q4P0K3 — 0.932 Q4P0K3 →
Q9JHW4 — 0.932 Q9JHW4 →
Q13868 — 0.932 Q13868 →
Q2KID0 — 0.932 Q2KID0 →
Q3KRC5 — 0.931 Q3KRC5 →
Q5ZJH9 — 0.930 Q5ZJH9 →
Q9ESX5 — 0.930 Q9ESX5 →
Q2KIX1 — 0.930 Q2KIX1 →
D2XV59 — 0.930 D2XV59 →
Q21568 — 0.929 Q21568 →
Q7ZWS1 — 0.929 Q7ZWS1 →
Q811P6 — 0.929 Q811P6 →
GLS2 Glutaminase liver isoform, mitochondrial 0.929 landscape →
Q5XGS8 — 0.928 Q5XGS8 →
Q6UPE1 — 0.928 Q6UPE1 →
Q9XS70 — 0.928 Q9XS70 →
Q8VBV3 — 0.928 Q8VBV3 →
TPP2 Tripeptidyl-peptidase 2 0.928 landscape →
Q6BLQ3 — 0.928 Q6BLQ3 →
P80314 — 0.928 P80314 →
Q3ZBH0 — 0.928 Q3ZBH0 →
Q9SIZ2 — 0.928 Q9SIZ2 →