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614 lines
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81 KiB
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Accession: PRJNA31257 <span class="smallIndent" id="bioproject-acc" data-value="PRJNA31257">ID: 31257</span></div><div class="Title"><h2>Homo sapiens (human)</h2><h3>The Human Genome Project, currently maintained by the Genome Reference Consortium (GRC)</h3></div><div class="MainBody"><div class="Right"><div class="Genome ui-corner-all">See <a href="/genome/51" class="RegularLink">Genome</a> Information for Homo sapiens</div><div class="Navigate ui-corner-all"><div class="NavigateSectionHead">Navigate Across</div><div class="NavigateSection"><a class="RegularLink" href="/bioproject?term=9558[top+bioproject]+NOT+31257[uid]">99161 additional projects</a> are related by organism.</div></div></div><div class="Description"><div id="DescrHead">The human reference assembly defines a standard upon which other whole genome studies are based.<a class="RegularLinkB" href="javascript:void(0);" onclick="javascript:switchList('DescrHead','DescrAll');" title="Show whole description text"> More...</a></div><div id="DescrAll" style="display:none">The human reference assembly defines a standard upon which other whole genome studies are based. Providing the best representation of the human genome is essential for facilitating continued progress in understanding and improving human health.
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<p>The Human Genome Project (HGP) was an international research collaboration coordinated by the U.S. Department of Energy (DOE) and National Institutes of Health (NIH) whose goals were to determine the sequence of the human chromosomes and identify and map all human genes. The project began in 1988 when Congress funded both the NIH and the DOE and was completed in April of 2003. The HGP used a clone-oriented approach to produce map data, clone reagents, and the assembled human genome sequence. The International Human Genome Sequencing Consortium published the first draft of the human genome, with the sequence 90% complete, in the journal Nature in February 2001. The full sequence was completed in April 2003. The HGP resulted in significant technology, tool, and resource development that continues to have a significant impact on medicine and other life sciences. </p>
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<p>The Genome Reference Consortium (GRC) was formed in 2008 to maintain the reference assembly for the human genome. The goals of this group are to correct regions that are misrepresented, to close remaining gaps, and to produce alternative assemblies of structurally variant loci. The consortium does experimental work to address gaps or sub-optimal sequence regions and has developed the infrastructure to review and curate assembly joins. The GRC consists of: The Wellcome Trust Sanger Institute, The Genome Center at Washington University, The European Bioinformatics Institute and The National Center for Biotechnology Information. The public can see regions under review and report genome problems at the GRC website, <a href="http://genomereference.org" alt="link to GRC home page">http://genomereference.org</a>.
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</p>
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<p>The human genome assembly submitted by the GRC is available in GenBank under accession ranges GL000001-GL000258 (the scaffolds), and CM000663-CM000686 (the chromosomes).
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<a class="RegularLinkB" href="javascript:void(0);" onclick="javascript:switchList('DescrAll','DescrHead');" title="Collapse the text"> Less...</a></div></div><table id="CombinedTable"><tr><td class="CTtitle">Accession</td><td class="CTcontent">PRJNA31257</td></tr><tr><td class="CTtitle">Data Type</td><td class="CTcontent">Genome sequencing</td></tr><tr><td class="CTtitle">Scope</td><td class="CTcontent">Monoisolate</td></tr><tr><td class="CTtitle">Organism</td><td class="CTcontent"><a href="/taxonomy/9606" class="RegularLinkB" title="Homo sapiens in Taxonomy">Homo sapiens</a><span class="TID">[Taxonomy ID: 9606]</span><div class="CTLineage">Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens</div></td></tr><tr><td class="CTtitle">Publications (total 57) <a class="RegularLinkB" href="javascript:void(0);" id="LessPubEx" title="Collapse the publications list" style="display:none">Less...</a></td><td class="CTcontent"><div id="Pub1"><ul class="PubList"><li><a href="/pubmed/31593956" class="RegularLink">Fain JS <i>et al.,</i></a> "Epigenetic Coactivation of MAGEA6 and CT-GABRA3 Defines Orientation of a Segmental Duplication in the Human X Chromosome.", <i>Cytogenet Genome Res</i>, 2019;159(1):12-18</li></ul><a class="RegularLinkB" href="javascript:void(0);" id="MorePub" title="Show all publications">More...</a></div><div id="PubAll" style="display:none"><ul class="PubList "><li><a href="/pubmed/31593956" class="RegularLink">Fain JS <i>et al.,</i></a> "Epigenetic Coactivation of MAGEA6 and CT-GABRA3 Defines Orientation of a Segmental Duplication in the Human X Chromosome.", <i>Cytogenet Genome Res</i>, 2019;159(1):12-18</li><li><a href="/pubmed/27803192" class="RegularLink">Mohajeri K <i>et al.,</i></a> "Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region.", <i>Genome Res</i>, 2016 Nov;26(11):1453-1467</li><li><a href="/pubmed/25326701" class="RegularLink">Antonacci F <i>et al.,</i></a> "Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability.", <i>Nat Genet</i>, 2014 Dec;46(12):1293-302</li><li><a href="/pubmed/23932108" class="RegularLink">Genovese G <i>et al.,</i></a> "Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes.", <i>Am J Hum Genet</i>, 2013 Sep 5;93(3):411-21</li><li><a href="/pubmed/23872635" class="RegularLink">Mueller JL <i>et al.,</i></a> "Independent specialization of the human and mouse X chromosomes for the male germ line.", <i>Nat Genet</i>, 2013 Sep;45(9):1083-7</li><li><a href="/pubmed/23990606" class="RegularLink">Floutsakou I <i>et al.,</i></a> "The shared genomic architecture of human nucleolar organizer regions.", <i>Genome Res</i>, 2013 Dec;23(12):2003-12</li><li><a href="/pubmed/23541343" class="RegularLink">Watson CT <i>et al.,</i></a> "Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation.", <i>Am J Hum Genet</i>, 2013 Apr 4;92(4):530-46</li><li><a href="/pubmed/23435088" class="RegularLink">Genovese G <i>et al.,</i></a> "Using population admixture to help complete maps of the human genome.", <i>Nat Genet</i>, 2013 Apr;45(4):406-14, 414e1-2</li><li><a href="/pubmed/23042453" class="RegularLink">Falconer E <i>et al.,</i></a> "DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution.", <i>Nat Methods</i>, 2012 Nov;9(11):1107-12</li><li><a href="/pubmed/22482802" class="RegularLink">Itsara A <i>et al.,</i></a> "Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.", <i>Am J Hum Genet</i>, 2012 Apr 6;90(4):599-613</li><li><a href="/pubmed/20724583" class="RegularLink">Lemmers RJ <i>et al.,</i></a> "A unifying genetic model for facioscapulohumeral muscular dystrophy.", <i>Science</i>, 2010 Sep 24;329(5999):1650-3</li><li><a href="/pubmed/20729854" class="RegularLink">Antonacci F <i>et al.,</i></a> "A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.", <i>Nat Genet</i>, 2010 Sep;42(9):745-50</li><li><a href="/pubmed/20206332" class="RegularLink">Lemmers RJ <i>et al.,</i></a> "Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.", <i>Am J Hum Genet</i>, 2010 Mar 12;86(3):364-77</li><li><a href="/pubmed/20534489" class="RegularLink">Teague B <i>et al.,</i></a> "High-resolution human genome structure by single-molecule analysis.", <i>Proc Natl Acad Sci U S A</i>, 2010 Jun 15;107(24):10848-53</li><li><a href="/pubmed/21206914" class="RegularLink">Pyo CW <i>et al.,</i></a> "Different patterns of evolution in the centromeric and telomeric regions of group A and B haplotypes of the human killer cell Ig-like receptor locus.", <i>PLoS One</i>, 2010 Dec 29;5(12):e15115</li><li><a href="/pubmed/19490611" class="RegularLink">Garber M <i>et al.,</i></a> "Closing gaps in the human genome using sequencing by synthesis.", <i>Genome Biol</i>, 2009;10(6):R60</li><li><a href="/pubmed/20183526" class="RegularLink">Neafsey P <i>et al.,</i></a> "Genetic polymorphism in cytochrome P450 2D6 (CYP2D6): Population distribution of CYP2D6 activity.", <i>J Toxicol Environ Health B Crit Rev</i>, 2009;12(5-6):334-61</li><li><a href="/pubmed/18760392" class="RegularLink">Xue Y <i>et al.,</i></a> "Adaptive evolution of UGT2B17 copy-number variation.", <i>Am J Hum Genet</i>, 2008 Sep;83(3):337-46</li><li><a href="/pubmed/19165922" class="RegularLink">Zody MC <i>et al.,</i></a> "Evolutionary toggling of the MAPT 17q21.31 inversion region.", <i>Nat Genet</i>, 2008 Sep;40(9):1076-83</li><li><a href="/pubmed/18193213" class="RegularLink">Horton R <i>et al.,</i></a> "Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project.", <i>Immunogenetics</i>, 2008 Jan;60(1):1-18</li><li><a href="/pubmed/18674749" class="RegularLink">Young JM <i>et al.,</i></a> "Extensive copy-number variation of the human olfactory receptor gene family.", <i>Am J Hum Genet</i>, 2008 Aug;83(2):228-42</li><li><a href="/pubmed/18477386" class="RegularLink">Cole CG <i>et al.,</i></a> "Finishing the finished human chromosome 22 sequence.", <i>Genome Biol</i>, 2008;9(5):R78</li><li><a href="/pubmed/17924332" class="RegularLink">Lemmers RJ <i>et al.,</i></a> "Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.", <i>Am J Hum Genet</i>, 2007 Nov;81(5):884-94</li><li><a href="/pubmed/17367211" class="RegularLink">Zipfel PF <i>et al.,</i></a> "Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.", <i>PLoS Genet</i>, 2007 Mar 16;3(3):e41</li><li><a href="/pubmed/17573966" class="RegularLink">Makoff AJ <i>et al.,</i></a> "Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.", <i>Genome Biol</i>, 2007;8(6):R114</li><li><a href="/pubmed/16710414" class="RegularLink">Gregory SG <i>et al.,</i></a> "The DNA sequence and biological annotation of human chromosome 1.", <i>Nature</i>, 2006 May 18;441(7091):315-21</li><li><a href="/pubmed/16572171" class="RegularLink">Zody MC <i>et al.,</i></a> "Analysis of the DNA sequence and duplication history of human chromosome 15.", <i>Nature</i>, 2006 Mar 30;440(7084):671-5</li><li><a href="/pubmed/16554811" class="RegularLink">Taylor TD <i>et al.,</i></a> "Human chromosome 11 DNA sequence and analysis including novel gene identification.", <i>Nature</i>, 2006 Mar 23;440(7083):497-500</li><li><a href="/pubmed/16541075" class="RegularLink">Scherer SE <i>et al.,</i></a> "The finished DNA sequence of human chromosome 12.", <i>Nature</i>, 2006 Mar 16;440(7082):346-51</li><li><a href="/pubmed/16421571" class="RegularLink">Nusbaum C <i>et al.,</i></a> "DNA sequence and analysis of human chromosome 8.", <i>Nature</i>, 2006 Jan 19;439(7074):331-5</li><li><a href="/pubmed/16641997" class="RegularLink">Muzny DM <i>et al.,</i></a> "The DNA sequence, annotation and analysis of human chromosome 3.", <i>Nature</i>, 2006 Apr 27;440(7088):1194-8</li><li><a href="/pubmed/16625196" class="RegularLink">Zody MC <i>et al.,</i></a> "DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.", <i>Nature</i>, 2006 Apr 20;440(7087):1045-9</li><li><a href="/pubmed/16177791" class="RegularLink">Nusbaum C <i>et al.,</i></a> "DNA sequence and analysis of human chromosome 18.", <i>Nature</i>, 2005 Sep 22;437(7058):551-5</li><li><a href="/pubmed/15772651" class="RegularLink">Ross MT <i>et al.,</i></a> "The DNA sequence of the human X chromosome.", <i>Nature</i>, 2005 Mar 17;434(7031):325-37</li><li><a href="/pubmed/15653831" class="RegularLink">Kirsch S <i>et al.,</i></a> "Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome.", <i>Genome Res</i>, 2005 Feb;15(2):195-204</li><li><a href="/pubmed/16340004" class="RegularLink">Lewis SM <i>et al.,</i></a> "New approaches to the analysis of palindromic sequences from the human genome: evolution and polymorphism of an intronic site at the NF1 locus.", <i>Nucleic Acids Res</i>, 2005 Dec 9;33(22):e186</li><li><a href="/pubmed/15815621" class="RegularLink">Hillier LW <i>et al.,</i></a> "Generation and annotation of the DNA sequences of human chromosomes 2 and 4.", <i>Nature</i>, 2005 Apr 7;434(7034):724-31</li><li><a href="/pubmed/15372022" class="RegularLink">Schmutz J <i>et al.,</i></a> "The DNA sequence and comparative analysis of human chromosome 5.", <i>Nature</i>, 2004 Sep 16;431(7006):268-74</li><li><a href="/pubmed/15496913" class="RegularLink">International Human Genome Sequencing Consortium</a> "Finishing the euchromatic sequence of the human genome.", <i>Nature</i>, 2004 Oct 21;431(7011):931-45</li><li><a href="/pubmed/15164053" class="RegularLink">Humphray SJ <i>et al.,</i></a> "DNA sequence and analysis of human chromosome 9.", <i>Nature</i>, 2004 May 27;429(6990):369-74</li><li><a href="/pubmed/15164054" class="RegularLink">Deloukas P <i>et al.,</i></a> "The DNA sequence and comparative analysis of human chromosome 10.", <i>Nature</i>, 2004 May 27;429(6990):375-81</li><li><a href="/pubmed/14618296" class="RegularLink">Zanger UM <i>et al.,</i></a> "Cytochrome P450 2D6: overview and update on pharmacology, genetics, biochemistry.", <i>Naunyn Schmiedebergs Arch Pharmacol</i>, 2004 Jan;369(1):23-37</li><li><a href="/pubmed/15616553" class="RegularLink">Martin J <i>et al.,</i></a> "The sequence and analysis of duplication-rich human chromosome 16.", <i>Nature</i>, 2004 Dec 23;432(7020):988-94</li><li><a href="/pubmed/15057823" class="RegularLink">Dunham A <i>et al.,</i></a> "The DNA sequence and analysis of human chromosome 13.", <i>Nature</i>, 2004 Apr 1;428(6982):522-8</li><li><a href="/pubmed/15057824" class="RegularLink">Grimwood J <i>et al.,</i></a> "The DNA sequence and biology of human chromosome 19.", <i>Nature</i>, 2004 Apr 1;428(6982):529-35</li><li><a href="/pubmed/14574404" class="RegularLink">Mungall AJ <i>et al.,</i></a> "The DNA sequence and analysis of human chromosome 6.", <i>Nature</i>, 2003 Oct 23;425(6960):805-11</li><li><a href="/pubmed/12815422" class="RegularLink">Skaletsky H <i>et al.,</i></a> "The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.", <i>Nature</i>, 2003 Jun 19;423(6942):825-37</li><li><a href="/pubmed/12853948" class="RegularLink">Hillier LW <i>et al.,</i></a> "The DNA sequence of human chromosome 7.", <i>Nature</i>, 2003 Jul 10;424(6945):157-64</li><li><a href="/pubmed/12508121" class="RegularLink">Heilig R <i>et al.,</i></a> "The DNA sequence and analysis of human chromosome 14.", <i>Nature</i>, 2003 Feb 6;421(6923):601-7</li><li><a href="/pubmed/12355084" class="RegularLink">Lemmers RJ <i>et al.,</i></a> "Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.", <i>Nat Genet</i>, 2002 Oct;32(2):235-6</li><li><a href="/pubmed/11687796" class="RegularLink">Kuroda-Kawaguchi T <i>et al.,</i></a> "The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.", <i>Nat Genet</i>, 2001 Nov;29(3):279-86</li><li><a href="/pubmed/11237011" class="RegularLink">Lander ES <i>et al.,</i></a> "Initial sequencing and analysis of the human genome.", <i>Nature</i>, 2001 Feb 15;409(6822):860-921</li><li><a href="/pubmed/11780052" class="RegularLink">Deloukas P <i>et al.,</i></a> "The DNA sequence and comparative analysis of human chromosome 20.", <i>Nature</i>, 2001 Dec 20-27;414(6866):865-71</li><li><a href="/pubmed/10830953" class="RegularLink">Hattori M <i>et al.,</i></a> "The DNA sequence of human chromosome 21.", <i>Nature</i>, 2000 May 18;405(6784):311-9</li><li><a href="/pubmed/10508508" class="RegularLink">Andrews RM <i>et al.,</i></a> "Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.", <i>Nat Genet</i>, 1999 Oct;23(2):147</li><li><a href="/pubmed/10591208" class="RegularLink">Dunham I <i>et al.,</i></a> "The DNA sequence of human chromosome 22.", <i>Nature</i>, 1999 Dec 2;402(6761):489-95</li><li><a href="/pubmed/7219534" class="RegularLink">Anderson S <i>et al.,</i></a> "Sequence and organization of the human mitochondrial genome.", <i>Nature</i>, 1981 Apr 9;290(5806):457-65</li></ul><a class="RegularLinkB" href="javascript:void(0);" id="LessPub" title="Collapse the publications list">Less...</a></div></td></tr><tr><td class="CTtitle">Submission</td><td class="CTcontent">Registration date: 27-Feb-2009<br /><b><a href="/projects/genome/assembly/grc/" class="RegularLink">Genome Reference Consortium</a></b><br /><b><a href="http://www.genome.gov/11006939" class="RegularLink">International Human Genome Sequencing Consortium (IHGSC)</a></b><div class="Indent3"></div></td></tr><tr><td class="CTtitle">NCBI Links</td><td class="CTcontent"><ul class="LinksList"><li><a class="RegularLinkB" href="https://www.ncbi.nlm.nih.gov/projects/genome/assembly/grc/index.shtml" title="GRC" alt="GRC">GRC</a></li></ul></td></tr><tr><td class="CTtitle">Related Resources</td><td class="CTcontent"><ul class="LinksList"><li><a class="RegularLinkB" href="http://www.genome.gov/10001772" title="NHGRI" alt="NHGRI">NHGRI</a></li><li><a class="RegularLinkB" href="http://www.ornl.gov/sci/techresources/Human_Genome/home.shtml" title="DOE" alt="DOE">DOE</a></li></ul></td></tr></table><div class="Section SecTitle">Project Data:</div><div class="FrameGrid"><table class="FrameGrid" cellspacing="0" cellpadding="0"><tr><th class="RightIndent2 RB">Resource Name</th><th>Number<br />of Links</th></tr><tr><td colspan="2" class="DataGrp">Sequence data</td></tr><tr><td><span class="smallIndent">Nucleotide (Genomic DNA)</span></td><td class="alignRight"><a href="/sites/nuccore?term=31257[BioProject]" class="RegularLink" id="Nucleotide (Genomic DNA)">1012</a></td></tr><tr><td><span class="smallIndent">SRA Experiments</span></td><td class="alignRight"><a href="/sra?linkname=bioproject_sra_all&from_uid=31257" class="RegularLink" id="SRA Experiments">1</a></td></tr><tr><td><span class="smallIndent">Capillary Traces (Trace Archive)</span></td><td class="alignRight"><a href="/Traces/trace.cgi?cmd=retrieve&val=ncbi_project_id=31257" class="RegularLink" id="Capillary Traces (Trace Archive)">1</a></td></tr><tr><td colspan="2" class="DataGrp">Publications</td></tr><tr><td><span class="smallIndent">PubMed</span></td><td class="alignRight"><a href="/bioproject?Db=pubmed&DbFrom=bioproject&Cmd=Link&LinkName=bioproject_pubmed&LinkReadableName=PubMed&ordinalpos=1&IdsFromResult=31257" class="RegularLink" id="PubMed">57</a></td></tr><tr><td><span class="smallIndent">PMC</span></td><td class="alignRight"><a href="/bioproject?Db=pmc&DbFrom=bioproject&Cmd=Link&LinkName=bioproject_pmc&LinkReadableName=Full%20text%20in%20PMC&ordinalpos=1&IdsFromResult=31257" class="RegularLink" id="PMC">29</a></td></tr><tr><td colspan="2" class="DataGrp">Other datasets</td></tr><tr><td><span class="smallIndent">BioSample</span></td><td class="alignRight"><a href="/bioproject?Db=biosample&DbFrom=bioproject&Cmd=Link&LinkName=bioproject_biosample&LinkReadableName=BioSample&ordinalpos=1&IdsFromResult=31257" class="RegularLink" id="BioSample">1</a></td></tr><tr><td><span class="smallIndent">Assembly</span></td><td class="alignRight"><a href="/datasets/genome/?bioproject=PRJNA31257" class="RegularLink" id="Assembly">1</a></td></tr></table></div><div class="Frame100 ui-corner-all"><a class="jig-ncbitoggler-open RegularLink" toggles="ASetSec" title="Click to open/close the Assembly details table">Assembly details:</a><div class="relcontainer"><div id="ADdownload"><a class="RegularLinkB" title="Download Assembly details" href="#" pid="PRJNA31257">Download</a></div></div><div id="ASetSec" class="AggrAD"><div id="BSSet"><table id="AssemblyDetails" class="jig-ncbigrid" data-jigconfig="height: '20em'"><thead><tr><th title="Genome assembly organization and additional information">Assembly</th><th title="Assembly level">Level</th><th title="Chromosomes, organelles and plasmids">Chrs</th><th title="Taxonomy information">Taxonomy</th></tr></thead><tbody><tr><td><a class="RegularLink" href="/datasets/genome/GCA_000001405.29/" title="Genome assembly info">GCA_000001405.29</a></td><td nowrap="nowrap">Chromosome</td><td><div class="RightNum2"><a class="RegularLink" href="/nuccore/113200490,568336023,568336022,568336021,568336020,568336019,568336018,568336017,568336016,568336015,568336014,568336013,568336012,568336011,568336010,568336009,568336008,568336007,568336006,568336005,568336004,568336003,568336002,568336001,568336000" title="Chromosomes, organelles, plasmids associated with assembly GCA_000001405.29">25</a></div></td><td class="LeftNoWrap"><div class="smallIndent"><a class="RegularLink" href="/taxonomy/9606" title="Taxonomy information">Homo sapiens</a></div></td></tr></tbody></table></div></div></div><div class="Frame ui-corner-all"><a class="jig-ncbitoggler-open RegularLink" toggles="SRADataStat" title="Click to open/close SRA data details">SRA Data Details</a><div id="SRADataStat"><table class="jig-ncbigrid"><thead><tr><th class="RightIndent12">Parameter</th><th>Value</th></tr></thead><tbody><tr><td>Data volume, Mbytes</td><td>3</td></tr></tbody></table></div></div><div class="Aggr"><div class="TblTitle">Related RefSeq Project</div><div class="Indent3"><a href="/bioproject/168" class="RegularLink">PRJNA168</a> : RefSeq annotation of the human reference genome assembly</div></div></div></div></div>
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<h3>Related information</h3>
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<a class="brieflinkpopperctrl" href="/assembly?LinkName=bioproject_assembly_all&from_uid=31257" ref="log$=recordlinks">Assembly</a>
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<a class="brieflinkpopperctrl" href="/biosample?LinkName=bioproject_biosample_all&from_uid=31257" ref="log$=recordlinks">BioSample</a>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=bioproject_pmc&from_uid=31257" ref="log$=recordlinks">Full text in PMC</a>
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<a class="brieflinkpopperctrl" href="/genome?LinkName=bioproject_genome&from_uid=31257" ref="log$=recordlinks">Genome</a>
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<a class="brieflinkpopperctrl" href="/nuccore?LinkName=bioproject_nuccore&from_uid=31257" ref="log$=recordlinks">Nucleotide</a>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=bioproject_pubmed&from_uid=31257" ref="log$=recordlinks">PubMed</a>
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<div class="brieflinkpop offscreen_noflow">Genes related to a genome project</div>
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<a class="brieflinkpopperctrl" href="/sra?LinkName=bioproject_sra_all&from_uid=31257" ref="log$=recordlinks">SRA</a>
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<a class="brieflinkpopperctrl" href="https://www.ncbi.nlm.nih.gov/Traces/trace.cgi?cmd=retrieve&val=ncbi_project_id=31257" ref="log$=recordlinks">Traces</a>
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<h3>Related Resources</h3>
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<a class="brieflinkpopperctrl" href="https://gold.jgi.doe.gov/projects?id=Gp0038848" ref="itool=LinkOutPortlet&PrId=7663&uid=31257&db=bioproject&log$=linkoutlink">GOLD: Gp0038848</a>
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<span class="source">[Genomes On Line Database]</span>
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<a class="brieflinkpopperctrl" href="https://gold.jgi.doe.gov/projects?setColumns=yes&Project.NCBI+BioProject+Accession=PRJNA31257" ref="itool=LinkOutPortlet&PrId=7663&uid=31257&db=bioproject&log$=linkoutlink">GOLD: Gp0038848</a>
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<span class="source">[Genomes On Line Database]</span>
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<div class="ralinkpop offscreen_noflow">Homo sapiens<div class="brieflinkpopdesc">The Human Genome Project, currently maintained by the Genome Reference Consortium (GRC)</div></div>
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<div class="ralinkpop offscreen_noflow">RecName: Full=Histone demethylase UTY; AltName: Full=Ubiquitously-transcribed TPR protein on the Y chromosome; AltName: Full=Ubiquitously-transcribed Y chromosome tetratricopeptide repeat protein; AltName: Full=[histone H3]-trimethyl-L-lysine(27) demethylase UTY<div class="brieflinkpopdesc">gi|226693569|sp|O14607.2|UTY_HUMAN</div></div>
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<div class="ralinkpop offscreen_noflow">Homo sapiens ubiquitous TPR motif, Y isoform (UTY) mRNA, alternative transcript 1, complete cds<div class="brieflinkpopdesc">gi|2580577|gb|AF000996.1|HSAF000996</div></div>
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