SPIN4

Spindlin-4 · Q56A73 · SPIN4 on Sugi Atlas →

77 patent compounds predicted against SPIN4, 59 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL29369030 SCHEMBL29369030 1.00 1/20
SCHEMBL19385205 SCHEMBL19385205 0.58 1/20
SCHEMBL29937017 SCHEMBL29937017 0.58 1/20
SCHEMBL2953260 SCHEMBL2953260 0.56 1/20
SCHEMBL28894304 SCHEMBL28894304 0.55 1/20
SCHEMBL19385373 SCHEMBL19385373 0.55 1/20
SCHEMBL1089104 SCHEMBL1089104 0.55 1/20
SCHEMBL1089641 SCHEMBL1089641 0.54 1/20
SCHEMBL1089644 SCHEMBL1089644 0.54 1/20
SCHEMBL1090089 SCHEMBL1090089 0.54 1/20
SCHEMBL19385129 SCHEMBL19385129 0.53 1/20
SCHEMBL25244226 SCHEMBL25244226 0.53 1/20
SCHEMBL28894334 SCHEMBL28894334 0.53 1/20
SCHEMBL19385236 SCHEMBL19385236 0.52 1/20
SCHEMBL19385261 SCHEMBL19385261 0.52 1/20
SCHEMBL19405236 SCHEMBL19405236 0.52 1/20
SCHEMBL25202485 SCHEMBL25202485 0.52 1/20
SCHEMBL19385009 SCHEMBL19385009 0.52 1/20
SCHEMBL23015382 SCHEMBL23015382 0.51 1/20
SCHEMBL19385024 SCHEMBL19385024 0.51 1/20

Clinical trials — most relevant to SPIN4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Phase I Study of SC-43 Oral Solution in Subjects With Refractory Solid Tumors PHASE1WITHDRAWN
Hemolysis in Patients With Hereditary Spherocytosis (HS) nanUNKNOWN
Risk of Ovarian Cancer in Patients With a Pelvic Mass nanCOMPLETED
Study of Synapsis and Recombination in Male Meiosis and the Implications in Infertility nanCOMPLETED
Circulating Cell-free DNA-based Epigenetic Biomarker mSEPT9 for Hepatocellular Carcinoma Detection in Cirrhosis nanCOMPLETED
Efficacy of Cognitive Rehabilitation Using Virtual Reality and Computer-based Cognitive Stimulation on Cognitive Impairment Associated to Movement Disorders nanCOMPLETED
Genetic Investigation of Solid Tumors Cohort nanCOMPLETED
New Genes in the Carcinogenesis of Colorectal Cancer nanUNKNOWN
Consequences of Mutations in the SPG7 Gene at the Heterozygous State nanCOMPLETED
Clinical Manifestations and Biomarkers in Amyotrophic Lateral Sclerosis Type 4 and Other Inherited Neurological Disorders of RNA Processing nanRECRUITING
DNA Analysis in Samples From Younger Patients With Germ Cell Tumors and Their Parents or Siblings nanCOMPLETED
A Positional Cloning Study on Schizophrenia nanCOMPLETED
Adrenal& Bone Complications in Paediatric Patients Living With Spinal Muscular Atrophy (SMA) nanNOT_YET_RECRUITING
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Endolymphatic Sac Tumors in a Population of Patients With Von Hippel-Lindau Disease:The Natural History and Pathobiology, and a Prospective Non-Randomized Clinical Trial of Hearing Preservation Surgery in Patients With Early Stage Endolymphatic Sac Tumors nanCOMPLETED
A Clinical Study on the Safety and Efficacy of CAR-T Therapy for the TM4SF1- and EpCAM-positive Solid Tumors nanUNKNOWN
Implementation of FEES in Spinal Muscle Atrophy nanCOMPLETED
Mechanisms of Cell Death in Spinal Muscular Atrophy nanCOMPLETED
Analysis of Post-Translational Modifications of a Critical Protein Implicated in Amyotrophic Lateral Sclerosis nanCOMPLETED
The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2 nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Improving Genetic Counseling for Patients With Spina Bifida Using Next Generation Sequencing nanCOMPLETED
The Role of HE4 in the Follow-up of Advanced Ovarian, Fallopian Tube and Primary Peritoneal Cancer nanUNKNOWN
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mutations nanUNKNOWN
VRehab-SMA Phase 1.2 nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a SPIN4 binder may also engage these)

ProteinNameSimilarity
Q8K1L2 1.000 Q8K1L2 →
Q6NVE3 0.989 Q6NVE3 →
Q2KI39 0.986 Q2KI39 →
P13675 0.975 P13675 →
Q6YVY0 0.970 Q6YVY0 →
Q32N90 0.969 Q32N90 →
Q6DIN3 0.968 Q6DIN3 →
Q9ZPY6 0.966 Q9ZPY6 →
Q9XED8 0.966 Q9XED8 →
Q9C516 0.966 Q9C516 →
MBTD1 MBT domain-containing protein 1 0.965 landscape →
Q9XID4 0.963 Q9XID4 →
Q8L7G0 0.963 Q8L7G0 →
Q9LQE3 0.963 Q9LQE3 →
P59178 0.960 P59178 →
Q9FWS6 0.960 Q9FWS6 →
Q9C5W9 0.960 Q9C5W9 →
Q5R737 0.960 Q5R737 →
C0SUW7 0.960 C0SUW7 →
O80462 0.960 O80462 →
Q5DTW2 0.960 Q5DTW2 →
Q93VH2 0.959 Q93VH2 →
Q3MIF2 0.959 Q3MIF2 →
Q9BXT6 0.959 Q9BXT6 →
P0C7Q8 0.958 P0C7Q8 →
MAP3K5 Mitogen-activated protein kinase kinase kinase 5 0.958 landscape →
Q8W4F0 0.958 Q8W4F0 →
Q9SFW8 0.958 Q9SFW8 →
Q5JK20 0.958 Q5JK20 →
Q8NE18 0.958 Q8NE18 →