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Maspardin (SPG21)

Homo sapiens — UniProt Q9NZD8

Gene: SPG21Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Maspardin (SPG21) is a protein from Homo sapiens identified by UniProt accession Q9NZD8, 308 residues long. MolForge cross-references it against 0 known binders and 20 disease associations.

  • UniProt accession: Q9NZD8; gene symbol SPG21.
  • Organism: Homo sapiens.
  • Length: 308 amino acids.
  • Top disease associations (Open Targets): mast syndrome, hereditary sensory and autonomic neuropathy with spastic paraplegia and hereditary spastic paraplegia.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameMaspardin
UniProt accessionQ9NZD8
GeneSPG21
OrganismHomo sapiens
Length308 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 (20)

Diseases linked to this target (Open Targets).

  • mast syndrome · score 0.74
  • hereditary sensory and autonomic neuropathy with spastic paraplegia · score 0.50
  • hereditary spastic paraplegia · score 0.47
  • body height · score 0.13
  • hepatocellular carcinoma · score 0.03
  • hypertrophic cardiomyopathy · score 0.02
  • tarsal-carpal coalition syndrome · score 0.01
  • neoplasm · score 0.00
  • multiple myeloma · score 0.00
  • Paraplegia · score 0.00

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NZD8-F1alphafoldPREDICTED92.83—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NZD8.

Amino-acid sequence (308 residues)

MGEIKVSPDY NWFRGTVPLK KIIVDDDDSK IWSLYDAGPR SIRCPLIFLP PVSGTADVFF RQILALTGWG YRVIALQYPV YWDHLEFCDG FRKLLDHLQL DKVHLFGASL GGFLAQKFAE YTHKSPRVHS LILCNSFSDT SIFNQTWTAN SFWLMPAFML KKIVLGNFSS GPVDPMMADA IDFMVDRLES LGQSELASRL TLNCQNSYVE PHKIRDIPVT IMDVFDQSAL STEAKEEMYK LYPNARRAHL KTGGNFPYLC RSAEVNLYVQ IHLLQFHGTK YAAIDPSMVS AEELEVQKGS LGISQEEQ

Frequently asked questions

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

Which diseases are associated with SPG21?

The strongest Open Targets associations for SPG21 are mast syndrome, hereditary sensory and autonomic neuropathy with spastic paraplegia, hereditary spastic paraplegia, body height and hepatocellular carcinoma.

How long is the SPG21 protein?

The Homo sapiens SPG21 protein (UniProt Q9NZD8) is 308 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

UniProtQ9NZD8
GeneSPG21
OrganismHomo sapiens
Length308
Binders0
Diseases20
View on UniProt