Evidence map›Paper›PMID 19700406›Full record

ReviewThe Journal of biological chemistry2009

Glucose-6-phosphatase catalytic subunit gene family.

John C Hutton, Richard M O'Brien

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
6.3field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

101 citing papers in PubMed, 206 citations in OpenAlex.

  1. Trial
  2. A FOXO1-G6PC transcriptional axis restrains renal cell carcinoma progression: multi-omics, epigenetic, and mechanistic evidence.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  3. Plants (Basel, Switzerland) · 2026
    Article
  4. Review
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  7. Review
  8. Computationally efficient whole-genome quantile regression at biobank scale.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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  18. Article
  19. Structural insights into glucose-6-phosphate recognition and hydrolysis by human G6PC1.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article

41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

John C HuttonBarbara Davis Center for Childhood Diabetes, University of Colorado at Denver, Aurora, Colorado 80045, USA.
Richard M O'Brien
University of Colorado Denver · USVanderbilt University · US

Funding

TRANSGENIC MOUSE/ ES CELL SHARES RESOURCESP60DK020593 · NIDDK · VANDERBILT UNIVERSITY · PI POWERS, ALVIN C · 1986 to 2011
$28.1M
UCHSC DIABETES ENDOCRINOLOGY RESEARCH CENTERP30DK057516 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI HUTTON, JOHN C · 2000 to 2010
$14.0M
MOLECULAR TARGETS OF CMI IN TYPE I DIABETESR01DK052068 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI DAVIDSON, HOWARD W · 1997 to 2014
$3.1M
REGULATION OF GLUCOSE-6-PHOSPHATASE GENE EXPRESSIONR01DK056374 · NIDDK · VANDERBILT UNIVERSITY · PI O'BRIEN, RICHARD M · 1999 to 2008
$2.9M
Regulation of IGRP Gene ExpressionR01DK061645 · NIDDK · VANDERBILT UNIVERSITY · PI O'BRIEN, RICHARD M · 2003 to 2007
$1.6M
The Role of IGRP in the Pathogenesis of Type 1 DiabetesR01DK076027 · NIDDK · VANDERBILT UNIVERSITY · PI O'BRIEN, RICHARD M · 2006 to 2010
$1.2M
Cloning of molecular targets of CMI in type 1 diabetesR56DK052068 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI DAVIDSON, HOWARD W, HUTTON, JOHN C · 2010 to 2010
$223k
NIDDK NIH HHS DK052068NIDDK NIH HHS DK076027NIDDK NIH HHS DK56374NIDDK NIH HHS DK61645NIDDK NIH HHS DK76027NIDDK NIH HHS P30 DK057516NIDDK NIH HHS P30 DK57516NIDDK NIH HHS P60 DK020593NIDDK NIH HHS P60 DK20593NIDDK NIH HHS R01 DK052068NIDDK NIH HHS R01 DK056374NIDDK NIH HHS R01 DK061645NIDDK NIH HHS R01 DK076027NIDDK NIH HHS R56 DK052068
6 · The paper itself

Abstract

Glucose-6-phosphatase catalyzes the hydrolysis of glucose 6-phosphate (G6P) to glucose and inorganic phosphate. It is a multicomponent system located in the endoplasmic reticulum that comprises several integral membrane proteins, namely a catalytic subunit (G6PC) and transporters for G6P, inorganic phosphate, and glucose. The G6PC gene family contains three members, designated G6PC, G6PC2, and G6PC3. The tissue-specific expression patterns of these genes differ, and mutations in all three genes have been linked to distinct diseases in humans. This minireview discusses the disease association and transcriptional regulation of the G6PC genes as well as the biological functions of the encoded proteins.

Indexed as

Gene Expression Regulation, EnzymologicMultigene FamilyMutationAnimalsCarbohydrate Metabolism, Inborn ErrorsCarrier ProteinsCatalytic DomainEndoplasmic ReticulumGlucose-6-PhosphataseHumansHydrolysisMultiprotein ComplexesOrgan SpecificityTranscription, GeneticCarrier ProteinsGlucose-6-PhosphataseMultiprotein Complexes

Identifiers

PMID19700406
PMCPMC2785553
OpenAlexW2081890649

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.