General Information of Drug Off-Target (DOT) (ID: OTCVZRG6)

DOT Name Codanin-1 (CDAN1)
Gene Name CDAN1
Related Disease
Anemia, congenital dyserythropoietic, type 1a ( )
Diabetic kidney disease ( )
Mycoses ( )
Neonatal anemia ( )
Renal fibrosis ( )
Alpha thalassemia ( )
Ankylosing spondylitis ( )
Congenital anemia ( )
Granular corneal dystrophy type II ( )
Hemoglobin H disease ( )
Hereditary haemolytic anemia ( )
Inflammatory bowel disease ( )
Irritable bowel syndrome ( )
Knee osteoarthritis ( )
Late-onset Parkinson disease ( )
Noonan syndrome ( )
Obesity ( )
Psoriatic arthritis ( )
Rheumatoid arthritis ( )
Syndactyly ( )
Thrombocytopenia ( )
Ulcerative colitis ( )
Unilateral multicystic dysplastic kidney ( )
Leukopenia ( )
Congenital dyserythropoietic anemia type 1 ( )
Arrhythmia ( )
Bipolar disorder ( )
Congenital dyserythropoietic anemia ( )
Crohn disease ( )
Oral mucositis ( )
UniProt ID
CDAN1_HUMAN
3D Structure
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2D Sequence (FASTA)
Download
3D Structure (PDB)
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Pfam ID
PF15296
Sequence
MAAVLESLLREEVSVAAVVRWIARSTQGSEDNAGEAAALSSLRALRKEFVPFLLNFLREQ
SSRVLPQGPPTPAKTPGASAALPGRPGGPPRGSRGARSQLFPPTEAQSTAAEAPLARRGG
RRRGPGPARERGGRGLEEGVSGESLPGAGGRRLRGSGSPSRPSLTLSDPPNLSNLEEFPP
VGSVPPGPTGTKPSRRINPTPVSEERSLSKPKTCFTSPPISCVPSSQPSALDTSPWGLGL
PPGCRSLQEEREMLRKERSKQLQQSPTPTCPTPELGSPLPSRTGSLTDEPADPARVSSRQ
RLELVALVYSSCIAENLVPNLFLELFFVFQLLTARRMVTAKDSDPELSPAVLDSLESPLF
QSIHDCVFFAVQVLECHFQVLSNLDKGTLKLLAENERLLCFSPALQGRLRAAYEGSVAKV
SLVMPPSTQAVSFQPETDNRANFSSDRAFHTFKKQRDVFYEVLREWEDHHEEPGWDFEKG
LGSRIRAMMGQLSAACSHSHFVRLFQKQLLQMCQSPGGAGGTVLGEAPDVLSMLGADKLG
RLWRLQERLMAPQSSGGPCPPPTFPGCQGFFRDFILSASSFQFNQHLMDSLSLKIQELNG
LALPQHEPNDEDGESDVDWQGERKQFAVVLLSLRLLAKFLGFVAFLPYRGPEPPPTGELQ
DSILALRSQVPPVLDVRTLLQRGLQARRAVLTVPWLVEFLSFADHVVPLLEYYRDIFTLL
LRLHRSLVLSQESEGKMCFLNKLLLLAVLGWLFQIPTVPEDLFFLEEGPSYAFEVDTVAP
EHGLDNAPVVDQQLLYTCCPYIGELRKLLASWVSGSSGRSGGFMRKITPTTTTSLGAQPS
QTSQGLQAQLAQAFFHNQPPSLRRTVEFVAERIGSNCVKHIKATLVADLVRQAESLLQEQ
LVTQGEEGGDPAQLLEILCSQLCPHGAQALALGREFCQRKSPGAVRALLPEETPAAVLSS
AENIAVGLATEKACAWLSANITALIRREVKAAVSRTLRAQGPEPAARGERRGCSRACEHH
APLPSHLISEIKDVLSLAVGPRDPDEGVSPEHLEQLLGQLGQTLRCRQFLCPPAEQHLAK
CSVELASLLVADQIPILGPPAQYRLERGQARRLLHMLLSLWKEDFQGPVPLQLLLSPRNV
GLLADTRPREWDLLLFLLRELVEKGLMGRMEIEACLGSLHQAQWPGDFAEELATLSNLFL
AEPHLPEPQLRACELVQPNRGTVLAQS
Function May act as a negative regulator of ASF1 in chromatin assembly.
Tissue Specificity Ubiquitously expressed. Isoform 3 is not found in erythroid cells.

Molecular Interaction Atlas (MIA) of This DOT

30 Disease(s) Related to This DOT
Disease Name Disease ID Evidence Level Mode of Inheritance REF
Anemia, congenital dyserythropoietic, type 1a DISJZNT8 Definitive Autosomal recessive [1]
Diabetic kidney disease DISJMWEY Definitive Biomarker [2]
Mycoses DIS9K7PB Definitive Biomarker [3]
Neonatal anemia DISPFC78 Definitive Biomarker [4]
Renal fibrosis DISMHI3I Definitive Biomarker [2]
Alpha thalassemia DIS5XGK0 Strong Altered Expression [5]
Ankylosing spondylitis DISRC6IR Strong Altered Expression [6]
Congenital anemia DISTW0J6 Strong Biomarker [5]
Granular corneal dystrophy type II DISAEE20 Strong Genetic Variation [7]
Hemoglobin H disease DISHFWO5 Strong Altered Expression [5]
Hereditary haemolytic anemia DIS487SI Strong Genetic Variation [8]
Inflammatory bowel disease DISGN23E Strong Biomarker [6]
Irritable bowel syndrome DIS27206 Strong Biomarker [6]
Knee osteoarthritis DISLSNBJ Strong Altered Expression [9]
Late-onset Parkinson disease DIS9IOUI Strong Biomarker [10]
Noonan syndrome DIS7Q7DN Strong Genetic Variation [11]
Obesity DIS47Y1K Strong Genetic Variation [12]
Psoriatic arthritis DISLWTG2 Strong Biomarker [13]
Rheumatoid arthritis DISTSB4J Strong Biomarker [14]
Syndactyly DISZK2BT Strong Genetic Variation [15]
Thrombocytopenia DISU61YW Strong Biomarker [16]
Ulcerative colitis DIS8K27O Strong Biomarker [17]
Unilateral multicystic dysplastic kidney DISUYQ0C Strong Genetic Variation [18]
Leukopenia DISJMBMM moderate Biomarker [19]
Congenital dyserythropoietic anemia type 1 DISCBVO6 Supportive Autosomal recessive [20]
Arrhythmia DISFF2NI Limited Biomarker [21]
Bipolar disorder DISAM7J2 Limited Genetic Variation [22]
Congenital dyserythropoietic anemia DIS6FAT6 Limited Autosomal recessive [23]
Crohn disease DIS2C5Q8 Limited Altered Expression [24]
Oral mucositis DISS93V5 Limited Biomarker [25]
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⏷ Show the Full List of 30 Disease(s)
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DOT
7 Drug(s) Affected the Gene/Protein Processing of This DOT
Drug Name Drug ID Highest Status Interaction REF
Doxorubicin DMVP5YE Approved Doxorubicin decreases the expression of Codanin-1 (CDAN1). [26]
Cisplatin DMRHGI9 Approved Cisplatin increases the expression of Codanin-1 (CDAN1). [27]
Hydrogen peroxide DM1NG5W Approved Hydrogen peroxide affects the expression of Codanin-1 (CDAN1). [28]
Leflunomide DMR8ONJ Phase 1 Trial Leflunomide decreases the expression of Codanin-1 (CDAN1). [30]
PMID28460551-Compound-2 DM4DOUB Patented PMID28460551-Compound-2 increases the expression of Codanin-1 (CDAN1). [31]
Bisphenol A DM2ZLD7 Investigative Bisphenol A decreases the expression of Codanin-1 (CDAN1). [33]
chloropicrin DMSGBQA Investigative chloropicrin increases the expression of Codanin-1 (CDAN1). [34]
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⏷ Show the Full List of 7 Drug(s)
2 Drug(s) Affected the Post-Translational Modifications of This DOT
Drug Name Drug ID Highest Status Interaction REF
Benzo(a)pyrene DMN7J43 Phase 1 Benzo(a)pyrene affects the methylation of Codanin-1 (CDAN1). [29]
PMID28870136-Compound-52 DMFDERP Patented PMID28870136-Compound-52 increases the phosphorylation of Codanin-1 (CDAN1). [32]
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References

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2 Targeting the CDA1/CDA1BP1 Axis Retards Renal Fibrosis in Experimental Diabetic Nephropathy.Diabetes. 2019 Feb;68(2):395-408. doi: 10.2337/db18-0712. Epub 2018 Nov 13.
3 Cryptococcus neoformans Cda1 and Its Chitin Deacetylase Activity Are Required for Fungal Pathogenesis.mBio. 2018 Nov 20;9(6):e02087-18. doi: 10.1128/mBio.02087-18.
4 Neonatal manifestations of congenital dyserythropoietic anemia type I.J Pediatr. 1997 Jul;131(1 Pt 1):95-7. doi: 10.1016/s0022-3476(97)70130-6.
5 A novel case of haemoglobin H disease associated with clinical and morphological characteristics of congenital dyserythropoietic anaemia type I.Eur J Haematol. 2002 Apr;68(4):247-52. doi: 10.1034/j.1600-0609.2002.01590.x.
6 The appearance of joint manifestations in the Swiss inflammatory bowel disease cohort.PLoS One. 2019 Apr 30;14(4):e0211554. doi: 10.1371/journal.pone.0211554. eCollection 2019.
7 Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1. Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14.
8 Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.Int J Hematol. 2013 May;97(5):650-3. doi: 10.1007/s12185-013-1338-4. Epub 2013 Apr 19.
9 Rheumatoid Arthritis Flares After Total Hip and Total Knee Arthroplasty: Outcomes at One Year.Arthritis Care Res (Hoboken). 2020 Jul;72(7):925-932. doi: 10.1002/acr.24091. Epub 2020 May 14.
10 Musculoskeletal ultrasound as a biomarker of remission - results from a one-year prospective study in patients with rheumatoid arthritis.Med Ultrason. 2018 Dec 8;20(4):453-460. doi: 10.11152/mu-1609.
11 Unusual dysmorphic features in five patients with Noonan's syndrome: a brief review.J Paediatr Child Health. 2002 Oct;38(5):521-5. doi: 10.1046/j.1440-1754.2002.00027.x.
12 Influence of obesity, age, and comorbidities on the multi-biomarker disease activity test in rheumatoid arthritis.Semin Arthritis Rheum. 2018 Feb;47(4):472-477. doi: 10.1016/j.semarthrit.2017.07.010. Epub 2017 Aug 2.
13 Discordance between tender and swollen joint count as well as patient's and evaluator's global assessment may reduce likelihood of remission in patients with rheumatoid arthritis and psoriatic arthritis: data from the prospective multicentre NOR-DMARD study.Ann Rheum Dis. 2017 Apr;76(4):708-711. doi: 10.1136/annrheumdis-2016-210283. Epub 2016 Oct 4.
14 Comparative effectiveness of TNF inhibitors and tocilizumab with and without conventional synthetic disease-modifying antirheumatic drugs in a pan-European observational cohort of bio-nave patients with rheumatoid arthritis.Semin Arthritis Rheum. 2020 Feb;50(1):17-24. doi: 10.1016/j.semarthrit.2019.06.020. Epub 2019 Jun 28.
15 Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.Ann Hematol. 2008 Sep;87(9):751-4. doi: 10.1007/s00277-008-0519-3. Epub 2008 Jun 25.
16 Alpha Particle Radium 223 Dichloride in High-risk Osteosarcoma: A Phase I Dose Escalation Trial.Clin Cancer Res. 2019 Jul 1;25(13):3802-3810. doi: 10.1158/1078-0432.CCR-18-3964. Epub 2019 Feb 7.
17 Efficacy of noninvasive evaluations in monitoring inflammatory bowel disease activity: A prospective study in China.World J Gastroenterol. 2017 Dec 14;23(46):8235-8247. doi: 10.3748/wjg.v23.i46.8235.
18 Dyserythropoiesis in a child with pyruvate kinase deficiency and coexistent unilateral multicystic dysplastic kidney.Pediatr Blood Cancer. 2014 Aug;61(8):1463-5. doi: 10.1002/pbc.24953. Epub 2014 Jan 30.
19 A phase I dose-escalation study of selumetinib in combination with docetaxel or dacarbazine in patients with advanced solid tumors.BMC Cancer. 2017 Mar 6;17(1):173. doi: 10.1186/s12885-017-3143-6.
20 Clinical Practice Guidelines for Rare Diseases: The Orphanet Database. PLoS One. 2017 Jan 18;12(1):e0170365. doi: 10.1371/journal.pone.0170365. eCollection 2017.
21 Protective Effects of Danlou Tablet () against Murine Myocardial Ischemia and Reperfusion Injury In Vivo.Chin J Integr Med. 2018 Aug;24(8):613-620. doi: 10.1007/s11655-016-2448-7. Epub 2016 Mar 21.
22 Genome-wide association study identifies 30 loci associated with bipolar disorder.Nat Genet. 2019 May;51(5):793-803. doi: 10.1038/s41588-019-0397-8. Epub 2019 May 1.
23 PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels. Nat Genet. 2019 Nov;51(11):1560-1565. doi: 10.1038/s41588-019-0528-2.
24 Treatment sequence network meta-analysis in Crohn's disease: a methodological case study.Curr Med Res Opin. 2019 May;35(5):733-756. doi: 10.1080/03007995.2019.1580094. Epub 2019 Mar 20.
25 Phase I study of resminostat, an HDAC inhibitor, combined with S-1 in patients with pre-treated biliary tract or pancreatic cancer.Invest New Drugs. 2019 Feb;37(1):109-117. doi: 10.1007/s10637-018-0634-5. Epub 2018 Jul 11.
26 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.
27 Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
28 Minimal peroxide exposure of neuronal cells induces multifaceted adaptive responses. PLoS One. 2010 Dec 17;5(12):e14352. doi: 10.1371/journal.pone.0014352.
29 Air pollution and DNA methylation alterations in lung cancer: A systematic and comparative study. Oncotarget. 2017 Jan 3;8(1):1369-1391. doi: 10.18632/oncotarget.13622.
30 Endoplasmic reticulum stress and MAPK signaling pathway activation underlie leflunomide-induced toxicity in HepG2 Cells. Toxicology. 2017 Dec 1;392:11-21.
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 Quantitative phosphoproteomics reveal cellular responses from caffeine, coumarin and quercetin in treated HepG2 cells. Toxicol Appl Pharmacol. 2022 Aug 15;449:116110. doi: 10.1016/j.taap.2022.116110. Epub 2022 Jun 7.
33 Bisphenol A induces DSB-ATM-p53 signaling leading to cell cycle arrest, senescence, autophagy, stress response, and estrogen release in human fetal lung fibroblasts. Arch Toxicol. 2018 Apr;92(4):1453-1469.
34 Transcriptomic analysis of human primary bronchial epithelial cells after chloropicrin treatment. Chem Res Toxicol. 2015 Oct 19;28(10):1926-35.