Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels

, , , McLaren, Gordon D., McLaren, Christine E., Chen, Wen Pin, Ramm, Louise E., Powell, Lawrie W., Ramm, Grant A., Barton, James C., & (2020) Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels. Blood Cells, Molecules, and Diseases, 85, Article number: 102463.

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Description

Glyceronephosphate O-acyltransferase (GNPAT) p.D519G (rs11558492) was identified as a genetic modifier correlated with more severe iron overload in hemochromatosis through whole-exome sequencing of HFE p.C282Y homozygotes with extreme iron phenotypes. We studied the prevalence of p.D519G in HFE p.C282Y/p.H63D compound heterozygotes, a genotype associated with iron overload in some patients. Cases were Australian participants with elevated serum ferritin (SF) levels ≥300μg/L (males) and ≥200μg/L (females); subjects whose SF levels were below these cut-offs were designated as controls. Samples were genotyped for GNPAT p.D519G. We compared the allele frequency of the present subjects, with/without elevated SF, to p.D519G frequency in public datasets. GNPAT p.D519G was more prevalent in our cohort of p.C282Y/p.H63D compound heterozygotes with elevated SF (37%) than European public datasets: 1000G 21%, gnomAD 20% and ESP 21%. We conclude that GNPAT p.D519G is associated with elevated SF in Australian HFE p.C282Y/p.H63D compound heterozygotes.

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1 citations in Web of Science®
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ID Code: 205185
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Wallace, Daniel F.orcid.org/0000-0002-6019-9424
Rishi, Gautamorcid.org/0000-0003-1022-2347
Subramaniam, V. Nathanorcid.org/0000-0002-4583-7790
Measurements or Duration: 5 pages
Additional URLs:
Keywords: Genetic modifiers, GNPAT, Hemochromatosis, HFE, Iron overload
DOI: 10.1016/j.bcmd.2020.102463
ISSN: 1079-9796
Pure ID: 68941972
Divisions: Current > Research Centres > Centre for Genomics and Personalised Health
Past > Institutes > Institute of Health and Biomedical Innovation
Current > QUT Faculties and Divisions > Faculty of Health
Funding Information: This work was supported by a Project Grant ( APP1082224 ) from the National Health and Medical Research Council (NHMRC) of Australia to VNS, DFW, and GAR. The work was also supported in part by Grant ( 1R24DK093433-01 ) from the National Institute of Diabetes and Digestive and Kidney Diseases , Grant ( P30 CA-62203 ) from the National Cancer Institute , and funds from the Department of Veterans Affairs . VNS is the recipient of an NHMRC Senior Research Fellowship ( APP1118888 ).
Copyright Owner: 2020 Elsevier Inc
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Deposited On: 06 Oct 2020 23:43
Last Modified: 14 Apr 2024 16:50