Journal article
Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3→p35
Diabetes (New York, N.Y.), Vol.36(4), pp.546-549
1987
DOI: 10.2337/diab.36.4.546
PMID: 3028891
Abstract
The glucose transporter is a membrane glycoprotein that is involved in the uptake of glucose by most, if not all, animal cells. A cloned cDNA that encodes the human protein was used to map the gene to a specific chromosomal region and to identify a DNA polymorphism. The human gene (designated GLUT) was assigned to chromosome 1p31.3----p35 by hybridization of the probe to DNA from a panel of human-mouse somatic cell hybrids containing different human chromosomes and by in situ hybridization to isolated metaphase chromosomes. The most likely location of GLUT is in 1p33. A common two-allele restriction-fragment-length polymorphism was identified with Xba I.
Details
- Title: Subtitle
- Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3→p35
- Creators
- Thomas B Shows - New York state dep. health, Roswell Park memorial inst., Buffalo NY 14263, United StatesRoger L Eddy - New York state dep. health, Roswell Park memorial inst., Buffalo NY 14263, United StatesMary G Byers - New York state dep. health, Roswell Park memorial inst., Buffalo NY 14263, United StatesYoshimitsu Fukushima - New York state dep. health, Roswell Park memorial inst., Buffalo NY 14263, United StatesCatherine R DeHaven - University of IowaJeffrey C Murray - University of IowaGraeme I Bell - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Diabetes (New York, N.Y.), Vol.36(4), pp.546-549
- DOI
- 10.2337/diab.36.4.546
- PMID
- 3028891
- NLM abbreviation
- Diabetes
- ISSN
- 0012-1797
- eISSN
- 1939-327X
- Publisher
- American Diabetes Association; Alexandria, VA
- Language
- English
- Date published
- 1987
- Academic Unit
- Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Dental Research
- Record Identifier
- 9984025691102771
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