<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>47(4)</volume><submitter>Gassner C</submitter><pubmed_abstract>The U antigen (MNS5) is one of 49 antigens belonging to the MNS blood group system (ISBT002) carried on glycophorins A (GPA) and B (GPB). U is present on the red blood cells in almost all Europeans and Asians but absent in approximately 1.0% of Black Africans. U negativity coincides with negativity for S (MNS3) and s (MNS4) on GPB, thus be called S-s-U-, and is thought to arise from homozygous deletion of &lt;i>GYPB&lt;/i>. Little is known about the molecular background of these deletions. Bioinformatic analysis of the 1000 Genomes Project data revealed several candidate regions with apparent deletions in &lt;i>GYPB&lt;/i>. Highly specific Gap-PCRs, only resulting in positive amplification from DNAs with deletions present, allowed for the exact genetic localization of 3 different breakpoints; 110.24- </pubmed_abstract><journal>Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie</journal><pagination>326-336</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7443675</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Two Prevalent ∼100-kb &lt;i>GYPB&lt;/i> Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U- in Black Africans.</pubmed_title><pmcid>PMC7443675</pmcid><pubmed_authors>Just B</pubmed_authors><pubmed_authors>Trost N</pubmed_authors><pubmed_authors>Frey BM</pubmed_authors><pubmed_authors>Forster M</pubmed_authors><pubmed_authors>Franke A</pubmed_authors><pubmed_authors>Bensing KM</pubmed_authors><pubmed_authors>Storry JR</pubmed_authors><pubmed_authors>Gassner C</pubmed_authors><pubmed_authors>Meyer S</pubmed_authors><pubmed_authors>Engstrom C</pubmed_authors><pubmed_authors>Denomme GA</pubmed_authors><pubmed_authors>Song YL</pubmed_authors><pubmed_authors>Jungbauer C</pubmed_authors><pubmed_authors>Portmann C</pubmed_authors><pubmed_authors>Mattle-Greminger MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Two Prevalent ∼100-kb &lt;i>GYPB&lt;/i> Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S-s-U- in Black Africans.</name><description>The U antigen (MNS5) is one of 49 antigens belonging to the MNS blood group system (ISBT002) carried on glycophorins A (GPA) and B (GPB). U is present on the red blood cells in almost all Europeans and Asians but absent in approximately 1.0% of Black Africans. U negativity coincides with negativity for S (MNS3) and s (MNS4) on GPB, thus be called S-s-U-, and is thought to arise from homozygous deletion of &lt;i>GYPB&lt;/i>. Little is known about the molecular background of these deletions. Bioinformatic analysis of the 1000 Genomes Project data revealed several candidate regions with apparent deletions in &lt;i>GYPB&lt;/i>. Highly specific Gap-PCRs, only resulting in positive amplification from DNAs with deletions present, allowed for the exact genetic localization of 3 different breakpoints; 110.24- </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2026-06-02T16:17:55.383Z</modification><creation>2020-09-05T07:09:35Z</creation></dates><accession>S-EPMC7443675</accession><cross_references><pubmed>32884505</pubmed><doi>10.1159/000504946</doi></cross_references></HashMap>