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CALML3

Calmodulin-like protein 3 · P27482 · CALML3 on Sugi Atlas →

24,984 patent compounds predicted against CALML3, 16,947 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL542030 SCHEMBL542030 0.67 7/20
SCHEMBL542031 SCHEMBL542031 0.67 7/20
SCHEMBL1222787 SCHEMBL1222787 0.67 7/20
SCHEMBL1222791 SCHEMBL1222791 0.67 7/20
SCHEMBL412800 SCHEMBL412800 0.65 7/20
SCHEMBL441045 SCHEMBL441045 0.65 7/20
SCHEMBL1035579 SCHEMBL1035579 0.65 7/20
SCHEMBL1393956 SCHEMBL1393956 0.63 7/20
SCHEMBL1393478 SCHEMBL1393478 0.61 7/20
SCHEMBL1394150 SCHEMBL1394150 0.61 7/20
SCHEMBL1393511 SCHEMBL1393511 0.59 7/20
SCHEMBL1393695 SCHEMBL1393695 0.59 7/20
SCHEMBL1393834 SCHEMBL1393834 0.59 7/20
SCHEMBL1393466 SCHEMBL1393466 0.57 7/20
SCHEMBL1393474 SCHEMBL1393474 0.57 7/20
SCHEMBL1393590 SCHEMBL1393590 0.56 7/20
SCHEMBL1393703 SCHEMBL1393703 0.56 7/20
SCHEMBL1393819 SCHEMBL1393819 0.56 7/20
SCHEMBL411137 SCHEMBL411137 0.56 7/20
SCHEMBL1393621 SCHEMBL1393621 0.56 7/20

Clinical trials — most relevant to CALML3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Relationship of Gestational Age and Urine Concentration of S100B in Preterm and Term Infants in the First Week of Life nanCOMPLETED
Multicenter Study of Patients With SHANK3 Mutations: Identification of Genes Modificators in Phelan-McDermid Syndrome (EUQ13) nanNOT_YET_RECRUITING
The Prevalence of RYR1-related Disease nanNOT_YET_RECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Comparison of Two Methods to Diagnose Coronary Artery Disease nanCOMPLETED
Calmodulin Gene Mutations in Patients With Ventricular Arrhythmia of Unknown Origin - A Screening Study nanWITHDRAWN
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia nanCOMPLETED
Identification of Novel Molecular Markers for Vasospasm nanCOMPLETED
Inflammatory Genomics in Human Carotid Artery Disease nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
A Natural History Study of RYR1-Related Disorders nanRECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Clinical and Genetic Study of Autism Spectrum Disorder nanCOMPLETED
Proteomics to Identify Prognostic Markers After CPR and to Estimate Neurological Outcome nanCOMPLETED
Characterization of Patients With Cardiomyopathy to Identify Critical Patients Candidates for Cardiac Transplantation nanRECRUITING
Determining the Association of Chromosomal Variants With Non-PV Triggers and Ablation-outcome in AF (DECAF) nanCOMPLETED
IP3R Modulation by Cancer Genes in Mesothelioma nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Evaluation of Vasopressin in the Vessels of Ovarian Neoplasms nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Genomic Study of Congenital Malformation nanUNKNOWN
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Blood-based Biomarkers for the Prognosis of Sports Related Concussion nanCOMPLETED
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Genetic Markers of CHD Risk in Men and Women nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CALML3 binder may also engage these)

ProteinNameSimilarity
P02597 — 0.999 P02597 →
P07463 — 0.996 P07463 →
P61861 — 0.996 P61861 →
Q9D6P8 — 0.995 Q9D6P8 →
Q5U206 — 0.995 Q5U206 →
Q9UB37 — 0.995 Q9UB37 →
Q9U6D3 — 0.995 Q9U6D3 →
P05933 — 0.995 P05933 →
P62202 — 0.994 P62202 →
P27163 — 0.994 P27163 →
Q9UWF0 — 0.994 Q9UWF0 →
P61859 — 0.994 P61859 →
Q7DMN9 — 0.994 Q7DMN9 →
P60206 — 0.993 P60206 →
Q39752 — 0.993 Q39752 →
P41041 — 0.993 P41041 →
P62201 — 0.993 P62201 →
P62156 — 0.993 P62156 →
P62144 — 0.993 P62144 →
Q6YNX6 — 0.993 Q6YNX6 →
P0DP25 — 0.993 P0DP25 →
P0DP33 — 0.993 P0DP33 →
P0DP28 — 0.993 P0DP28 →
P04353 — 0.993 P04353 →
P62200 — 0.992 P62200 →
P60205 — 0.992 P60205 →
P60204 — 0.992 P60204 →
Q0JNL7 — 0.992 Q0JNL7 →
P61860 — 0.992 P61860 →
P0DH97 — 0.992 P0DH97 →