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Transmembrane protein 231 (TMEM231)

Homo sapiens — UniProt Q9H6L2

Gene: TMEM231Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Transmembrane protein 231 (TMEM231) is a protein from Homo sapiens identified by UniProt accession Q9H6L2, 316 residues long. MolForge cross-references it against 0 known binders and 52 disease associations.

  • UniProt accession: Q9H6L2; gene symbol TMEM231.
  • Organism: Homo sapiens.
  • Length: 316 amino acids.
  • Top disease associations (Open Targets): Joubert syndrome with ocular defect, Meckel syndrome and Joubert syndrome with oculorenal defect.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTransmembrane protein 231
UniProt accessionQ9H6L2
GeneTMEM231
OrganismHomo sapiens
Length316 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 (52)

Diseases linked to this target (Open Targets).

  • Joubert syndrome with ocular defect · score 0.75
  • Meckel syndrome · score 0.73
  • Joubert syndrome with oculorenal defect · score 0.62
  • Joubert syndrome and related disorders · score 0.52
  • ciliopathy · score 0.49
  • orofaciodigital syndrome type 6 · score 0.37
  • Orofaciodigital syndrome type 3 · score 0.34
  • genetic disorder · score 0.34
  • congenital hydronephrosis · score 0.26
  • congenital anomaly of kidney and urinary tract · score 0.26

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H6L2-F1alphafoldPREDICTED88.42—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H6L2.

Amino-acid sequence (316 residues)

MALYELFSHP VERSYRAGLC SKAALFLLLA AALTYIPPLL VAFRSHGFWL KRSSYEEQPT VRFQHQVLLV ALLGPESDGF LAWSTFPAFN RLQGDRLRVP LVSTREEDRN QDGKTDMLHF KLELPLQSTE HVLGVQLILT FSYRLHRMAT LVMQSMAFLQ SSFPVPGSQL YVNGDLRLQQ KQPLSCGGLD ARYNISVING TSPFAYDYDL THIVAAYQER NVTTVLNDPN PIWLVGRAAD APFVINAIIR YPVEVISYQP GFWEMVKFAW VQYVSILLIF LWVFERIKIF VFQNQVVTTI PVTVTPRGDL CKEHLS

Frequently asked questions

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

Which diseases are associated with TMEM231?

The strongest Open Targets associations for TMEM231 are Joubert syndrome with ocular defect, Meckel syndrome, Joubert syndrome with oculorenal defect, Joubert syndrome and related disorders and ciliopathy.

How long is the TMEM231 protein?

The Homo sapiens TMEM231 protein (UniProt Q9H6L2) is 316 amino acids long.

Browse: Targets: T · 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.

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Quick facts

UniProtQ9H6L2
GeneTMEM231
OrganismHomo sapiens
Length316
Binders0
Diseases52
View on UniProt