Skip to content

WW domain-containing oxidoreductase (WWOX)

Homo sapiens — UniProt Q9NZC7

Gene: WWOXHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

WW domain-containing oxidoreductase (WWOX) is a protein from Homo sapiens identified by UniProt accession Q9NZC7, 414 residues long. MolForge cross-references it against 0 known binders and 542 disease associations.

  • UniProt accession: Q9NZC7; gene symbol WWOX.
  • Organism: Homo sapiens.
  • Length: 414 amino acids.
  • Top disease associations (Open Targets): autosomal recessive spinocerebellar ataxia 12, developmental and epileptic encephalopathy, 28 and developmental and epileptic encephalopathy.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameWW domain-containing oxidoreductase
UniProt accessionQ9NZC7
GeneWWOX
OrganismHomo sapiens
Length414 residues
Molecular weight—
EC numbers—
Target class—
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 (542)

Diseases linked to this target (Open Targets).

  • autosomal recessive spinocerebellar ataxia 12 · score 0.80
  • developmental and epileptic encephalopathy, 28 · score 0.76
  • developmental and epileptic encephalopathy · score 0.67
  • undetermined early-onset epileptic encephalopathy · score 0.66
  • esophageal squamous cell carcinoma · score 0.64
  • West syndrome · score 0.55
  • developmental and epileptic encephalopathy, 1 · score 0.55
  • infantile epileptic-dyskinetic encephalopathy · score 0.55
  • Spasticity - intellectual disability - X-linked epilepsy · score 0.55
  • vital capacity · score 0.50

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NZC7-F1alphafoldPREDICTED85.60—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NZC7.

Amino-acid sequence (414 residues)

MAALRYAGLD DTDSEDELPP GWEERTTKDG WVYYANHTEE KTQWEHPKTG KRKRVAGDLP YGWEQETDEN GQVFFVDHIN KRTTYLDPRL AFTVDDNPTK PTTRQRYDGS TTAMEILQGR DFTGKVVVVT GANSGIGFET AKSFALHGAH VILACRNMAR ASEAVSRILE EWHKAKVEAM TLDLALLRSV QHFAEAFKAK NVPLHVLVCN AATFALPWSL TKDGLETTFQ VNHLGHFYLV QLLQDVLCRS APARVIVVSS ESHRFTDIND SLGKLDFSRL SPTKNDYWAM LAYNRSKLCN ILFSNELHRR LSPRGVTSNA VHPGNMMYSN IHRSWWVYTL LFTLARPFTK SMQQGAATTV YCAAVPELEG LGGMYFNNCC RCMPSPEAQS EETARTLWAL SERLIQERLG SQSG

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with WWOX?

The strongest Open Targets associations for WWOX are autosomal recessive spinocerebellar ataxia 12, developmental and epileptic encephalopathy, 28, developmental and epileptic encephalopathy, undetermined early-onset epileptic encephalopathy and esophageal squamous cell carcinoma.

How long is the WWOX protein?

The Homo sapiens WWOX protein (UniProt Q9NZC7) is 414 amino acids long.

Browse: Targets: W · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Explore WW domain-containing oxidoreductase 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

UniProtQ9NZC7
GeneWWOX
OrganismHomo sapiens
Length414
Binders0
Diseases542
View on UniProt