<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>94(4)</volume><submitter>Mizuki N</submitter><pubmed_abstract>A member of a novel family of the human major histocompatibility complex (MHC) class I genes termed MIC (MHC class I chain-related genes), MICA, has been recently identified near the HLA-B gene on the short arm of human chromosome 6. The predicted amino acid sequence of the MICA chain suggests that it folds similarly to typical class I chains and may have the capacity to bind peptides or other short ligands. Therefore, MICA is predicted to have a specialized function in antigen presentation or T cell recognition. During nucleotide sequence analyses of the MICA genomic clone, we found a triplet repeat microsatellite polymorphism of (GCT/AGC)n in the transmembrane (TM) region of the MICA gene. In 68 HLA homozygous B cell lines, 5 distinct alleles of this microsatellite sequence were detected</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>1298-303</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC19785</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association of six GCT repetitions with Behcet disease.</pubmed_title><pmcid>PMC19785</pmcid><pubmed_authors>Ohno S</pubmed_authors><pubmed_authors>Goto K</pubmed_authors><pubmed_authors>Yamazaki M</pubmed_authors><pubmed_authors>Ota M</pubmed_authors><pubmed_authors>Ando H</pubmed_authors><pubmed_authors>Mizuki N</pubmed_authors><pubmed_authors>Watanabe K</pubmed_authors><pubmed_authors>Inoko H</pubmed_authors><pubmed_authors>Nakamura S</pubmed_authors><pubmed_authors>Kimura M</pubmed_authors><pubmed_authors>Katsuyama Y</pubmed_authors><pubmed_authors>Bahram S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association of six GCT repetitions with Behcet disease.</name><description>A member of a novel family of the human major histocompatibility complex (MHC) class I genes termed MIC (MHC class I chain-related genes), MICA, has been recently identified near the HLA-B gene on the short arm of human chromosome 6. The predicted amino acid sequence of the MICA chain suggests that it folds similarly to typical class I chains and may have the capacity to bind peptides or other short ligands. Therefore, MICA is predicted to have a specialized function in antigen presentation or T cell recognition. During nucleotide sequence analyses of the MICA genomic clone, we found a triplet repeat microsatellite polymorphism of (GCT/AGC)n in the transmembrane (TM) region of the MICA gene. In 68 HLA homozygous B cell lines, 5 distinct alleles of this microsatellite sequence were detected</description><dates><release>1997-01-01T00:00:00Z</release><publication>1997 Feb</publication><modification>2025-04-04T09:42:59.367Z</modification><creation>2019-03-26T23:45:22Z</creation></dates><accession>S-EPMC19785</accession><cross_references><pubmed>9037047</pubmed><doi>10.1073/pnas.94.4.1298</doi></cross_references></HashMap>