<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Calonga-Solis V</submitter><pubmed_abstract>Even though immunoglobulins are critical for immune responses and human survival, the diversity of the immunoglobulin heavy chain gene (&lt;i>IGH&lt;/i>) is poorly known and mostly characterized only by serological methods. Moreover, this genomic region is not well-covered in genomic databases and genome-wide association studies due to particularities that impose technical difficulties for its analysis. Therefore, the &lt;i>IGH&lt;/i> gene has never been systematically sequenced across populations. Here, we deliver an unprecedented and comprehensive characterization of the diversity of the &lt;i>IGHG1, IGHG2&lt;/i>, and &lt;i>IGHG3&lt;/i> gene segments, which encode the constant region of the most abundant circulating immunoglobulins: IgG1, IgG2, and IgG3, respectively. We used Sanger sequencing to analyze 357 in</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1161</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6558194</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Unveiling the Diversity of Immunoglobulin Heavy Constant Gamma (&lt;i>IGHG&lt;/i>) Gene Segments in Brazilian Populations Reveals 28 Novel Alleles and Evidence of Gene Conversion and Natural Selection.</pubmed_title><pmcid>PMC6558194</pmcid><pubmed_authors>Calonga-Solis V</pubmed_authors><pubmed_authors>Vargas LB</pubmed_authors><pubmed_authors>Wassem R</pubmed_authors><pubmed_authors>Malheiros D</pubmed_authors><pubmed_authors>Augusto DG</pubmed_authors><pubmed_authors>Beltrame MH</pubmed_authors><pubmed_authors>Petzl-Erler ML</pubmed_authors><pubmed_authors>Issler HC</pubmed_authors><pubmed_authors>Dourado RM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Unveiling the Diversity of Immunoglobulin Heavy Constant Gamma (&lt;i>IGHG&lt;/i>) Gene Segments in Brazilian Populations Reveals 28 Novel Alleles and Evidence of Gene Conversion and Natural Selection.</name><description>Even though immunoglobulins are critical for immune responses and human survival, the diversity of the immunoglobulin heavy chain gene (&lt;i>IGH&lt;/i>) is poorly known and mostly characterized only by serological methods. Moreover, this genomic region is not well-covered in genomic databases and genome-wide association studies due to particularities that impose technical difficulties for its analysis. Therefore, the &lt;i>IGH&lt;/i> gene has never been systematically sequenced across populations. Here, we deliver an unprecedented and comprehensive characterization of the diversity of the &lt;i>IGHG1, IGHG2&lt;/i>, and &lt;i>IGHG3&lt;/i> gene segments, which encode the constant region of the most abundant circulating immunoglobulins: IgG1, IgG2, and IgG3, respectively. We used Sanger sequencing to analyze 357 in</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-04-29T03:43:14.396Z</modification><creation>2019-07-24T07:14:06Z</creation></dates><accession>S-EPMC6558194</accession><cross_references><pubmed>31214166</pubmed><doi>10.3389/fimmu.2019.01161</doi></cross_references></HashMap>