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Journal article

Decreased STARD10 expression is associated with defective insulin secretion in humans and mice

Abstract:

Genetic variants near ARAP1 (CENTD2) and STARD10 influence type 2 diabetes (T2D) risk. The risk alleles impair glucose-induced insulin secretion and, paradoxically but characteristically, are associated with decreased proinsulin:insulin ratios, indicating improved proinsulin conversion. Neither the identity of the causal variants nor the gene(s) through which risk is conferred have been firmly established. Whereas ARAP1 encodes a GTPase activating protein, STARD10 is a member of the steroidog...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.ajhg.2017.01.011

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author
More from this funder
Grant:
095101/Z/10/Z
090532
098381
106130
National Institute for Health Research More from this funder
Publisher:
Cell Press Publisher's website
Journal:
American Journal of Human Genetics Journal website
Volume:
100
Issue:
2
Pages:
238–256
Publication date:
2017-01-26
Acceptance date:
2016-12-20
DOI:
EISSN:
1537-6605
ISSN:
0002-9297
Keywords:
Pubs id:
pubs:675460
UUID:
uuid:8c29a393-5faa-4169-a0f1-f4ebc59b0c5b
Local pid:
pubs:675460
Source identifiers:
675460
Deposit date:
2017-02-02

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