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Transmembrane protein 216 (TMEM216)

Homo sapiens — UniProt Q9P0N5

Gene: TMEM216Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Transmembrane protein 216 (TMEM216) is a protein from Homo sapiens identified by UniProt accession Q9P0N5, 145 residues long. MolForge cross-references it against 0 known binders and 72 disease associations.

  • UniProt accession: Q9P0N5; gene symbol TMEM216.
  • Organism: Homo sapiens.
  • Length: 145 amino acids.
  • Top disease associations (Open Targets): Joubert syndrome, Meckel syndrome and Joubert syndrome with oculorenal defect.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTransmembrane protein 216
UniProt accessionQ9P0N5
GeneTMEM216
OrganismHomo sapiens
Length145 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 (72)

Diseases linked to this target (Open Targets).

  • Joubert syndrome · score 0.77
  • Meckel syndrome · score 0.73
  • Joubert syndrome with oculorenal defect · score 0.62
  • genetic disorder · score 0.44
  • orofaciodigital syndrome type 6 · score 0.37
  • Abnormality of the nervous system · score 0.27
  • refractive error measurement · score 0.14
  • Microcephaly · score 0.11
  • body height · score 0.07
  • Jeune syndrome · score 0.04

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9P0N5-F1alphafoldPREDICTED89.09—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9P0N5.

Amino-acid sequence (145 residues)

MLPRGLKMAP RGKRLSSTPL EILFFLNGWY NATYFLLELF IFLYKGVLLP YPTANLVLDV VMLLLYLGIE VIRLFFGTKG NLCQRKMPLS ISVALTFPSA MMASYYLLLQ TYVLRLEAIM NGILLFFCGS ELLLEVLTLA AFSRI

Frequently asked questions

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

Which diseases are associated with TMEM216?

The strongest Open Targets associations for TMEM216 are Joubert syndrome, Meckel syndrome, Joubert syndrome with oculorenal defect, genetic disorder and orofaciodigital syndrome type 6.

How long is the TMEM216 protein?

The Homo sapiens TMEM216 protein (UniProt Q9P0N5) is 145 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

UniProtQ9P0N5
GeneTMEM216
OrganismHomo sapiens
Length145
Binders0
Diseases72
View on UniProt