Retinitis pigmentosa 9 protein (RP9)

Homo sapiens — UniProt Q8TA86

Gene: RP9Homo sapiensSwissProt reviewed

About Retinitis pigmentosa 9 protein

Retinitis pigmentosa 9 protein (RP9) is a protein from Homo sapiens identified by UniProt accession Q8TA86, 221 residues long. MolForge cross-references it against 0 known binders and 43 disease associations.

Target properties

Protein nameRetinitis pigmentosa 9 protein
UniProt accessionQ8TA86
GeneRP9
OrganismHomo sapiens
Length221 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 (43)

Diseases linked to this target (Open Targets).

  • retinitis pigmentosa · score 0.64
  • autosomal dominant retinitis pigmentosa · score 0.37
  • neurodegenerative disease · score 0.31
  • Red cell distribution width · score 0.29
  • body height · score 0.27
  • Retinal dystrophy · score 0.18
  • brain measurement · score 0.10
  • cortical surface area measurement · score 0.09
  • neuroimaging measurement · score 0.09
  • cortical thickness · score 0.09

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8TA86-F1alphafoldPREDICTED77.73—

Amino-acid sequence (221 residues)

MSSRPGREDV GAAGARRPRE PPEQELQRRR EQKRRRHDAQ QLQQLKHLES FYEKPPPGLI KEDETKPEDC IPDVPGNEHA REFLAHAPTK GLWMPLGKEV KVMQCWRCKR YGHRTGDKEC PFFIKGNQKL EQFRVAHEDP MYDIIRDNKR HEKDVRIQQL KQLLEDSTSD EDRSSSSSSE GKEKHKKKKK KEKHKKRKKE KKKKKKRKHK SSKSNEGSDS E

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Quick facts

UniProtQ8TA86
GeneRP9
OrganismHomo sapiens
Length221
Binders0
Diseases43
View on UniProt