Protein FAM98C (FAM98C)

Homo sapiens — UniProt Q17RN3

Gene: FAM98CHomo sapiensSwissProt reviewed

About Protein FAM98C

Protein FAM98C (FAM98C) is a protein from Homo sapiens identified by UniProt accession Q17RN3, 349 residues long. MolForge cross-references it against 0 known binders and 9 disease associations.

Target properties

Protein nameProtein FAM98C
UniProt accessionQ17RN3
GeneFAM98C
OrganismHomo sapiens
Length349 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 (9)

Diseases linked to this target (Open Targets).

  • autism spectrum disorder · score 0.26
  • asphyxiating thoracic dystrophy 3 · score 0.26
  • short rib-polydactyly syndrome, Majewski type · score 0.26
  • Short rib-polydactyly syndrome, Verma-Naumoff type · score 0.26
  • eosinophil count · score 0.06
  • D dimer measurement · score 0.05
  • eosinophil percentage of leukocytes · score 0.04
  • basophil count · score 0.03
  • neutrophil percentage of granulocytes · score 0.03

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q17RN3-F1alphafoldPREDICTED79.20—

Amino-acid sequence (349 residues)

MEAVKAEAWE GAAVAQDLLA LGYGGVPGAA SRGASCPDFR GLCVRLAAEL ATLGALEQQR EAGAEVLSAG DGPGAEEDFL RQLGSLLREL HCPDRALCGG DGAAALREPG AGLRLLRFLC SELQATRLLC LRSLLDPSPR PPLGEGVVEG AGMVQELDLT LQALGLPRPA PGTPASQLLQ ELHAKISELQ PSLPPGSLQP LLSCSLDAPR WEALESLSQS LRDQYRCRRC LLLKRLDLTT SAFHWSDRAE AQGEAMRAVL IPIREVLTPE SDISIAHVLA ARADLSCLVP ATSVAVRRGT CCAINKVLMG NVPDRGGRPN ELEPPMPTWR SRREDGGPQC WGRKKKKKK

Explore Protein FAM98C with MolForge

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Quick facts

UniProtQ17RN3
GeneFAM98C
OrganismHomo sapiens
Length349
Binders0
Diseases9
View on UniProt