Dymeclin (DYM)

Homo sapiens — UniProt Q7RTS9

Gene: DYMHomo sapiensSwissProt reviewed

About Dymeclin

Dymeclin (DYM) is a protein from Homo sapiens identified by UniProt accession Q7RTS9, 669 residues long. MolForge cross-references it against 0 known binders and 268 disease associations.

Target properties

Protein nameDymeclin
UniProt accessionQ7RTS9
GeneDYM
OrganismHomo sapiens
Length669 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).

  • Dyggve-Melchior-Clausen disease · score 0.81
  • Smith-McCort dysplasia · score 0.68
  • Smith-McCort dysplasia 1 · score 0.62
  • genetic disorder · score 0.41
  • Lethal encephalopathy due to mitochondrial and peroxisomal fission defect · score 0.37
  • encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1 · score 0.37
  • lean body mass · score 0.34
  • waist-hip ratio · score 0.34
  • BMI-adjusted waist-hip ratio · score 0.33
  • body height · score 0.32

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q7RTS9-F1alphafoldPREDICTED87.06—

Amino-acid sequence (669 residues)

MGSNSSRIGD LPKNEYLKKL SGTESISEND PFWNQLLSFS FPAPTSSSEL KLLEEATISV CRSLVENNPR TGNLGALIKV FLSRTKELKL SAECQNHIFI WQTHNALFII CCLLKVFICQ MSEEELQLHF TYEEKSPGNY SSDSEDLLEE LLCCLMQLIT DIPLLDITYE ISVEAISTMV VFLSCQLFHK EVLRQSISHK YLMRGPCLPY TSKLVKTLLY NFIRQEKPPP PGAHVFPQQS DGGGLLYGLA SGVATGLWTV FTLGGVGSKA AASPELSSPL ANQSLLLLLV LANLTDASDA PNPYRQAIMS FKNTQDSSPF PSSIPHAFQI NFNSLYTALC EQQTSDQATL LLYTLLHQNS NIRTYMLART DMENLVLPIL EILYHVEERN SHHVYMALII LLILTEDDGF NRSIHEVILK NITWYSERVL TEISLGSLLI LVVIRTIQYN MTRTRDKYLH TNCLAALANM SAQFRSLHQY AAQRIISLFS LLSKKHNKVL EQATQSLRGS LSSNDVPLPD YAQDLNVIEE VIRMMLEIIN SCLTNSLHHN PNLVYALLYK RDLFEQFRTH PSFQDIMQNI DLVISFFSSR LLQAGAELSV ERVLEIIKQG VVALPKDRLK KFPELKFKYV EEEQPEEFFI PYVWSLVYNS AVGLYWNPQD IQLFTMDSD

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Quick facts

UniProtQ7RTS9
GeneDYM
OrganismHomo sapiens
Length669
Binders0
Diseases268
View on UniProt