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TBC1 domain family member 23 (TBC1D23)

Homo sapiens — UniProt Q9NUY8

Gene: TBC1D23Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

TBC1 domain family member 23 (TBC1D23) is a protein from Homo sapiens identified by UniProt accession Q9NUY8, 699 residues long. MolForge cross-references it against 0 known binders and 23 disease associations.

  • UniProt accession: Q9NUY8; gene symbol TBC1D23.
  • Organism: Homo sapiens.
  • Length: 699 amino acids.
  • Top disease associations (Open Targets): Non-syndromic pontocerebellar hypoplasia, pontocerebellar hypoplasia and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameTBC1 domain family member 23
UniProt accessionQ9NUY8
GeneTBC1D23
OrganismHomo sapiens
Length699 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 (23)

Diseases linked to this target (Open Targets).

  • Non-syndromic pontocerebellar hypoplasia · score 0.71
  • pontocerebellar hypoplasia · score 0.46
  • genetic disorder · score 0.41
  • Intellectual disability · score 0.37
  • neurodegenerative disease · score 0.34
  • BMI-adjusted waist circumference · score 0.14
  • refractive error · score 0.08
  • non-small cell lung carcinoma · score 0.07
  • drug use measurement · score 0.06
  • facial morphology measurement · score 0.04

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NUY8-F1alphafoldPREDICTED80.07—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NUY8.

Amino-acid sequence (699 residues)

MAEGEDVPPL PTSSGDGWEK DLEEALEAGG CDLETLRNII QGRPLPADLR AKVWKIALNV AGKGDSLASW DGILDLPEQN TIHKDCLQFI DQLSVPEEKA AELLLDIESV ITFYCKSRNI KYSTSLSWIH LLKPLVHLQL PRSDLYNCFY AIMNKYIPRD CSQKGRPFHL FRLLIQYHEP ELCSYLDTKK ITPDSYALNW LGSLFACYCS TEVTQAIWDG YLQQADPFFI YFLMLIILVN AKEVILTQES DSKEEVIKFL ENTPSSLNIE DIEDLFSLAQ YYCSKTPASF RKDNHHLFGS TLLGIKDDDA DLSQALCLAI SVSEILQANQ LQGEGVRFFV VDCRPAEQYN AGHLSTAFHL DSDLMLQNPS EFAQSVKSLL EAQKQSIESG SIAGGEHLCF MGSGREEEDM YMNMVLAHFL QKNKEYVSIA SGGFMALQQH LADINVDGPE NGYGHWIAST SGSRSSINSV DGESPNGSSD RGMKSLVNKM TVALKTKSVN VREKVISFIE NTSTPVDRMS FNLPWPDRSC TERHVSSSDR VGKPYRGVKP VFSIGDEEEY DTDEIDSSSM SDDDRKEVVN IQTWINKPDV KHHFPCKEVK ESGHMFPSHL LVTATHMYCL REIVSRKGLA YIQSRQALNS VVKITSKKKH PELITFKYGN SSASGIEILA IERYLIPNAG DATKAIKQQI MKVLDALES

Frequently asked questions

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

Which diseases are associated with TBC1D23?

The strongest Open Targets associations for TBC1D23 are Non-syndromic pontocerebellar hypoplasia, pontocerebellar hypoplasia, genetic disorder, Intellectual disability and neurodegenerative disease.

How long is the TBC1D23 protein?

The Homo sapiens TBC1D23 protein (UniProt Q9NUY8) is 699 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

UniProtQ9NUY8
GeneTBC1D23
OrganismHomo sapiens
Length699
Binders0
Diseases23
View on UniProt