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Sorbitol dehydrogenase (SORD)

Homo sapiens — UniProt Q00796

Gene: SORDHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Sorbitol dehydrogenase (SORD) is a protein from Homo sapiens identified by UniProt accession Q00796, 357 residues long. MolForge cross-references it against 2 known binders and 212 disease associations.

  • UniProt accession: Q00796; gene symbol SORD.
  • Organism: Homo sapiens.
  • Length: 357 amino acids.
  • Top disease associations (Open Targets): neuronopathy, distal hereditary motor, autosomal recessive 8, genetic disorder and Charcot-Marie-Tooth disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSorbitol dehydrogenase
UniProt accessionQ00796
GeneSORD
OrganismHomo sapiens
Length357 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 (212)

Diseases linked to this target (Open Targets).

  • neuronopathy, distal hereditary motor, autosomal recessive 8 · score 0.74
  • genetic disorder · score 0.41
  • Charcot-Marie-Tooth disease · score 0.38
  • neuromuscular disease · score 0.34
  • peripheral neuropathy · score 0.27
  • Red cell distribution width · score 0.23
  • mean corpuscular hemoglobin concentration · score 0.18
  • hemoglobin measurement · score 0.16
  • MODY · score 0.10
  • early-onset non-syndromic cataract · score 0.10

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q00796-F1alphafoldPREDICTED97.98—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q00796.

Amino-acid sequence (357 residues)

MAAAAKPNNL SLVVHGPGDL RLENYPIPEP GPNEVLLRMH SVGICGSDVH YWEYGRIGNF IVKKPMVLGH EASGTVEKVG SSVKHLKPGD RVAIEPGAPR ENDEFCKMGR YNLSPSIFFC ATPPDDGNLC RFYKHNAAFC YKLPDNVTFE EGALIEPLSV GIHACRRGGV TLGHKVLVCG AGPIGMVTLL VAKAMGAAQV VVTDLSATRL SKAKEIGADL VLQISKESPQ EIARKVEGQL GCKPEVTIEC TGAEASIQAG IYATRSGGNL VLVGLGSEMT TVPLLHAAIR EVDIKGVFRY CNTWPVAISM LASKSVNVKP LVTHRFPLEK ALEAFETFKK GLGLKIMLKC DPSDQNP

Frequently asked questions

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

Which diseases are associated with SORD?

The strongest Open Targets associations for SORD are neuronopathy, distal hereditary motor, autosomal recessive 8, genetic disorder, Charcot-Marie-Tooth disease, neuromuscular disease and peripheral neuropathy.

How long is the SORD protein?

The Homo sapiens SORD protein (UniProt Q00796) is 357 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

UniProtQ00796
GeneSORD
OrganismHomo sapiens
Length357
Binders2
Diseases212
View on UniProt