Cone-rod homeobox protein (CRX)

Homo sapiens — UniProt O43186

Gene: CRXHomo sapiensSwissProt reviewed

About Cone-rod homeobox protein

Cone-rod homeobox protein (CRX) is a protein from Homo sapiens identified by UniProt accession O43186, 299 residues long. MolForge cross-references it against 0 known binders and 268 disease associations.

Target properties

Protein nameCone-rod homeobox protein
UniProt accessionO43186
GeneCRX
OrganismHomo sapiens
Length299 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 (268)

Diseases linked to this target (Open Targets).

  • Cone rod dystrophy · score 0.78
  • Leber congenital amaurosis · score 0.73
  • retinitis pigmentosa · score 0.71
  • autosomal dominant retinitis pigmentosa · score 0.56
  • Retinal dystrophy · score 0.56
  • neurodegenerative disease · score 0.53
  • benign concentric annular macular dystrophy · score 0.46
  • Stargardt disease · score 0.45
  • Macular dystrophy · score 0.44
  • Leber congenital amaurosis 1 · score 0.43

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O43186-F1alphafoldPREDICTED60.52—

Amino-acid sequence (299 residues)

MMAYMNPGPH YSVNALALSG PSVDLMHQAV PYPSAPRKQR RERTTFTRSQ LEELEALFAK TQYPDVYARE EVALKINLPE SRVQVWFKNR RAKCRQQRQQ QKQQQQPPGG QAKARPAKRK AGTSPRPSTD VCPDPLGISD SYSPPLPGPS GSPTTAVATV SIWSPASESP LPEAQRAGLV ASGPSLTSAP YAMTYAPASA FCSSPSAYGS PSSYFSGLDP YLSPMVPQLG GPALSPLSGP SVGPSLAQSP TSLSGQSYGA YSPVDSLEFK DPTGTWKFTY NPMDPLDYKD QSAWKFQIL

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Quick facts

UniProtO43186
GeneCRX
OrganismHomo sapiens
Length299
Binders0
Diseases268
View on UniProt