Targets — browse / sort / filter (view)

One row per human protein target with names + key evidence. Click column headers to SORT; use the facets to FILTER (tier, activation pair, known aptamer, EV-Map). UniProt IDs link to the source.

Data license: CC BY 4.0 · Data source: apt-scout automated curation pipeline (E. Dohi, NCNP) — values harvested from public databases; raw source stored per target

id
UniProt accession (human). Links to uniprot.org.
gene_symbol
Gene symbol (e.g. ITGB3).
protein_name
Protein name (UniProt).
tier
Tier 1 = PDB-anchored; Tier 1.5 = AlphaFold-confident.
priority_score
Composite prioritisation = 0.30*biology + 0.30*reagent-gap + 0.20*druggability + 0.10*disease + 0.10*novelty. Sub-scores are assigned during LLM-assisted curation — a heuristic ranking, NOT an experimental measurement.
has_activation_state_pdb_pair
1 if a curated ACTIVE/INACTIVE PDB pair exists (only 11 targets).
in_cev_map
1 if in the EV-Map circulating-EV proteome (Rai 2025); 3,422 targets.
has_known_aptamer
1 if aptamer evidence found in PubMed/Aptagen (1,472 targets).
opentargets_top_disease_score
Open Targets association score (0-1).
aptamer_count_pubmed
Number of PubMed hits for this protein AND (aptamer OR SELEX).
aptamer_pmids
The actual PubMed IDs behind the aptamer evidence — click each to read the paper. This is the source of the 'has aptamer' claim.

1,299 rows where has_known_aptamer = 0, in_cev_map = 1 and tier = "Tier 1.5" sorted by priority_score descending

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Suggested facets: pdb_count_total

has_cryoEM 2

  • 0 1,112
  • 1 187

tier 1

  • Tier 1.5 · 1,299 ✖

in_cev_map 1

  • 1 · 1,299 ✖

has_known_aptamer 1

  • - · 1,299 ✖

has_activation_state_pdb_pair 1

  • 0 1,299
id gene_symbol protein_name tier priority_score ▲ pdb_count_total alphafold_mean_pLDDT has_cryoEM has_activation_state_pdb_pair activation_state_pdb_active activation_state_pdb_inactive drug_count_approved has_known_aptamer aptamer_count_pubmed aptamer_pmids in_cev_map opentargets_top_disease_name opentargets_top_disease_score
Q9NX14 NDUFB11 NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial Tier 1.5 0.86 0 77.56 0 0       0 0   1 Microphthalmia with linear skin defects syndrome 0.7364493324598024
Q02094 RHAG Ammonium transporter Rh type A Tier 1.5 0.841 8 95.62 1 0       0 0   1 Rh deficiency syndrome 0.764209214915708
Q14392 LRRC32 Transforming growth factor beta activator LRRC32 Tier 1.5 0.838 6 86.06 1 0       0 0   1 cleft palate, proliferative retinopathy, and developmental delay 0.5770707112957068
P12532 CKMT1A Creatine kinase U-type, mitochondrial Tier 1.5 0.83 9 89.31 1 0       0 0   1 neurodegenerative disease 0.5385822922582763
P54709 ATP1B3 Sodium/potassium-transporting ATPase subunit beta-3 Tier 1.5 0.81 7 89.69 1 0       0 0   1 congestive heart failure 0.5999952111132625
Q9UBT7 CTNNAL1 Alpha-catulin Tier 1.5 0.795 0 84.06 0 0       0 0   1 Abnormality of the skeletal system 0.31316995706583495
P27037 ACVR2A Activin receptor type-2A Tier 1.5 0.769 5 83.56 0 0       0 0   1 hepatocellular carcinoma 0.4908023126074436
O14958 CASQ2 Calsequestrin-2 Tier 1.5 0.767 4 90.5 0 0       0 0   1 catecholaminergic polymorphic ventricular tachycardia 0.7718998507471558
Q9H3K6 BOLA2 BolA-like protein 2 Tier 1.5 0.765 0 92.69 0 0       0 0   1 hepatocellular carcinoma 0.08093942543094014
O60568 PLOD3 Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 Tier 1.5 0.762 18 91.38 1 0       0 0   1 bone fragility with contractures, arterial rupture, and deafness 0.7159150369336311
P41440 SLC19A1 Reduced folate transporter Tier 1.5 0.755 19 72.06 1 0       0 0   1 Knobloch syndrome 0.5526223217595396
P26022 PTX3 Pentraxin-related protein PTX3 Tier 1.5 0.75 9 76.75 1 0       0 0   1 polycystic ovary syndrome 0.12287624125782433
Q92956 TNFRSF14 Tumor necrosis factor receptor superfamily member 14 Tier 1.5 0.745 8 79.94 0 0       0 0   1 diffuse large B-cell lymphoma 0.5983171413833771
Q9Y653 ADGRG1 Adhesion G-protein coupled receptor G1 Tier 1.5 0.743 1 77.88 1 0       0 0   1 bilateral frontoparietal polymicrogyria 0.8322298896713178
P16389 KCNA2 Potassium voltage-gated channel subfamily A member 2 Tier 1.5 0.735 0 77.38 0 0       0 0   1 genetic developmental and epileptic encephalopathy 0.7513374591580034
P98196 ATP11A Phospholipid-transporting ATPase IH Tier 1.5 0.735 0 82.94 0 0       0 0   1 hearing loss, autosomal dominant 84 0.5506821963658654
P20702 ITGAX Integrin alpha-X Tier 1.5 0.732 9 88.0 0 0       0 0   1 neurodegenerative disease 0.41708750879240836
P09603     Tier 1.5 0.729 8 57.41 0 0       0 0   1 type 2 diabetes mellitus 0.39219340856589974
P22732 SLC2A5 Solute carrier family 2, facilitated glucose transporter member 5 Tier 1.5 0.728 0 90.56 0 0       0 0   1 Prolonged QT interval 0.3326218692162316
Q9P2B2 PTGFRN Prostaglandin F2 receptor negative regulator Tier 1.5 0.728 0 84.12 0 0       0 0   1 type 2 diabetes mellitus 0.48052208463481294
Q92636 NSMAF Protein FAN Tier 1.5 0.725 0 88.31 0 0       0 0   1 placental retention 0.36802220150078147
P07942 LAMB1 Laminin subunit beta-1 Tier 1.5 0.72 3 76.69 1 0       0 0   1 cobblestone lissencephaly without muscular or ocular involvement 0.8016665947624902
Q9NR82 KCNQ5 Potassium voltage-gated channel subfamily KQT member 5 Tier 1.5 0.711 5 56.41 1 0       0 0   1 intellectual disability, autosomal dominant 46 0.7086662845211597
O95562 SFT2D2 Vesicle transport protein SFT2B Tier 1.5 0.71 0 78.5 0 0       0 0   1 neurodegenerative disease 0.38598268164814226
P79483 HLA-DRB3 HLA class II histocompatibility antigen, DR beta 3 chain Tier 1.5 0.71 2 88.38 0 0       0 0   1    
P03905 MT-ND4 NADH-ubiquinone oxidoreductase chain 4 Tier 1.5 0.705 0 93.94 0 0       0 0   1 Leber hereditary optic neuropathy 0.7517935125709835
P14770 GP9 Platelet glycoprotein IX Tier 1.5 0.702 2 84.69 1 0       0 0   1 Bernard-Soulier syndrome 0.8233582238860002
P01615 IGKV2D-28 Immunoglobulin kappa variable 2D-28 Tier 1.5 0.695 0 91.0 0 0       0 0   1 cutaneous Leishmaniasis 0.5868213846274001
Q30154 HLA-DRB5 HLA class II histocompatibility antigen, DR beta 5 chain Tier 1.5 0.694 4 86.75 0 0       0 0   1 seasonal allergic rhinitis 0.19424611770933498
Q9Y678 COPG1 Coatomer subunit gamma-1 Tier 1.5 0.692 1 87.88 0 0       0 0   1 neurodegenerative disease 0.4905625531390244
P36980 CFHR2 Complement factor H-related protein 2 Tier 1.5 0.691 4 90.62 0 0       0 0   1 age-related macular degeneration 0.5100732932209376
P01825 IGHV4-59 Immunoglobulin heavy variable 4-59 Tier 1.5 0.69 3 91.56 1 0       0 0   1 cutaneous Leishmaniasis 0.5868213846274001
Q8IUH8 SPPL2C Signal peptide peptidase-like 2C Tier 1.5 0.69 0 67.06 0 0       0 0   1 osteoarthritis, hip 0.35379836590273994
Q6NT16 SLC18B1 MFS-type transporter SLC18B1 Tier 1.5 0.688 4 84.62 1 0       0 0   1 Parkinson disease 0.276931649354752
Q14520 HABP2 Factor VII-activating protease Tier 1.5 0.686 0 77.62 0 0       0 0   1 follicular thyroid carcinoma 0.46213907606907034
Q96MP8 KCTD7 BTB/POZ domain-containing protein KCTD7 Tier 1.5 0.685 0 81.12 0 0       0 0   1 progressive myoclonic epilepsy type 3 0.8021556079083692
Q99250 SCN2A Sodium channel protein type 2 subunit alpha Tier 1.5 0.685 5 68.81 1 0       0 0   1 developmental and epileptic encephalopathy, 11 0.8388748085806758
Q15582 TGFBI Transforming growth factor-beta-induced protein ig-h3 Tier 1.5 0.682 10 90.25 1 0       0 0   1 lattice corneal dystrophy type I 0.8242841141270143
O75935 DCTN3 Dynactin subunit 3 Tier 1.5 0.68 1 88.38 1 0       0 0   1 viral disease 0.03700998752471888
Q8TD43 TRPM4 Transient receptor potential cation channel subfamily M member 4 Tier 1.5 0.68 25 77.44 1 0       0 0   1 Familial progressive cardiac conduction defect 0.7868180621357534
O94842 TOX4 TOX high mobility group box family member 4 Tier 1.5 0.68 1 54.72 0 0       0 0   1 neurodegenerative disease 0.43085410155338943
P05023 ATP1A1 Sodium/potassium-transporting ATPase subunit alpha-1 Tier 1.5 0.679 10 88.69 1 0       0 0   1 Charcot-Marie-tooth disease, axonal, type 2DD 0.7868851290226483
Q92536 SLC7A6 Y+L amino acid transporter 2 Tier 1.5 0.678 2 83.19 1 0       0 0   1 Abnormality of the skeletal system 0.48544421359843914
Q96DA2 RAB39B Ras-related protein Rab-39B Tier 1.5 0.678 1 88.38 0 0       0 0   1 early-onset parkinsonism-intellectual disability syndrome 0.7782306319395635
P36021 SLC16A2 Monocarboxylate transporter 8 Tier 1.5 0.675 7 79.56 1 0       0 0   1 Allan-Herndon-Dudley syndrome 0.8533069932022032
P18564 ITGB6 Integrin beta-6 Tier 1.5 0.675 14 82.88 1 0       0 0   1 Hypoplastic amelogenesis imperfecta 0.6045342804405103
Q9UI42 CPA4 Carboxypeptidase A4 Tier 1.5 0.674 5 93.69 0 0       0 0   1 rheumatoid arthritis 0.19026118958920038
P08572 COL4A2 Collagen alpha-2(IV) chain Tier 1.5 0.673 4 47.25 0 0       0 0   1 porencephaly 2 0.7294975109351518
P78357 CNTNAP1 Contactin-associated protein 1 Tier 1.5 0.673 0 81.12 0 0       0 0   1 Hypomyelination neuropathy - arthrogryposis 0.8286745612673082
Q14C86 GAPVD1 GTPase-activating protein and VPS9 domain-containing protein 1 Tier 1.5 0.67 0 62.19 0 0       0 0   1 Abnormality of the skeletal system 0.46694942126454214

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CREATE VIEW v_targets AS
SELECT f.id, n.gene_symbol, n.protein_name, tg.tier, f.priority_score,
 f.pdb_count_total, f.alphafold_mean_pLDDT, f.has_cryoEM,
 f.has_activation_state_pdb_pair, f.activation_state_pdb_active, f.activation_state_pdb_inactive,
 f.drug_count_approved, f.has_known_aptamer, f.aptamer_count_pubmed, ap.aptamer_pmids,
 f.in_cev_map, f.opentargets_top_disease_name, f.opentargets_top_disease_score
FROM v_target_full f
LEFT JOIN target_names n ON n.target_id=f.id
LEFT JOIN targets tg ON tg.id=f.id
LEFT JOIN target_aptamer_pmids ap ON ap.target_id=f.id;