Geminin (GMNN)

Homo sapiens — UniProt O75496

Gene: GMNNHomo sapiensSwissProt reviewed

About Geminin

Geminin (GMNN) is a protein from Homo sapiens identified by UniProt accession O75496, 209 residues long. MolForge cross-references it against 0 known binders and 207 disease associations.

Target properties

Protein nameGeminin
UniProt accessionO75496
GeneGMNN
OrganismHomo sapiens
Length209 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 (207)

Diseases linked to this target (Open Targets).

  • Ear-patella-short stature syndrome · score 0.69
  • Meier-Gorlin syndrome · score 0.45
  • neurodegenerative disease · score 0.37
  • microcephalic primordial dwarfism · score 0.37
  • lysosomal storage disease · score 0.29
  • genetic disorder · score 0.17
  • body mass index · score 0.12
  • neoplasm · score 0.11
  • early-onset non-syndromic cataract · score 0.10
  • isolated ectopia lentis · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O75496-F1alphafoldPREDICTED69.53—

Amino-acid sequence (209 residues)

MNPSMKQKQE EIKENIKNSS VPRRTLKMIQ PSASGSLVGR ENELSAGLSK RKHRNDHLTS TTSSPGVIVP ESSENKNLGG VTQESFDLMI KENPSSQYWK EVAEKRRKAL YEALKENEKL HKEIEQKDNE IARLKKENKE LAEVAEHVQY MAELIERLNG EPLDNFESLD NQEFDSEEET VEDSLVEDSE IGTCAEGTVS SSTDAKPCI

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Quick facts

UniProtO75496
GeneGMNN
OrganismHomo sapiens
Length209
Binders0
Diseases207
View on UniProt