Retinoschisin (RS1)

Homo sapiens — UniProt O15537

Gene: RS1Homo sapiensSwissProt reviewed

About Retinoschisin

Retinoschisin (RS1) is a protein from Homo sapiens identified by UniProt accession O15537, 224 residues long. MolForge cross-references it against 0 known binders and 174 disease associations.

Target properties

Protein nameRetinoschisin
UniProt accessionO15537
GeneRS1
OrganismHomo sapiens
Length224 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 (174)

Diseases linked to this target (Open Targets).

  • X-linked retinoschisis · score 0.82
  • retinoschisis · score 0.63
  • Retinal dystrophy · score 0.55
  • developmental and epileptic encephalopathy, 2 · score 0.45
  • developmental and epileptic encephalopathy · score 0.45
  • genetic disorder · score 0.40
  • intellectual disability - sparse hair - brachydactyly · score 0.27
  • Angelman syndrome · score 0.19
  • atypical Rett syndrome · score 0.14
  • Epileptic encephalopathy · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O15537-F1alphafoldPREDICTED72.68—

Amino-acid sequence (224 residues)

MSRKIEGFLL LLLFGYEATL GLSSTEDEGE DPWYQKACKC DCQGGPNALW SAGATSLDCI PECPYHKPLG FESGEVTPDQ ITCSNPEQYV GWYSSWTANK ARLNSQGFGC AWLSKFQDSS QWLQIDLKEI KVISGILTQG RCDIDEWMTK YSVQYRTDER LNWIYYKDQT GNNRVFYGNS DRTSTVQNLL RPPIISRFIR LIPLGWHVRI AIRMELLECV SKCA

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Quick facts

UniProtO15537
GeneRS1
OrganismHomo sapiens
Length224
Binders0
Diseases174
View on UniProt