Protein FAM167B (FAM167B)

Homo sapiens — UniProt Q9BTA0

Gene: FAM167BHomo sapiensSwissProt reviewed

About Protein FAM167B

Protein FAM167B (FAM167B) is a protein from Homo sapiens identified by UniProt accession Q9BTA0, 163 residues long. MolForge cross-references it against 0 known binders and 9 disease associations.

Target properties

Protein nameProtein FAM167B
UniProt accessionQ9BTA0
GeneFAM167B
OrganismHomo sapiens
Length163 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).

  • neurodegenerative disease · score 0.29
  • lymphocyte count · score 0.03
  • multiple sclerosis · score 0.02
  • Tetralogy of Fallot · score 0.02
  • autism · score 0.01
  • chronic interstitial cystitis · score 0.01
  • ulcerative colitis · score 0.00
  • Crohn's disease · score 0.00
  • Huntington disease · score 0.00

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9BTA0-F1alphafoldPREDICTED75.79—

Amino-acid sequence (163 residues)

MSLGLLKFQA VGEEDEEDEE GESLDSVKAL TAKLQLQTRR PSYLEWTAQV QSQAWRRAQA KPGPGGPGDI CGFDSMDSAL EWLRRELREM QAQDRQLAGQ LLRLRAQLHR LKMDQACHLH QELLDEAELE LELEPGAGLA LAPLLRHLGL TRMNISARRF TLC

Explore Protein FAM167B with MolForge

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Quick facts

UniProtQ9BTA0
GeneFAM167B
OrganismHomo sapiens
Length163
Binders0
Diseases9
View on UniProt