Neurogranin (NRGN)

Homo sapiens — UniProt Q92686

Gene: NRGNHomo sapiensSwissProt reviewed

About Neurogranin

Neurogranin (NRGN) is a protein from Homo sapiens identified by UniProt accession Q92686, 78 residues long. MolForge cross-references it against 0 known binders and 209 disease associations.

Target properties

Protein nameNeurogranin
UniProt accessionQ92686
GeneNRGN
OrganismHomo sapiens
Length78 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 (209)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.44
  • schizophrenia · score 0.30
  • autism spectrum disorder · score 0.22
  • attention deficit hyperactivity disorder · score 0.22
  • bipolar disorder · score 0.18
  • unipolar depression · score 0.18
  • obsessive-compulsive disorder · score 0.18
  • anorexia nervosa · score 0.18
  • Tourette syndrome · score 0.18
  • intelligence · score 0.18

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q92686-F1alphafoldPREDICTED68.14—

Amino-acid sequence (78 residues)

MDCCTENACS KPDDDILDIP LDDPGANAAA AKIQASFRGH MARKKIKSGE RGRKGPGPGG PGGAGVARGG AGGGPSGD

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Quick facts

UniProtQ92686
GeneNRGN
OrganismHomo sapiens
Length78
Binders0
Diseases209
View on UniProt