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Sorting nexin-12 (SNX12)

Homo sapiens — UniProt Q9UMY4

Gene: SNX12Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Sorting nexin-12 (SNX12) is a protein from Homo sapiens identified by UniProt accession Q9UMY4, 162 residues long. MolForge cross-references it against 0 known binders and 49 disease associations.

  • UniProt accession: Q9UMY4; gene symbol SNX12.
  • Organism: Homo sapiens.
  • Length: 162 amino acids.
  • Top disease associations (Open Targets): Romano-Ward syndrome, familial atrial fibrillation and Brugada syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameSorting nexin-12
UniProt accessionQ9UMY4
GeneSNX12
OrganismHomo sapiens
Length162 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 (49)

Diseases linked to this target (Open Targets).

  • Romano-Ward syndrome · score 0.07
  • familial atrial fibrillation · score 0.07
  • Brugada syndrome · score 0.07
  • Familial short QT syndrome · score 0.06
  • Arrhythmogenic right ventricular dysplasia · score 0.06
  • hypertrophic cardiomyopathy · score 0.05
  • Brugada syndrome 9 · score 0.05
  • Wolff-Parkinson-White Syndrome · score 0.05
  • familial sick sinus syndrome · score 0.05
  • Brugada syndrome 3 · score 0.05

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9UMY4-F1alphafoldPREDICTED90.65—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9UMY4.

Amino-acid sequence (162 residues)

MSDTAVADTR RLNSKPQDLT DAYGPPSNFL EIDIFNPQTV GVGRARFTTY EVRMRTNLPI FKLKESCVRR RYSDFEWLKN ELERDSKIVV PPLPGKALKR QLPFRGDEGI FEESFIEERR QGLEQFINKI AGHPLAQNER CLHMFLQEEA IDRNYVPGKV RQ

Frequently asked questions

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

Which diseases are associated with SNX12?

The strongest Open Targets associations for SNX12 are Romano-Ward syndrome, familial atrial fibrillation, Brugada syndrome, Familial short QT syndrome and Arrhythmogenic right ventricular dysplasia.

How long is the SNX12 protein?

The Homo sapiens SNX12 protein (UniProt Q9UMY4) is 162 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

UniProtQ9UMY4
GeneSNX12
OrganismHomo sapiens
Length162
Binders0
Diseases49
View on UniProt