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常染色体显性低磷性佝偻病与12号染色体短臂13区相关联。

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

作者信息

Econs M J, McEnery P T, Lennon F, Speer M C

机构信息

Department of Medicine, Duke University Medical Center and the Durham Veterans Affairs Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Clin Invest. 1997 Dec 1;100(11):2653-7. doi: 10.1172/JCI119809.

Abstract

Autosomal dominant hypophosphatemic rickets (ADHR) is an inherited disorder of isolated renal phosphate wasting, the pathogenesis of which is unknown. We performed a genome-wide linkage study in a large kindred to determine the chromosome location of the ADHR gene. Two-point LOD scores indicate that the gene is linked to the markers D12S314 [Z(theta) = 3.15 at theta = 0.0], vWf [Z(theta) = 5.32 at theta = 0.0], and CD4 [Z(theta) = 3.53 at theta = 0.0]. Moreover, multilocus analysis indicates that the ADHR gene locus is located on chromosome 12p13 in the 18-cM interval between the flanking markers D12S100 and D12S397. These data are the first to establish a chromosomal location for the ADHR locus and to provide a framework map to further localize the gene. Such studies will permit ultimate identification of the ADHR gene and provide further insight into phosphate homeostasis.

摘要

常染色体显性低磷性佝偻病(ADHR)是一种孤立性肾性磷酸盐流失的遗传性疾病,其发病机制尚不清楚。我们在一个大家系中进行了全基因组连锁研究,以确定ADHR基因的染色体定位。两点连锁分析得分表明该基因与标记D12S314(在θ = 0.0时,Z(θ) = 3.15)、vWf(在θ = 0.0时,Z(θ) = 5.32)和CD4(在θ = 0.0时,Z(θ) = 3.53)连锁。此外,多位点分析表明ADHR基因座位于12号染色体p13区,在侧翼标记D12S100和D12S397之间18厘摩的区间内。这些数据首次确定了ADHR基因座的染色体定位,并提供了一个框架图谱以进一步定位该基因。此类研究将最终鉴定出ADHR基因,并为磷酸盐稳态提供更深入的见解。

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