Chloride channel protein 2 (CLCN2)

Homo sapiens — UniProt P51788

Gene: CLCN2Homo sapiensSwissProt reviewed

About Chloride channel protein 2

Chloride channel protein 2 (CLCN2) is a protein from Homo sapiens identified by UniProt accession P51788, 898 residues long. MolForge cross-references it against 0 known binders and 339 disease associations.

Target properties

Protein nameChloride channel protein 2
UniProt accessionP51788
GeneCLCN2
OrganismHomo sapiens
Length898 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—

Approved drugs hitting this target (1)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (339)

Diseases linked to this target (Open Targets).

  • leukoencephalopathy with mild cerebellar ataxia and white matter edema · score 0.80
  • familial hyperaldosteronism type II · score 0.76
  • Constipation · score 0.59
  • irritable bowel syndrome · score 0.56
  • constipation disorder · score 0.50
  • juvenile myoclonic epilepsy · score 0.37
  • Parkinson disease · score 0.37
  • Chronic pain · score 0.37
  • bowel dysfunction · score 0.37
  • platelet count · score 0.31

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P51788-F1alphafoldPREDICTED72.74—

Amino-acid sequence (898 residues)

MAAAAAEEGM EPRALQYEQT LMYGRYTQDL GAFAKEEAAR IRLGGPEPWK GPPSSRAAPE LLEYGRSRCA RCRVCSVRCH KFLVSRVGED WIFLVLLGLL MALVSWVMDY AIAACLQAQQ WMSRGLNTSI LLQYLAWVTY PVVLITFSAG FTQILAPQAV GSGIPEMKTI LRGVVLKEYL TLKTFIAKVI GLTCALGSGM PLGKEGPFVH IASMCAALLS KFLSLFGGIY ENESRNTEML AAACAVGVGC CFAAPIGGVL FSIEVTSTFF AVRNYWRGFF AATFSAFIFR VLAVWNRDEE TITALFKTRF RLDFPFDLQE LPAFAVIGIA SGFGGALFVY LNRKIVQVMR KQKTINRFLM RKRLLFPALV TLLISTLTFP PGFGQFMAGQ LSQKETLVTL FDNRTWVRQG LVEELEPPST SQAWNPPRAN VFLTLVIFIL MKFWMSALAT TIPVPCGAFM PVFVIGAAFG RLVGESMAAW FPDGIHTDSS TYRIVPGGYA VVGAAALAGA VTHTVSTAVI VFELTGQIAH ILPVMIAVIL ANAVAQSLQP SLYDSIIRIK KLPYLPELGW GRHQQYRVRV EDIMVRDVPH VALSCTFRDL RLALHRTKGR MLALVESPES MILLGSIERS QVVALLGAQL SPARRRQHMQ ERRATQTSPL SDQEGPPTPE ASVCFQVNTE DSAFPAARGE THKPLKPALK RGPSVTRNLG ESPTGSAESA GIALRSLFCG SPPPEAASEK LESCEKRKLK RVRISLASDA DLEGEMSPEE ILEWEEQQLD EPVNFSDCKI DPAPFQLVER TSLHKTHTIF SLLGVDHAYV TSIGRLIGIV TLKELRKAIE GSVTAQGVKV RPPLASFRDS ATSSSDTETT EVHALWGPHS RHGLPREGSP SDSDDKCQ

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Quick facts

UniProtP51788
GeneCLCN2
OrganismHomo sapiens
Length898
Binders0
Diseases339
View on UniProt