Literature DB >> 9428641

Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.

I Gerin1, M Veiga-da-Cunha, Y Achouri, J F Collet, E Van Schaftingen.   

Abstract

We report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologous to bacterial transporters for phosphate esters. This protein presents at its carboxy terminus the consensus motif for retention in the endoplasmic reticulum. Northern blots of rat tissues indicate that the corresponding mRNA is mostly expressed in liver and kidney. In two patients with glycogen storage disease type Ib, mutations were observed that either replaced a conserved Gly to Cys or introduced a premature stop codon. The encoded protein is therefore most likely the glucose 6-phosphate translocase that is functionally associated with glucose-6-phosphatase.

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Year:  1997        PMID: 9428641     DOI: 10.1016/s0014-5793(97)01463-4

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  43 in total

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Review 3.  Hepatic glucose sensing and integrative pathways in the liver.

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Review 5.  Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease.

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Journal:  Hum Mutat       Date:  2008-07       Impact factor: 4.878

Review 6.  Specific features of glycogen metabolism in the liver.

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8.  Identification of protein components of the microsomal glucose 6-phosphate transporter by photoaffinity labelling.

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Review 9.  Genetic heterogeneity in severe congenital neutropenia: how many aberrant pathways can kill a neutrophil?

Authors:  Alejandro A Schäffer; Christoph Klein
Journal:  Curr Opin Allergy Clin Immunol       Date:  2007-12

10.  Immunodetection of the expression of microsomal proteins encoded by the glucose 6-phosphate transporter gene.

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