Citations for
1MRXS30, UBE2A
A novel UBE2A mutation causes X-linked intellectual disability type Nascimento.
Tsurusaki Y, Ohashi I, Enomoto Y, Naruto T, Mitsui J, Aida N, Kurosawa K.
Hum Genome Var 4:17019. doi: 10.1038/hgv.2017.19. eCollection 2017. 2017
2RNF20, UBE2A, WDR76
Subnuclear Relocalization of Structure-Specific Endonucleases in Response to DNA Damage.
Saugar I, Jiménez-Martín A, Tercero JA.
Cell Rep 20(7):1553-1562. doi: 10.1016/j.celrep.2017.07.059. 2017
3UBE2A
An essential role for UBE2A/HR6A in learning and memory and mGLUR-dependent long-term depression.
Bruinsma CF, Savelberg SM, Kool MJ, Jolfaei MA, Van Woerden GM, Baarends WM, Elgersma Y.
Hum Mol Genet 25(1):1-8. doi: 10.1093/hmg/ddv436. Epub 2015 Oct 16. 2016
4CBX5, UBE2A
RAD6 promotes homologous recombination repair by activating the autophagy-mediated degradation of heterochromatin protein HP1.
Chen S, Wang C, Sun L, Wang DL, Chen L, Huang Z, Yang Q, Gao J, Yang XB, Chang JF, Chen P, Lan L, Mao Z, Sun FL.
Mol Cell Biol 35(2):406-16. doi: 10.1128/MCB.01044-14. Epub 2014 Nov 10. 2015
5ASF1A, MDM2, UBE2A, UBE2B
A conserved RAD6-MDM2 ubiquitin ligase machinery targets histone chaperone ASF1A in tumorigenesis.
Wang C, Chang JF, Yan H, Wang DL, Liu Y, Jing Y, Zhang M, Men YL, Lu D, Yang XM, Chen S, Sun FL.
Oncotarget 6(30):29599-613. doi: 10.18632/oncotarget.5011. 2015
6MRXS30, UBE2A
UBE2A deficiency syndrome: a report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene.
Thunstrom S, Sodermark L, Ivarsson L, Samuelsson L, Stefanova M.
Am J Med Genet A 167A(1):204-10. doi: 10.1002/ajmg.a.36800. Epub 2014 Oct 6. 2015
7UBE2A
Human RAD6 promotes G1-S transition and cell proliferation through upregulation of cyclin D1 expression.
Cai F, Chen P, Chen L, Biskup E, Liu Y, Chen PC, Chang JF, Jiang W, Jing Y, Chen Y, Jin H, Chen S.
PLoS One 9(11):e113727. doi: 10.1371/journal.pone.0113727. eCollection 2014. 2014
8RNF168, UBE2A, UBE2B
RNF168 forms a functional complex with RAD6 during the DNA damage response.
Liu C, Wang D, Wu J, Keller J, Ma T, Yu X.
J Cell Sci 126(Pt 9):2042-51. doi: 10.1242/jcs.122945. Epub 2013 Mar 22. 2013
9UBE2A
Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy.
Haddad DM, Vilain S, Vos M, Esposito G, Matta S, Kalscheuer VM, Craessaerts K, Leyssen M, Nascimento RM, Vianna-Morgante AM, De Strooper B, Van Esch H, Morais VA, Verstreken P.
Mol Cell 50(6):831-43. doi: 10.1016/j.molcel.2013.04.012. Epub 2013 May 16. 2013
10UBE2A, UBE2B
RAD6 regulates the dosage of p53 by a combination of transcriptional and posttranscriptional mechanisms.
Chen S, Wang DL, Liu Y, Zhao L, Sun FL.
Mol Cell Biol 32(2):576-87. doi: 10.1128/MCB.05966-11. Epub 2011 Nov 14. 2012
11DELXQM, MRXS30, UBE2A
Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.
Honda S, Orii KO, Kobayashi J, Hayashi S, Imamura A, Imoto I, Nakagawa E, Goto Y, Inazawa J.
J Hum Genet 55(4):244-7. Epub 2010 Mar 26. 2010
12MRXS30, UBE2A
Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndrome.
Budny B, Badura-Stronka M, Materna-Kiryluk A, Tzschach A, Raynaud M, Latos-Bielenska A, Ropers HH.
Clin Genet 77(6):541-51. Epub 2010 Apr 19.PMID: 20412111 2010
13HIST2H2BE, RNF20, UBE2A
RAD6-Mediated transcription-coupled H2B ubiquitylation directly stimulates H3K4 methylation in human cells.
Kim J, Guermah M, McGinty RK, Lee JS, Tang Z, Milne TA, Shilatifard A, Muir TW, Roeder RG.
Cell 137(3):459-71.PMID: 19410543 2009
14HLTF, UBE2V2, UBE2A, UBE2B, RAD18, UBE2N
Human HLTF functions as a ubiquitin ligase for proliferating cell nuclear antigen polyubiquitination.
Unk I, Hajdś I, F‡tyol K, Hurwitz J, Yoon JH, Prakash L, Prakash S, Haracska L.
Proc Natl Acad Sci U S A 105(10):3768-73. Epub 2008 Mar 3. 2008
15UBE2A
Ubiquitin conjugating enzymes participate in polyglutamine protein aggregation.
Howard RA, Sharma P, Hajjar C, Caldwell KA, Caldwell GA, du Breuil R, Moore R, Boyd L.
BMC Cell Biol 8:32.PMID: 17663792 2007
16UBE2A, UBE2B
Functional characterization of Rad18 domains for Rad6, ubiquitin, DNA binding and PCNA modification.
Notenboom V, Hibbert RG, van Rossum-Fikkert SE, Olsen JV, Mann M, Sixma TK.
Nucleic Acids Res 35(17):5819-30. Epub 2007 Aug 24. 2007
17UBE2A, MRXS30
UBE2A, Which Encodes a Ubiquitin-Conjugating Enzyme, Is Mutated in a Novel X-Linked Mental Retardation Syndrome.
Nascimento RM, Otto PA, de Brouwer AP, Vianna-Morgante AM.
Am J Hum Genet 79(3):549-55. Epub 2006 Jul 3. 2006
18HIST2H2BE, RNF20, UBE2A
Histone H2B ubiquitylation is associated with elongating RNA polymerase II.
Xiao T, Kao CF, Krogan NJ, Sun ZW, Greenblatt JF, Osley MA, Strahl BD.
Mol Cell Biol 25(2):637-51.PMID: 15632065 2005
19UBE2A, UBE2B, RAD18, ZMYM2
ZNF198 protein, involved in rearrangement in myeloproliferative disease, forms complexes with the DNA repair-associated HHR6A/6B and RAD18 proteins.
Kunapuli P, Somerville R, Still IH, Cowell JK.
Oncogene 22(22):3417-23. 2003
20UBE2A, UBE2B
Localization of two human homologs, HHR6A and HHR6B, of the yeast DNA repair gene RAD6 to chromosomes Xq24-q25 and 5q23-q31.
Koken MHM, et al.
Genomics 12 : 447-453. 1992
21UBE2A, UBE2B
cDNA cloning of a novel human ubiquitin carrier protein.
Liu Z, et al.
J Biol Chem 267 : 15829-15835. 1992
22UBE2A, UBE2B
Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6.
Koken MH, et al.
Proc Natl Acad Sci U S A 88 : 8865-8869. 1991