Noggin (NOG)

Homo sapiens — UniProt Q13253

Gene: NOGHomo sapiensSwissProt reviewed

About Noggin

Noggin (NOG) is a protein from Homo sapiens identified by UniProt accession Q13253, 232 residues long. MolForge cross-references it against 0 known binders and 382 disease associations.

Target properties

Protein nameNoggin
UniProt accessionQ13253
GeneNOG
OrganismHomo sapiens
Length232 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 (382)

Diseases linked to this target (Open Targets).

  • proximal symphalangism 1A · score 0.79
  • tarsal-carpal coalition syndrome · score 0.75
  • brachydactyly type B2 · score 0.74
  • multiple synostoses syndrome 1 · score 0.73
  • stapes ankylosis with broad thumbs and toes · score 0.71
  • multiple synostoses syndrome · score 0.61
  • genetic disorder · score 0.47
  • refractive error measurement · score 0.42
  • body height · score 0.41
  • cleft lip · score 0.40

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q13253-F1alphafoldPREDICTED86.08—

Amino-acid sequence (232 residues)

MERCPSLGVT LYALVVVLGL RATPAGGQHY LHIRPAPSDN LPLVDLIEHP DPIFDPKEKD LNETLLRSLL GGHYDPGFMA TSPPEDRPGG GGGAAGGAED LAELDQLLRQ RPSGAMPSEI KGLEFSEGLA QGKKQRLSKK LRRKLQMWLW SQTFCPVLYA WNDLGSRFWP RYVKVGSCFS KRSCSVPEGM VCKPSKSVHL TVLRWRCQRR GGQRCGWIPI QYPIISECKC SC

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Quick facts

UniProtQ13253
GeneNOG
OrganismHomo sapiens
Length232
Binders0
Diseases382
View on UniProt