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Spartin (SPART)

Homo sapiens — UniProt Q8N0X7

Gene: SPARTHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Spartin (SPART) is a protein from Homo sapiens identified by UniProt accession Q8N0X7, 666 residues long. MolForge cross-references it against 0 known binders and 78 disease associations.

  • UniProt accession: Q8N0X7; gene symbol SPART.
  • Organism: Homo sapiens.
  • Length: 666 amino acids.
  • Top disease associations (Open Targets): Troyer syndrome, Neurodevelopmental delay and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSpartin
UniProt accessionQ8N0X7
GeneSPART
OrganismHomo sapiens
Length666 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 (78)

Diseases linked to this target (Open Targets).

  • Troyer syndrome · score 0.78
  • Neurodevelopmental delay · score 0.45
  • genetic disorder · score 0.41
  • body height · score 0.31
  • Global developmental delay · score 0.26
  • Failure to thrive · score 0.26
  • cerebellar ataxia · score 0.26
  • Microcephaly · score 0.26
  • Dysarthria · score 0.26
  • Strabismus · score 0.26

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8N0X7-F1alphafoldPREDICTED62.66—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8N0X7.

Amino-acid sequence (666 residues)

MEQEPQNGEP AEIKIIREAY KKAFLFVNKG LNTDELGQKE EAKNYYKQGI GHLLRGISIS SKESEHTGPG WESARQMQQK MKETLQNVRT RLEILEKGLA TSLQNDLQEV PKLYPEFPPK DMCEKLPEPQ SFSSAPQHAE VNGNTSTPSA GAVAAPASLS LPSQSCPAEA PPAYTPQAAE GHYTVSYGTD SGEFSSVGEE FYRNHSQPPP LETLGLDADE LILIPNGVQI FFVNPAGEVS APSYPGYLRI VRFLDNSLDT VLNRPPGFLQ VCDWLYPLVP DRSPVLKCTA GAYMFPDTML QAAGCFVGVV LSSELPEDDR ELFEDLLRQM SDLRLQANWN RAEEENEFQI PGRTRPSSDQ LKEASGTDVK QLDQGNKDVR HKGKRGKRAK DTSSEEVNLS HIVPCEPVPE EKPKELPEWS EKVAHNILSG ASWVSWGLVK GAEITGKAIQ KGASKLRERI QPEEKPVEVS PAVTKGLYIA KQATGGAAKV SQFLVDGVCT VANCVGKELA PHVKKHGSKL VPESLKKDKD GKSPLDGAMV VAASSVQGFS TVWQGLECAA KCIVNNVSAE TVQTVRYKYG YNAGEATHHA VDSAVNVGVT AYNINNIGIK AMVKKTATQT GHTLLEDYQI VDNSQRENQE GAANVNVRGE KDEQTKEVKE AKKKDK

Frequently asked questions

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

Which diseases are associated with SPART?

The strongest Open Targets associations for SPART are Troyer syndrome, Neurodevelopmental delay, genetic disorder, body height and Global developmental delay.

How long is the SPART protein?

The Homo sapiens SPART protein (UniProt Q8N0X7) is 666 amino acids long.

Browse: Targets: S · 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

UniProtQ8N0X7
GeneSPART
OrganismHomo sapiens
Length666
Binders0
Diseases78
View on UniProt