FLYWCH family member 2 (FLYWCH2)

Homo sapiens — UniProt Q96CP2

Gene: FLYWCH2Homo sapiensSwissProt reviewed

About FLYWCH family member 2

FLYWCH family member 2 (FLYWCH2) is a protein from Homo sapiens identified by UniProt accession Q96CP2, 140 residues long. MolForge cross-references it against 0 known binders and 53 disease associations.

Target properties

Protein nameFLYWCH family member 2
UniProt accessionQ96CP2
GeneFLYWCH2
OrganismHomo sapiens
Length140 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 (53)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.33
  • Brugada syndrome · score 0.09
  • familial atrial fibrillation · score 0.08
  • Romano-Ward syndrome · score 0.08
  • Familial short QT syndrome · score 0.07
  • Familial progressive cardiac conduction defect · score 0.07
  • Brugada syndrome 9 · score 0.07
  • Arrhythmogenic right ventricular dysplasia · score 0.07
  • familial sick sinus syndrome · score 0.06
  • long QT syndrome 11 · score 0.06

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96CP2-F1alphafoldPREDICTED66.78—

Amino-acid sequence (140 residues)

MPLPEPSEQE GESVKASQEP SPKPGTEVIP AAPRKPRKFS KLVLLTASKD STKVAGAKRK GVHCVMSLGV PGPATLAKAL LQTHPEAQRA IEAAPQEPEQ KRSRQDPGTD RTEDSGLAAG PPEAAGENFA PCSVAPGKSL

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Quick facts

UniProtQ96CP2
GeneFLYWCH2
OrganismHomo sapiens
Length140
Binders0
Diseases53
View on UniProt