Sorting nexin-22 (SNX22)

Homo sapiens — UniProt Q96L94

Gene: SNX22Homo sapiensSwissProt reviewed

About Sorting nexin-22

Sorting nexin-22 (SNX22) is a protein from Homo sapiens identified by UniProt accession Q96L94, 193 residues long. MolForge cross-references it against 0 known binders and 42 disease associations.

Target properties

Protein nameSorting nexin-22
UniProt accessionQ96L94
GeneSNX22
OrganismHomo sapiens
Length193 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (42)

Diseases linked to this target (Open Targets).

  • osteogenesis imperfecta · score 0.52
  • mean corpuscular volume · score 0.19
  • erythrocyte count · score 0.19
  • genetic disorder · score 0.16
  • coronary artery disease · score 0.15
  • apolipoprotein B measurement · score 0.14
  • hemoglobin measurement · score 0.14
  • mean platelet volume · score 0.14
  • monocyte percentage of leukocytes · score 0.13
  • low density lipoprotein cholesterol measurement · score 0.10

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96L94-F1alphafoldPREDICTED71.89—

Amino-acid sequence (193 residues)

MLEVHIPSVG PEAEGPRQSP EKSHMVFRVE VLCSGRRHTV PRRYSEFHAL HKRIKKLYKV PDFPSKRLPN WRTRGLEQRR QGLEAYIQGI LYLNQEVPKE LLEFLRLRHF PTDPKASNWG TLREFLPGDS SSQQHQRPVL SFHVDPYVCN PSPESLPNVV VNGVLQGLYS FSISPDKAQP KAACHPAPLP PMP

Explore Sorting nexin-22 with MolForge

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Quick facts

UniProtQ96L94
GeneSNX22
OrganismHomo sapiens
Length193
Binders0
Diseases42
View on UniProt