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Publication : Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ).

First Author  Hayasaka K Year  1993
Journal  Genomics Volume  17
Issue  3 Pages  755-8
PubMed ID  7503936 Mgi Jnum  J:14536
Mgi Id  MGI:62701 Doi  10.1006/geno.1993.1400
Citation  Hayasaka K, et al. (1993) Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ). Genomics 17(3):755-8
abstractText  We describe the cloning, characterization, and chromosomal mapping of the human myelin protein zero (MPZ) gene. The gene is about 7 kb long and consists of six exons corresponding to the functional domains. All exon-intron junction sequences conform to the GT/AG rule. The 5'-flanking region of the gene has a TA-rich element (TATA-like box), two CAAT boxes, and a single defined transcription initiation site detected by the primer extension method. The gene for human MPZ was assigned to chromosome 1q22-q23 by spot blot hybridization of flow-sorted human chromosomes and fluorescence in situ hybridization. The localization of the MPZ gene coincides with the locus for Charcot-Marie-Tooth disease type 1B, determined by linkage analysis.
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