<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(6)</volume><submitter>Lei H</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Mutations of the ABO gene may cause the dysfunction of ABO glycosyltransferase (GT) that can result in weak ABO phenotypes. Here, we identified two novel weak ABO subgroup alleles and explored their mechanisms that caused A&lt;sub>el&lt;/sub> and B&lt;sub>el&lt;/sub> phenotypes.&lt;h4>Materials and methods&lt;/h4>The ABO phenotyping and genotyping were performed by serological studies and direct DNA sequencing of the ABO gene. The role of the novel mutations were evaluated by a three-dimensional model, predicting protein structure changes, and in vitro expression assay. The total glycosyltransferase transfer capacity in supernatant of transfected cells was examined.&lt;h4>Results&lt;/h4>We identified a mutation c. 955C>G (p. L319V) of A allele in an A&lt;sub>el&lt;/sub> subject and a mutation c. 272T</pubmed_abstract><journal>Blood transfusion = Trasfusione del sangue</journal><pagination>471-477</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7605879</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A&lt;sub>el&lt;/sub> and B&lt;sub>el&lt;/sub> phenotypes.</pubmed_title><pmcid>PMC7605879</pmcid><pubmed_authors>Lei H</pubmed_authors><pubmed_authors>Xiang D</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Cai X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A&lt;sub>el&lt;/sub> and B&lt;sub>el&lt;/sub> phenotypes.</name><description>&lt;h4>Background&lt;/h4>Mutations of the ABO gene may cause the dysfunction of ABO glycosyltransferase (GT) that can result in weak ABO phenotypes. Here, we identified two novel weak ABO subgroup alleles and explored their mechanisms that caused A&lt;sub>el&lt;/sub> and B&lt;sub>el&lt;/sub> phenotypes.&lt;h4>Materials and methods&lt;/h4>The ABO phenotyping and genotyping were performed by serological studies and direct DNA sequencing of the ABO gene. The role of the novel mutations were evaluated by a three-dimensional model, predicting protein structure changes, and in vitro expression assay. The total glycosyltransferase transfer capacity in supernatant of transfected cells was examined.&lt;h4>Results&lt;/h4>We identified a mutation c. 955C>G (p. L319V) of A allele in an A&lt;sub>el&lt;/sub> subject and a mutation c. 272T</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2025-04-04T22:26:32.202Z</modification><creation>2020-11-19T16:13:05Z</creation></dates><accession>S-EPMC7605879</accession><cross_references><pubmed>32281923</pubmed><doi>10.2450/2020.008-20</doi></cross_references></HashMap>