Fascin-2 (FSCN2)

Homo sapiens — UniProt O14926

Gene: FSCN2Homo sapiensSwissProt reviewed

About Fascin-2

Fascin-2 (FSCN2) is a protein from Homo sapiens identified by UniProt accession O14926, 492 residues long. MolForge cross-references it against 0 known binders and 134 disease associations.

Target properties

Protein nameFascin-2
UniProt accessionO14926
GeneFSCN2
OrganismHomo sapiens
Length492 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 (134)

Diseases linked to this target (Open Targets).

  • retinitis pigmentosa · score 0.49
  • Retinal dystrophy · score 0.39
  • macular degeneration · score 0.33
  • hearing loss · score 0.26
  • age-related hearing impairment · score 0.22
  • serum gamma-glutamyl transferase measurement · score 0.18
  • Meniere disease · score 0.16
  • Leber congenital amaurosis · score 0.13
  • aspartate aminotransferase to alanine aminotransferase ratio · score 0.09
  • sex hormone-binding globulin measurement · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O14926-F1alphafoldPREDICTED93.63—

Amino-acid sequence (492 residues)

MPTNGLHQVL KIQFGLVNDT DRYLTAESFG FKVNASAPSL KRKQTWVLEP DPGQGTAVLL RSSHLGRYLS AEEDGRVACE AEQPGRDCRF LVLPQPDGRW VLRSEPHGRF FGGTEDQLSC FATAVSPAEL WTVHLAIHPQ AHLLSVSRRR YVHLCPREDE MAADGDKPWG VDALLTLIFR SRRYCLKSCD SRYLRSDGRL VWEPEPRACY TLEFKAGKLA FKDCDGHYLA PVGPAGTLKA GRNTRPGKDE LFDLEESHPQ VVLVAANHRY VSVRQGVNVS ANQDDELDHE TFLMQIDQET KKCTFYSSTG GYWTLVTHGG IHATATQVSA NTMFEMEWRG RRVALKASNG RYVCMKKNGQ LAAISDFVGK DEEFTLKLIN RPILVLRGLD GFVCHHRGSN QLDTNRSVYD VFHLSFSDGA YRIRGRDGGF WYTGSHGSVC SDGERAEDFV FEFRERGRLA IRARSGKYLR GGASGLLRAD ADAPAGTALW EY

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Quick facts

UniProtO14926
GeneFSCN2
OrganismHomo sapiens
Length492
Binders0
Diseases134
View on UniProt