• rhythmic process • regulation of circadian rhythm • regulation of apoptotic process • positive regulation of branching involved in ureteric bud morphogenesis • regulation of transcription from RNA polymerase II promoter • positive regulation of apoptotic signaling pathway • positive regulation of transcription, DNA-templated • negative regulation of epithelial cell proliferation • circadian regulation of gene expression • regulation of transcription, DNA-templated • positive regulation of MAP kinase activity • negative regulation of transcription, DNA-templated
Sources:Amigo / QuickGO
Orthologs
Species
Human
Mouse
Entrez
9500
94275
Ensembl
ENSG00000179222
ENSMUSG00000025151
UniProt
Q9Y5V3
Q9QYH6
RefSeq (mRNA)
NM_001005332 NM_001005333 NM_006986
NM_019791
RefSeq (protein)
NP_001005332 NP_001005333 NP_008917
NP_062765
Location (UCSC)
Chr X: 51.8 – 51.9 Mb
Chr X: 94.54 – 94.54 Mb
PubMed search
[3]
[4]
Wikidata
View/Edit Human
View/Edit Mouse
Melanoma-associated antigen D1 is a protein that in humans is encoded by the MAGED1 gene.[5][6]
Contents
1Function
2Interactions
3References
4Further reading
Function
This gene is a member of the melanoma antigen gene (MAGE) family. Most of the genes of this family encode tumor specific antigens that are not expressed in normal adult tissues except testis. Although the protein encoded by this gene shares strong homology with members of the MAGE family, it is expressed in almost all normal adult tissues. This gene has been demonstrated to be involved in the p75 neurotrophin receptor mediated programmed cell death pathway. Three transcript variants encoding two different isoforms have been found for this gene.[6]
MAGED was found to be deleted in a group of children with an intellectual disability disorder caused by a Xp11.22 deletion.[7]
Maged1 plays a role in controlling the reward circuitry in the brain of mice that is responsible for addictive behaviors.[8]
Interactions
MAGED1 has been shown to interact with UNC5A,[9]PJA1[10] and XIAP.[11]
References
^ abcGRCh38: Ensembl release 89: ENSG00000179222 - Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000025151 - Ensembl, May 2017
^"Human PubMed Reference:".
^"Mouse PubMed Reference:".
^Põld M, Zhou J, Chen GL, Hall JM, Vescio RA, Berenson JR (Sep 1999). "Identification of a new, unorthodox member of the MAGE gene family". Genomics. 59 (2): 161–7. doi:10.1006/geno.1999.5870. PMID 10409427.
^ ab"Entrez Gene: MAGED1 melanoma antigen family D, 1".
^Grau C, Starkovich M, Azamian MS, Xia F, Cheung SW, Evans P, Henderson A, Lalani SR, Scott DA (2017). "Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability". PLOS One. 12 (4): e0175962. doi:10.1371/journal.pone.0175962. PMC 5393878 . PMID 28414775.
^De Backer JF, Monlezun S, Detraux B, Gazan A, Vanopdenbosch L, Cheron J, et al. (July 2018). "Deletion of Maged1 in mice abolishes locomotor and reinforcing effects of cocaine". EMBO Reports. doi:10.15252/embr.201745089. PMID 30002119. Lay summary – ScienceDaily.
^Williams ME, Strickland P, Watanabe K, Hinck L (May 2003). "UNC5H1 induces apoptosis via its juxtamembrane region through an interaction with NRAGE". J. Biol. Chem. 278 (19): 17483–90. doi:10.1074/jbc.M300415200. PMID 12598531.
^Sasaki A, Masuda Y, Iwai K, Ikeda K, Watanabe K (Jun 2002). "A RING finger protein Praja1 regulates Dlx5-dependent transcription through its ubiquitin ligase activity for the Dlx/Msx-interacting MAGE/Necdin family protein, Dlxin-1". J. Biol. Chem. 277 (25): 22541–6. doi:10.1074/jbc.M109728200. PMID 11959851.
^Jordan BW, Dinev D, LeMellay V, Troppmair J, Gotz R, Wixler L, Sendtner M, Ludwig S, Rapp UR (Oct 2001). "Neurotrophin receptor-interacting mage homologue is an inducible inhibitor of apoptosis protein-interacting protein that augments cell death". J. Biol. Chem. 276 (43): 39985–9. doi:10.1074/jbc.C100171200. PMID 11546791.
Salehi AH, Roux PP, Kubu CJ, Zeindler C, Bhakar A, Tannis LL, Verdi JM, Barker PA (2000). "NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin receptor and facilitates nerve growth factor-dependent apoptosis". Neuron. 27 (2): 279–88. doi:10.1016/S0896-6273(00)00036-2. PMID 10985348.
Masuda Y, Sasaki A, Shibuya H, Ueno N, Ikeda K, Watanabe K (2001). "Dlxin-1, a novel protein that binds Dlx5 and regulates its transcriptional function". J. Biol. Chem. 276 (7): 5331–8. doi:10.1074/jbc.M008590200. PMID 11084035.
Kubu CJ, Goldhawk DG, Barker PA, Verdi JM (2001). "Identification of the translational initiation codon in human MAGED1". Genomics. 70 (1): 150–2. doi:10.1006/geno.2000.6356. PMID 11087672.
Zhang CG, Xing GC, Wei HD, Yu YT, He FC (2001). "[A new melanoma antigen-encoding gene subfamily in human chromosome X]". Yi Chuan Xue Bao. 28 (3): 197–203. PMID 11280991.
Stone B, Schummer M, Paley PJ, Crawford M, Ford M, Urban N, Nelson BH (2001). "MAGE-F1, a novel ubiquitously expressed member of the MAGE superfamily". Gene. 267 (2): 173–82. doi:10.1016/S0378-1119(01)00406-1. PMID 11313144.
Jordan BW, Dinev D, LeMellay V, Troppmair J, Gotz R, Wixler L, Sendtner M, Ludwig S, Rapp UR (2001). "Neurotrophin receptor-interacting mage homologue is an inducible inhibitor of apoptosis protein-interacting protein that augments cell death". J. Biol. Chem. 276 (43): 39985–9. doi:10.1074/jbc.C100171200. PMID 11546791.
Sasaki A, Masuda Y, Iwai K, Ikeda K, Watanabe K (2002). "A RING finger protein Praja1 regulates Dlx5-dependent transcription through its ubiquitin ligase activity for the Dlx/Msx-interacting MAGE/Necdin family protein, Dlxin-1". J. Biol. Chem. 277 (25): 22541–6. doi:10.1074/jbc.M109728200. PMID 11959851.
Xu YC, Wu RF, Gu Y, Yang YS, Yang MC, Nwariaku FE, Terada LS (2002). "Involvement of TRAF4 in oxidative activation of c-Jun N-terminal kinase". J. Biol. Chem. 277 (31): 28051–7. doi:10.1074/jbc.M202665200. PMID 12023963.
Kendall SE, Goldhawk DE, Kubu C, Barker PA, Verdi JM (2003). "Expression analysis of a novel p75(NTR) signaling protein, which regulates cell cycle progression and apoptosis". Mech. Dev. 117 (1–2): 187–200. doi:10.1016/S0925-4773(02)00204-6. PMID 12204258.
Williams ME, Strickland P, Watanabe K, Hinck L (2003). "UNC5H1 induces apoptosis via its juxtamembrane region through an interaction with NRAGE". J. Biol. Chem. 278 (19): 17483–90. doi:10.1074/jbc.M300415200. PMID 12598531.
Matsuda T, Suzuki H, Oishi I, Kani S, Kuroda Y, Komori T, Sasaki A, Watanabe K, Minami Y (2003). "The receptor tyrosine kinase Ror2 associates with the melanoma-associated antigen (MAGE) family protein Dlxin-1 and regulates its intracellular distribution". J. Biol. Chem. 278 (31): 29057–64. doi:10.1074/jbc.M302199200. PMID 12754255.
Wen CJ, Xue B, Qin WX, Yu M, Zhang MY, Zhao DH, Gao X, Gu JR, Li CJ (2004). "hNRAGE, a human neurotrophin receptor interacting MAGE homologue, regulates p53 transcriptional activity and inhibits cell proliferation". FEBS Lett. 564 (1–2): 171–6. doi:10.1016/S0014-5793(04)00353-9. PMID 15094062.
Bertrand M, Huijbers I, Chomez P, De Backer O (2005). "Comparative expression analysis of the MAGED genes during embryogenesis and brain development". Dev. Dyn. 230 (2): 325–34. doi:10.1002/dvdy.20026. PMID 15162511.
Tian XX, Rai D, Li J, Zou C, Bai Y, Wazer D, Band V, Gao Q (2005). "BRCA2 suppresses cell proliferation via stabilizing MAGE-D1". Cancer Res. 65 (11): 4747–53. doi:10.1158/0008-5472.CAN-05-0018. PMC 3295243 . PMID 15930293.
Xue B, Wen C, Shi Y, Zhao D, Li C (2005). "Human NRAGE disrupts E-cadherin/beta-catenin regulated homotypic cell-cell adhesion". Biochem. Biophys. Res. Commun. 336 (1): 247–51. doi:10.1016/j.bbrc.2005.08.069. PMID 16125672.
Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by expanding it.
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1 I having trouble getting my ResourceDictionary.MergedDictionaries to load from app.xaml. My WPF app has a static class with a Main defined and startup object set to it. Within Main I created an instance of App and run it. The override OnStartup fires and the mainwindow.cs InitializeComponent gives the error "Message "Cannot find resource named 'MaterialDesignFloatingActionMiniAccentButton'. If I put the resources in the mainwindow.xaml everything is fine, but I wanted them to load at the app level so I they are not in each page. Any help appreciated. public partial class App protected override void OnStartup(StartupEventArgs e) base.OnStartup(e); var app = new MainWindow(); var context = new MainWindowViewModel(); app.DataContext = context; app.Show(); from the Main.. var app = new App(); app.Run(); app.xaml.. <Application x:Class="GS.Server.App" xmlns="http://schemas.microsoft.com/winfx/2006/xaml/presentation" xmlns:...
up vote 2 down vote favorite There is a clear pattern that show for two separate subsets (set of columns); If one value is missing in a column, values of other columns in the same subset are missing for any row. Here is a visualization of missing data My tries up until now, I used ycimpute library to learn from other values, and applied Iterforest. I noted, score of Logistic regression is so weak (0.6) and thought Iterforest might not learn enough or anyway, except from outer subset which might not be enough? for example the subset with 11 columns might learn from the other columns but not from within it's members, and the same goes for the subset with four columns. This bar plot show better quantity of missings So of course, dealing with missings is better than dropping rows because It would affect my prediction which does contain the same missings quantity relatively. Any better way to deal with these ? [EDIT] The nullity pattern is confirmed: machine-learning cor...
. PMID 28414775. 
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