Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.

Genomics - 1 Sept 1993

Turk E, Klisak I, Bacallao R, Sparkes R S, Wright E M

Abstract excerpt

The Na+/glucose cotransporter gene SGLT1 encodes the primary carrier protein responsible for the uptake of the dietary sugars glucose and galactose from the intestinal lumen. SGLT1 transport activity is currently exploited in oral rehydration therapy. The 75-kDa glycoprotein is localized in the brush border of the intestinal epithelium and is predicted to comprise 12 membrane spans. In two patients with the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carrier Proteins
Share to Chromosome Banding
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cosmids

Share to In Situ Hybridization, Fluorescence

Share to Membrane Glycoproteins

Share to Membrane Proteins

Share to Mutation

Source

Identifiers

PMID: 8244393
DOI: 10.1006/geno.1993.1399

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Assignment of the human Na+/glucose cotransporter gene SGLT1 to chromosome 22q13.1.PMID 8244393Read ↗

Structure of the human Na+/glucose cotransporter gene SGLT1.Semantic proximity Read ↗

Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.Semantic proximity Read ↗

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.Semantic proximity Read ↗

Localization of the Na+/Glucose Cotransporter Gene SGLT2 to Human Chromosome 16 Close to the CentromereSemantic proximity Read ↗

Molecular basis for glucose-galactose malabsorption.Semantic proximity Read ↗

SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.Semantic proximity Read ↗

Molecular cloning of a member of the facilitative glucose transporter gene family GLUT11 (SLC2A11) and identification of transcription variants.Semantic proximity Read ↗

A missense mutation in the Na+/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant proteinSemantic proximity Read ↗

Novel and Unexpected Functions of SGLTsSemantic proximity Read ↗

Mapping the human liver/islet glucose transporter (GLUT2) gene within a genetic linkage map of chromosome 3q using a (CA)n dinucleotide repeat polymorphism and characterization of the polymorphism in three racial groups.Semantic proximity Read ↗

Identification of a disulfide bridge linking the fourth and the seventh extracellular loops of the Na+/glucose cotransporter.Semantic proximity Read ↗

Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.