Title | Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Rosenthal, EA, Makaryan, V, Burt, AA, Crosslin, DR, Kim, DSeung, Smith, JD, Nickerson, DA, Reiner, AP, Rich, SS, Jackson, RD, Ganesh, SK, Polfus, LM, Qi, L, Dale, DC, Jarvik, GP |
Corporate Authors | University of Washington, Center for Mendelian Genomics |
Journal | Genet Epidemiol |
Volume | 40 |
Issue | 6 |
Pagination | 470-4 |
Date Published | 2016 09 |
ISSN | 1098-2272 |
Keywords | Adult, Aged, Aged, 80 and over, Alleles, Cohort Studies, Female, Gene Frequency, Genotype, High-Throughput Nucleotide Sequencing, Humans, Leukocyte Count, Male, Middle Aged, Mutation, Missense, National Heart, Lung, and Blood Institute (U.S.), Neutropenia, Neutrophils, Sequence Analysis, DNA, United States, Vacuolar Proton-Translocating ATPases |
Abstract | Neutrophils are a key component of innate immunity. Individuals with low neutrophil count are susceptible to frequent infections. Linkage and association between congenital neutropenia and a single rare missense variant in TCIRG1 have been reported in a single family. Here, we report on nine rare missense variants at evolutionarily conserved sites in TCIRG1 that are associated with lower absolute neutrophil count (ANC; p = 0.005) in 1,058 participants from three cohorts: Atherosclerosis Risk in Communities (ARIC), Coronary Artery Risk Development in Young Adults (CARDIA), and Jackson Heart Study (JHS) of the NHLBI Grand Opportunity Exome Sequencing Project (GO ESP). These results validate the effects of TCIRG1 coding variation on ANC and suggest that this gene may be associated with a spectrum of mild to severe effects on ANC. |
DOI | 10.1002/gepi.21976 |
Alternate Journal | Genet. Epidemiol. |
PubMed ID | 27229898 |
PubMed Central ID | PMC5079157 |
Grant List | RC2 HL102923 / HL / NHLBI NIH HHS / United States R24 AI049393 / AI / NIAID NIH HHS / United States RC2 HL102926 / HL / NHLBI NIH HHS / United States U01 HG008657 / HG / NHGRI NIH HHS / United States RC2 HL102924 / HL / NHLBI NIH HHS / United States UM1 HG006493 / HG / NHGRI NIH HHS / United States RC2 HL103010 / HL / NHLBI NIH HHS / United States RC2 HL102925 / HL / NHLBI NIH HHS / United States |