General Information of Drug Off-Target (DOT) (ID: OT7QO47I)

DOT Name Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L)
Gene Name RABGAP1L
Related Disease
Benign prostatic hyperplasia ( )
Esophageal squamous cell carcinoma ( )
High blood pressure ( )
Klinefelter syndrome ( )
Major depressive disorder ( )
Melanoma ( )
Migraine disorder ( )
Mood disorder ( )
Prostate cancer ( )
Prostate carcinoma ( )
Systemic lupus erythematosus ( )
UniProt ID
RBG10_HUMAN
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MIENSSWSMTFEERENRRLQEASMRLEQENDDLAHELVTSKIALRNDLDQAEDKADVLNK
ELLLTKQRLVETEEEKRKQEEETAQLKEVFRKQLEKAEYEIKKTTAIIAEYKQICSQLST
RLEKQQAASKEELEVVKGKMMACKHCSDIFSKEGALKLAATGREDQGIETDDEKDSLKKQ
LREMELELAQTKLQLVEAKCKIQELEHQRGALMNEIQAAKNSWFSKTLNSIKTATGTQPL
QPAPVTQPPKEST

Molecular Interaction Atlas (MIA) of This DOT

11 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Benign prostatic hyperplasia DISI3CW2 Strong Altered Expression [1]
Esophageal squamous cell carcinoma DIS5N2GV Strong Altered Expression [2]
High blood pressure DISY2OHH Strong Genetic Variation [3]
Klinefelter syndrome DISOUI7W Strong Genetic Variation [4]
Major depressive disorder DIS4CL3X Strong Genetic Variation [5]
Melanoma DIS1RRCY Strong Biomarker [2]
Migraine disorder DISFCQTG Strong Genetic Variation [6]
Mood disorder DISLVMWO Strong Genetic Variation [5]
Prostate cancer DISF190Y Strong Altered Expression [1]
Prostate carcinoma DISMJPLE Strong Altered Expression [1]
Systemic lupus erythematosus DISI1SZ7 Strong Genetic Variation [7]
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⏷ Show the Full List of 11 Disease(s)
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
27 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Valproate DMCFE9I Approved Valproate decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [8]
Ciclosporin DMAZJFX Approved Ciclosporin increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [9]
Tretinoin DM49DUI Approved Tretinoin decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [10]
Acetaminophen DMUIE76 Approved Acetaminophen decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [11]
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [12]
Cupric Sulfate DMP0NFQ Approved Cupric Sulfate decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [13]
Cisplatin DMRHGI9 Approved Cisplatin decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [14]
Estradiol DMUNTE3 Approved Estradiol decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [15]
Quercetin DM3NC4M Approved Quercetin affects the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [17]
Temozolomide DMKECZD Approved Temozolomide decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [18]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [19]
Calcitriol DM8ZVJ7 Approved Calcitriol increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [20]
Vorinostat DMWMPD4 Approved Vorinostat decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [21]
Carbamazepine DMZOLBI Approved Carbamazepine affects the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [22]
Marinol DM70IK5 Approved Marinol increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [23]
Zoledronate DMIXC7G Approved Zoledronate decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [24]
Panobinostat DM58WKG Approved Panobinostat increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [25]
Hydroquinone DM6AVR4 Approved Hydroquinone decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [27]
SNDX-275 DMH7W9X Phase 3 SNDX-275 increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [25]
Resveratrol DM3RWXL Phase 3 Resveratrol decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [28]
Belinostat DM6OC53 Phase 2 Belinostat increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [25]
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [29]
(+)-JQ1 DM1CZSJ Phase 1 (+)-JQ1 decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [30]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [31]
Trichostatin A DM9C8NX Investigative Trichostatin A increases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [8]
Formaldehyde DM7Q6M0 Investigative Formaldehyde decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [32]
OXYQUINOLINE DMZVS9Y Investigative OXYQUINOLINE decreases the expression of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [17]
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⏷ Show the Full List of 27 Drug(s)
3 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Arsenic DMTL2Y1 Approved Arsenic affects the methylation of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [16]
Fulvestrant DM0YZC6 Approved Fulvestrant increases the methylation of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [26]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the methylation of Rab GTPase-activating protein 1-like, isoform 10 (RABGAP1L). [26]
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References

1 Tissue ACE phenotyping in prostate cancer.Oncotarget. 2019 Oct 29;10(59):6349-6361. doi: 10.18632/oncotarget.27276. eCollection 2019 Oct 29.
2 Transcriptional gene expression profile of human esophageal squamous cell carcinoma.Genomics. 2003 May;81(5):481-8. doi: 10.1016/s0888-7543(03)00023-5.
3 Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.Am J Hypertens. 2010 Jan;23(1):70-7. doi: 10.1038/ajh.2009.190. Epub 2009 Oct 22.
4 RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome.Virchows Arch. 2009 Mar;454(3):311-6. doi: 10.1007/s00428-009-0732-z. Epub 2009 Jan 28.
5 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.Nat Genet. 2018 Jul;50(7):920-927. doi: 10.1038/s41588-018-0151-7. Epub 2018 Jun 25.
6 Genome-wide meta-analysis identifies new susceptibility loci for migraine.Nat Genet. 2013 Aug;45(8):912-917. doi: 10.1038/ng.2676. Epub 2013 Jun 23.
7 Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.Arthritis Rheum. 2013 Apr;65(4):1055-63. doi: 10.1002/art.37854.
8 From transient transcriptome responses to disturbed neurodevelopment: role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects. Arch Toxicol. 2014 Jul;88(7):1451-68.
9 Integrating multiple omics to unravel mechanisms of Cyclosporin A induced hepatotoxicity in vitro. Toxicol In Vitro. 2015 Apr;29(3):489-501.
10 Phenotypic characterization of retinoic acid differentiated SH-SY5Y cells by transcriptional profiling. PLoS One. 2013 May 28;8(5):e63862.
11 Gene expression analysis of precision-cut human liver slices indicates stable expression of ADME-Tox related genes. Toxicol Appl Pharmacol. 2011 May 15;253(1):57-69.
12 Bringing in vitro analysis closer to in vivo: studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
13 Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
14 Low doses of cisplatin induce gene alterations, cell cycle arrest, and apoptosis in human promyelocytic leukemia cells. Biomark Insights. 2016 Aug 24;11:113-21.
15 Genistein and bisphenol A exposure cause estrogen receptor 1 to bind thousands of sites in a cell type-specific manner. Genome Res. 2012 Nov;22(11):2153-62.
16 Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015 Jan;143(1):97-106. doi: 10.1093/toxsci/kfu210. Epub 2014 Oct 10.
17 Comparison of phenotypic and transcriptomic effects of false-positive genotoxins, true genotoxins and non-genotoxins using HepG2 cells. Mutagenesis. 2011 Sep;26(5):593-604.
18 Temozolomide induces activation of Wnt/-catenin signaling in glioma cells via PI3K/Akt pathway: implications in glioma therapy. Cell Biol Toxicol. 2020 Jun;36(3):273-278. doi: 10.1007/s10565-019-09502-7. Epub 2019 Nov 22.
19 Oxidative stress modulates theophylline effects on steroid responsiveness. Biochem Biophys Res Commun. 2008 Dec 19;377(3):797-802.
20 Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes. Mol Endocrinol. 2005 Nov;19(11):2685-95.
21 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.
22 Gene Expression Regulation and Pathway Analysis After Valproic Acid and Carbamazepine Exposure in a Human Embryonic Stem Cell-Based Neurodevelopmental Toxicity Assay. Toxicol Sci. 2015 Aug;146(2):311-20. doi: 10.1093/toxsci/kfv094. Epub 2015 May 15.
23 Delta9-tetrahydrocannabinol inhibits cytotrophoblast cell proliferation and modulates gene transcription. Mol Hum Reprod. 2006 May;12(5):321-33. doi: 10.1093/molehr/gal036. Epub 2006 Apr 5.
24 Zoledronate dysregulates fatty acid metabolism in renal tubular epithelial cells to induce nephrotoxicity. Arch Toxicol. 2018 Jan;92(1):469-485.
25 A transcriptome-based classifier to identify developmental toxicants by stem cell testing: design, validation and optimization for histone deacetylase inhibitors. Arch Toxicol. 2015 Sep;89(9):1599-618.
26 DNA methylome-wide alterations associated with estrogen receptor-dependent effects of bisphenols in breast cancer. Clin Epigenetics. 2019 Oct 10;11(1):138. doi: 10.1186/s13148-019-0725-y.
27 Keratinocyte-derived IL-36gama plays a role in hydroquinone-induced chemical leukoderma through inhibition of melanogenesis in human epidermal melanocytes. Arch Toxicol. 2019 Aug;93(8):2307-2320.
28 A novel long noncoding RNA AK001796 acts as an oncogene and is involved in cell growth inhibition by resveratrol in lung cancer. Toxicol Appl Pharmacol. 2015 Jun 1;285(2):79-88.
29 Transcriptional signature of human macrophages exposed to the environmental contaminant benzo(a)pyrene. Toxicol Sci. 2010 Apr;114(2):247-59.
30 Bromodomain-containing protein 4 (BRD4) regulates RNA polymerase II serine 2 phosphorylation in human CD4+ T cells. J Biol Chem. 2012 Dec 14;287(51):43137-55.
31 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.
32 Characterization of formaldehyde's genotoxic mode of action by gene expression analysis in TK6 cells. Arch Toxicol. 2013 Nov;87(11):1999-2012.