General Information of Drug Off-Target (DOT) (ID: OT2FLMUL)

DOT Name Putative claudin-24 (CLDN24)
Synonyms Claudin-21
Gene Name CLDN24
UniProt ID
CLD24_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF00822
Sequence
MALIFRTAMQSVGLLLSLLGWILSIITTYLPHWKNLNLDLNEMENWTMGLWQTCVIQEEV
GMQCKDFDSFLALPAELRVSRILMFLSNGLGFLGLLVSGFGLDCLRIGESQRDLKRRLLI
LGGILSWASGITALVPVSWVAHKTVQEFWDENVPDFVPRWEFGEALFLGWFAGLSLLLGG
CLLNCAACSSHAPLALGHYAVAQMQTQCPYLEDGTADPQV
Function Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.
KEGG Pathway
Cell adhesion molecules (hsa04514 )
Tight junction (hsa04530 )
Leukocyte transendothelial migration (hsa04670 )
Pathogenic Escherichia coli infection (hsa05130 )
Hepatitis C (hsa05160 )

Molecular Interaction Atlas (MIA) of This DOT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
2 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 increases the expression of Putative claudin-24 (CLDN24). [1]
Milchsaure DM462BT Investigative Milchsaure increases the expression of Putative claudin-24 (CLDN24). [2]
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References

1 Cell-based two-dimensional morphological assessment system to predict cancer drug-induced cardiotoxicity using human induced pluripotent stem cell-derived cardiomyocytes. Toxicol Appl Pharmacol. 2019 Nov 15;383:114761. doi: 10.1016/j.taap.2019.114761. Epub 2019 Sep 15.
2 Transcriptional profiling of lactic acid treated reconstructed human epidermis reveals pathways underlying stinging and itch. Toxicol In Vitro. 2019 Jun;57:164-173.