Claudin-9 (CLDN9)

Homo sapiens — UniProt O95484

Gene: CLDN9Homo sapiensSwissProt reviewed

About Claudin-9

Claudin-9 (CLDN9) is a protein from Homo sapiens identified by UniProt accession O95484, 217 residues long. MolForge cross-references it against 0 known binders and 55 disease associations.

Target properties

Protein nameClaudin-9
UniProt accessionO95484
GeneCLDN9
OrganismHomo sapiens
Length217 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 (55)

Diseases linked to this target (Open Targets).

  • hearing loss, autosomal recessive 116 · score 0.62
  • hearing loss · score 0.27
  • endometrial cancer · score 0.23
  • glioblastoma multiforme · score 0.16
  • head and neck squamous cell carcinoma · score 0.15
  • Hearing impairment · score 0.12
  • Pendred syndrome · score 0.12
  • nonsyndromic genetic hearing loss · score 0.12
  • autosomal dominant nonsyndromic hearing loss · score 0.12
  • gastric adenocarcinoma · score 0.09

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O95484-F1alphafoldPREDICTED81.16—

Amino-acid sequence (217 residues)

MASTGLELLG MTLAVLGWLG TLVSCALPLW KVTAFIGNSI VVAQVVWEGL WMSCVVQSTG QMQCKVYDSL LALPQDLQAA RALCVIALLL ALLGLLVAIT GAQCTTCVED EGAKARIVLT AGVILLLAGI LVLIPVCWTA HAIIQDFYNP LVAEALKREL GASLYLGWAA AALLMLGGGL LCCTCPPPQV ERPRGPRLGY SIPSRSGASG LDKRDYV

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Quick facts

UniProtO95484
GeneCLDN9
OrganismHomo sapiens
Length217
Binders0
Diseases55
View on UniProt