Protein C19orf12 (C19orf12)

Homo sapiens — UniProt Q9NSK7

Gene: C19orf12Homo sapiensSwissProt reviewed

About Protein C19orf12

Protein C19orf12 (C19orf12) is a protein from Homo sapiens identified by UniProt accession Q9NSK7, 141 residues long. MolForge cross-references it against 0 known binders and 80 disease associations.

Target properties

Protein nameProtein C19orf12
UniProt accessionQ9NSK7
GeneC19orf12
OrganismHomo sapiens
Length141 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 (80)

Diseases linked to this target (Open Targets).

  • neurodegeneration with brain iron accumulation 4 · score 0.85
  • hereditary spastic paraplegia 43 · score 0.69
  • Autosomal recessive spastic paraplegia type 43 · score 0.69
  • neurodegeneration with brain iron accumulation · score 0.51
  • hereditary spastic paraplegia · score 0.46
  • Mental deterioration · score 0.34
  • Dystonia · score 0.34
  • dystonic disorder · score 0.34
  • Tremor · score 0.34
  • essential tremor · score 0.34

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NSK7-F1alphafoldPREDICTED60.06—

Amino-acid sequence (141 residues)

MTIMVEDIMK LLCSLSGERK MKAAVKHSGK GALVTGAMAF VGGLVGGPPG LAVGGAVGGL LGAWMTSGQF KPVPQILMEL PPAEQQRLFN EAAAIIRHLE WTDAVQLTAL VMGSEALQQQ LLAMLVNYVT KELRAEIQYD D

Explore Protein C19orf12 with MolForge

Find binders, run structure-based screening, and map this target across diseases and approved drugs with our AI-powered platform.

Browse all targets

Quick facts

UniProtQ9NSK7
GeneC19orf12
OrganismHomo sapiens
Length141
Binders0
Diseases80
View on UniProt