Syncollin (SYCN)

Homo sapiens — UniProt Q0VAF6

Gene: SYCNHomo sapiensSwissProt reviewed

About Syncollin

Syncollin (SYCN) is a protein from Homo sapiens identified by UniProt accession Q0VAF6, 134 residues long. MolForge cross-references it against 0 known binders and 20 disease associations.

Target properties

Protein nameSyncollin
UniProt accessionQ0VAF6
GeneSYCN
OrganismHomo sapiens
Length134 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (20)

Diseases linked to this target (Open Targets).

  • Hyperlipoproteinemia type 1 · score 0.06
  • chronic pancreatitis · score 0.05
  • hereditary chronic pancreatitis · score 0.04
  • bronchiectasis with or without elevated sweat chloride 1 · score 0.04
  • Bronchiectasis · score 0.04
  • GCGR-related hyperglucagonemia · score 0.04
  • hyperinsulinemic hypoglycemia, familial, 2 · score 0.04
  • gallbladder disease · score 0.03
  • pancreatic agenesis 2 · score 0.03
  • benign recurrent intrahepatic cholestasis type 1 · score 0.03

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q0VAF6-F1alphafoldPREDICTED87.73—

Amino-acid sequence (134 residues)

MSPLRPLLLA LALASVPCAQ GACPASADLK HSDGTRTCAK LYDKSDPYYE NCCGGAELSL ESGADLPYLP SNWANTASSL VVAPRCELTV WSRQGKAGKT HKFSAGTYPR LEEYRRGILG DWSNAISALY CRCS

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Quick facts

UniProtQ0VAF6
GeneSYCN
OrganismHomo sapiens
Length134
Binders0
Diseases20
View on UniProt