Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.
Open Access
- 1 December 1997
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 100 (11) , 2653-2657
- https://doi.org/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.Keywords
This publication has 20 references indexed in Scilit:
- Centre d'Etude du polymorphisme humain (CEPH): Collaborative genetic mapping of the human genomePublished by Elsevier ,2004
- Human Stanniocalcin Inhibits Renal Phosphate Excretion in the RatJournal of Bone and Mineral Research, 1997
- A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13.Genome Research, 1996
- Further Characterization of Proteins Associated with Elastic Fiber Microfibrils Including the Molecular Cloning of MAGP-2 (MP25)Journal of Biological Chemistry, 1996
- The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritanceNature Genetics, 1995
- Positional cloning moves from perditional to traditionalNature Genetics, 1995
- Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningoceleAmerican Journal of Medical Genetics, 1994
- A Microsatellite Genetic Linkage Map of Human Chromosome 18Genomics, 1993
- Complete structure of the human gene encoding neuron-specific enolaseGenomics, 1991
- Report of the committee on methods of linkage analysis and reportingCytogenetic and Genome Research, 1985