Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders.

Abstract:

:On the basis of studies with animal models, the gene for the low-affinity receptor for immunoglobulin E (IgE) (FCER2, CD23) has been implicated as a candidate for IgE-mediated allergic diseases and bronchial hyperreactivity, or related traits. Given evidence for genetic complexity in atopic disorders, we sought to study two European subpopulations, Finnish and Catalonian. We studied three phenotypic markers: (1) total serum IgE level; (2) asthma; and (3) specific IgE level for a mixture of the most common aeroallergens in Finland. Altogether, eight polymorphic markers spanning a region of 10 cM around the FCER2 gene on chromosome 19p13 were analyzed in 124 families. The physical order of the markers and the location of the FCER2 gene were confirmed by using radiation hybrids. The allele and haplotype association study showed a suggestive haplotype association (significance of p

authors

Laitinen T,Ollikainen V,Lázaro C,Kauppi P,de Cid R,Antó JM,Estivill X,Lokki H,Mannila H,Laitinen LA,Kere J

doi

10.1164/ajrccm.161.3.9810056

keywords:

subject

Has Abstract

pub_date

2000-03-01 00:00:00

pages

700-6

issue

3 Pt 1

eissn

1073-449X

issn

1535-4970

journal_volume

161

pub_type

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