Clarin-1 (CLRN1)

Homo sapiens — UniProt P58418

Gene: CLRN1Homo sapiensSwissProt reviewed

About Clarin-1

Clarin-1 (CLRN1) is a protein from Homo sapiens identified by UniProt accession P58418, 232 residues long. MolForge cross-references it against 0 known binders and 90 disease associations.

Target properties

Protein nameClarin-1
UniProt accessionP58418
GeneCLRN1
OrganismHomo sapiens
Length232 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 (90)

Diseases linked to this target (Open Targets).

  • Usher syndrome type 3A · score 0.77
  • retinitis pigmentosa · score 0.75
  • Usher syndrome type 3 · score 0.70
  • Retinal dystrophy · score 0.53
  • Rare genetic deafness · score 0.53
  • Usher syndrome · score 0.52
  • hearing loss · score 0.37
  • Hearing impairment · score 0.35
  • neutrophil count · score 0.33
  • myeloid white cell count · score 0.31

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P58418-F1alphafoldPREDICTED90.75—

Amino-acid sequence (232 residues)

MPSQQKKIIF CMAGVFSFAC ALGVVTALGT PLWIKATVLC KTGALLVNAS GQELDKFMGE MQYGLFHGEG VRQCGLGARP FRFSFFPDLL KAIPVSIHVN VILFSAILIV LTMVGTAFFM YNAFGKPFET LHGPLGLYLL SFISGSCGCL VMILFASEVK IHHLSEKIAN YKEGTYVYKT QSEKYTTSFW VIFFCFFVHF LNGLLIRLAG FQFPFAKSKD AETTNVAADL MY

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Quick facts

UniProtP58418
GeneCLRN1
OrganismHomo sapiens
Length232
Binders0
Diseases90
View on UniProt