Midnolin (MIDN)

Homo sapiens — UniProt Q504T8

Gene: MIDNHomo sapiensSwissProt reviewed

About Midnolin

Midnolin (MIDN) is a protein from Homo sapiens identified by UniProt accession Q504T8, 468 residues long. MolForge cross-references it against 0 known binders and 70 disease associations.

Target properties

Protein nameMidnolin
UniProt accessionQ504T8
GeneMIDN
OrganismHomo sapiens
Length468 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 (70)

Diseases linked to this target (Open Targets).

  • mean corpuscular volume · score 0.32
  • mean corpuscular hemoglobin concentration · score 0.30
  • mean corpuscular hemoglobin · score 0.28
  • hair color · score 0.24
  • erythrocyte count · score 0.23
  • total blood protein measurement · score 0.22
  • Varicose veins · score 0.21
  • red blood cell density measurement · score 0.09
  • hepatocellular carcinoma · score 0.07
  • cleft palate-lateral synechia syndrome · score 0.06

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q504T8-F1alphafoldPREDICTED64.95—

Amino-acid sequence (468 residues)

MEPQPGGARS CRRGAPGGAC ELGPAAEAAP MSLAIHSTTG TRYDLAVPPD ETVEGLRKRL SQRLKVPKER LALLHKDTRL SSGKLQEFGV GDGSKLTLVP TVEAGLMSQA SRPEQSVMQA LESLTETQVS DFLSGRSPLT LALRVGDHMM FVQLQLAAQH APLQHRHVLA AAAAAAAARG DPSIASPVSS PCRPVSSAAR VPPVPTSPSP ASPSPITAGS FRSHAASTTC PEQMDCSPTA SSSASPGAST TSTPGASPAP RSRKPGAVIE SFVNHAPGVF SGTFSGTLHP NCQDSSGRPR RDIGTILQIL NDLLSATRHY QGMPPSLAQL RCHAQCSPAS PAPDLAPRTT SCEKLTAAPS ASLLQGQSQI RMCKPPGDRL RQTENRATRC KVERLQLLLQ QKRLRRKARR DARGPYHWSP SRKAGRSDSS SSGGGGSPSE ASGLGLDFED SVWKPEVNPD IKSEFVVA

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Quick facts

UniProtQ504T8
GeneMIDN
OrganismHomo sapiens
Length468
Binders0
Diseases70
View on UniProt