Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21

descriptionPublicationkeyboard_double_arrow_right Article 01 Dec 1986 English Publisher:Springer Science and Business Media LLCJournal:Human Genetics, volume 74, pages 420-422 (issn: 0340-6717, eissn: 1432-1203,

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Authors: M G, Mattei; Y, Colin; C, Le Van Kim; J F, Mattei; J P, Cartron;

doi: 10.1007/bf00280497

pmid: 3793105

Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21

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Abstract

A complementary cDNA clone (900 bp) representing the 3' untranslated region and almost the entire coding sequence of the human erythrocyte membrane glycophorin C has been used to determine the chromosomal location of the blood group Gerbich locus by in situ hybridization. The results indicate that this locus is assigned to the region q14-q21 of chromosome 2.

Related Organizations

Centre Hospitalier Universitaire de Toulouse
France
Hôpital des Enfants
France
Centre de Génétique Médicale de Marseille
France
French Institute of Health and Medical Research
France

Keywords

Chromosomes, Human, Pair 2, Karyotyping, Sialoglycoproteins, Chromosome Mapping, Humans, Nucleic Acid Hybridization, DNA, Glycophorins, Chromosome Banding

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