Oncomodulin-2 (OCM2)

Homo sapiens — UniProt P0CE71

Gene: OCM2Homo sapiensSwissProt reviewed

About Oncomodulin-2

Oncomodulin-2 (OCM2) is a protein from Homo sapiens identified by UniProt accession P0CE71, 109 residues long. MolForge cross-references it against 0 known binders and 37 disease associations.

Target properties

Protein nameOncomodulin-2
UniProt accessionP0CE71
GeneOCM2
OrganismHomo sapiens
Length109 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 (37)

Diseases linked to this target (Open Targets).

  • deafness · score 0.11
  • hearing loss, autosomal recessive · score 0.09
  • autosomal dominant nonsyndromic hearing loss 7 · score 0.07
  • autosomal dominant nonsyndromic hearing loss 17 · score 0.07
  • deafness, aminoglycoside-induced · score 0.07
  • autosomal dominant nonsyndromic hearing loss · score 0.07
  • autosomal recessive nonsyndromic hearing loss 1B · score 0.07
  • Non-syndromic genetic deafness · score 0.07
  • Meniere disease · score 0.07
  • otosclerosis · score 0.07

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P0CE71-F1alphafoldPREDICTED91.53—

Amino-acid sequence (109 residues)

MSITDVLSAD DIAAALQECQ DPDTFEPQKF FQTSGLSKMS ASQVKDVFRF IDNDQSGYLD EEELKFFLQK FESGARELTE SETKSLMAAA DNDGDGKIGA EEFQEMVHS

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Quick facts

UniProtP0CE71
GeneOCM2
OrganismHomo sapiens
Length109
Binders0
Diseases37
View on UniProt