General Information of Drug Off-Target (DOT) (ID: OTC7R3YL)

DOT Name MORN repeat-containing protein 5 (MORN5)
Gene Name MORN5
Related Disease
Lung squamous cell carcinoma ( )
Isolated cleft palate ( )
UniProt ID
MORN5_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Pfam ID
PF02493
Sequence
MEYTGSKYIGEYVDGRMEGKAKYILPTETIYVGEMKDGMFHGEGTLYFPSGSQYDAIWEN
GLAIKGTYTFSDGLHYDEKNWHYCDGYDRRFYTEILNGLKPAGMAQLTNMDPPRKIPKGY
YDCGDGFYNPVTRVVKDYRNRFLRNADDDEHEWITRTCRKG
Tissue Specificity Expressed in sperm (at protein level).

Molecular Interaction Atlas (MIA) of This DOT

2 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Lung squamous cell carcinoma DISXPIBD Strong Genetic Variation [1]
Isolated cleft palate DISV80CD No Known Unknown [2]
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Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
1 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the methylation of MORN repeat-containing protein 5 (MORN5). [3]
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5 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Vorinostat DMWMPD4 Approved Vorinostat increases the expression of MORN repeat-containing protein 5 (MORN5). [4]
SNDX-275 DMH7W9X Phase 3 SNDX-275 increases the expression of MORN repeat-containing protein 5 (MORN5). [4]
Fenfluramine DM0762O Phase 3 Fenfluramine increases the expression of MORN repeat-containing protein 5 (MORN5). [5]
Amiodarone DMUTEX3 Phase 2/3 Trial Amiodarone increases the expression of MORN repeat-containing protein 5 (MORN5). [6]
Acetaldehyde DMJFKG4 Investigative Acetaldehyde increases the expression of MORN repeat-containing protein 5 (MORN5). [7]
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References

1 Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.Lancet Respir Med. 2019 Oct;7(10):881-891. doi: 10.1016/S2213-2600(19)30144-4. Epub 2019 Jul 17.
2 MORN5 Expression during Craniofacial Development and Its Interaction with the BMP and TGF Pathways. Front Physiol. 2016 Aug 31;7:378. doi: 10.3389/fphys.2016.00378. eCollection 2016.
3 Integrative omics data analyses of repeated dose toxicity of valproic acid in vitro reveal new mechanisms of steatosis induction. Toxicology. 2018 Jan 15;393:160-170.
4 Definition of transcriptome-based indices for quantitative characterization of chemically disturbed stem cell development: introduction of the STOP-Toxukn and STOP-Toxukk tests. Arch Toxicol. 2017 Feb;91(2):839-864.
5 Fenfluramine-induced gene dysregulation in human pulmonary artery smooth muscle and endothelial cells. Pulm Circ. 2011 Jul-Sep;1(3):405-18. doi: 10.4103/2045-8932.87310.
6 Identification by automated screening of a small molecule that selectively eliminates neural stem cells derived from hESCs but not dopamine neurons. PLoS One. 2009 Sep 23;4(9):e7155.
7 Transcriptome profile analysis of saturated aliphatic aldehydes reveals carbon number-specific molecules involved in pulmonary toxicity. Chem Res Toxicol. 2014 Aug 18;27(8):1362-70.