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J Clin Invest. 1997 Dec 1; 100(11): 2653–2657.
PMCID: PMC508467
PMID: 9389727

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

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.

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Selected References

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  • Econs MJ, McEnery PT. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder. J Clin Endocrinol Metab. 1997 Feb;82(2):674–681. [PubMed] [Google Scholar]
  • GREENBERG BG, WINTERS RW, GRAHAM JB. The normal range of serum inorganic phosphorus and its utility as a discriminant in the diagnosis of congenital hypophosphatemia. J Clin Endocrinol Metab. 1960 Mar;20:364–379. [PubMed] [Google Scholar]
  • Econs MJ, Barker DF, Speer MC, Pericak-Vance MA, Fain PR, Drezner MK. Multilocus mapping of the X-linked hypophosphatemic rickets gene. J Clin Endocrinol Metab. 1992 Jul;75(1):201–206. [PubMed] [Google Scholar]
  • O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet. 1995 Dec;11(4):402–408. [PubMed] [Google Scholar]
  • Chatkupt S, Speer MC, Ding Y, Thomas M, Stenroos ES, Dermody JJ, Koenigsberger MR, Ott J, Johnson WG. Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. Am J Med Genet. 1994 Aug 1;52(1):1–4. [PubMed] [Google Scholar]
  • Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R. Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet. 1985;40(1-4):356–359. [PubMed] [Google Scholar]
  • Ploughman LM, Boehnke M. Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet. 1989 Apr;44(4):543–551. [PMC free article] [PubMed] [Google Scholar]
  • Dausset J, Cann H, Cohen D, Lathrop M, Lalouel JM, White R. Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. Genomics. 1990 Mar;6(3):575–577. [PubMed] [Google Scholar]
  • Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J, Gilliam TC. A microsatellite genetic linkage map of human chromosome 18. Genomics. 1993 Jan;15(1):48–56. [PubMed] [Google Scholar]
  • Collins FS. Positional cloning moves from perditional to traditional. Nat Genet. 1995 Apr;9(4):347–350. [PubMed] [Google Scholar]
  • Olsen HS, Cepeda MA, Zhang QQ, Rosen CA, Vozzolo BL, Wagner GF. Human stanniocalcin: a possible hormonal regulator of mineral metabolism. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):1792–1796. [PMC free article] [PubMed] [Google Scholar]
  • Wagner GF, Vozzolo BL, Jaworski E, Haddad M, Kline RL, Olsen HS, Rosen CA, Davidson MB, Renfro JL. Human stanniocalcin inhibits renal phosphate excretion in the rat. J Bone Miner Res. 1997 Feb;12(2):165–171. [PubMed] [Google Scholar]
  • Azen EA, Maeda N. Molecular genetics of human salivary proteins and their polymorphisms. Adv Hum Genet. 1988;17:141–199. [PubMed] [Google Scholar]
  • Gibson MA, Hatzinikolas G, Kumaratilake JS, Sandberg LB, Nicholl JK, Sutherland GR, Cleary EG. Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25) J Biol Chem. 1996 Jan 12;271(2):1096–1103. [PubMed] [Google Scholar]
  • Oliva D, Calì L, Feo S, Giallongo A. Complete structure of the human gene encoding neuron-specific enolase. Genomics. 1991 May;10(1):157–165. [PubMed] [Google Scholar]
  • Levine MA, Smallwood PM, Moen PT, Jr, Helman LJ, Ahn TG. Molecular cloning of beta 3 subunit, a third form of the G protein beta-subunit polypeptide. Proc Natl Acad Sci U S A. 1990 Mar;87(6):2329–2333. [PMC free article] [PubMed] [Google Scholar]
  • Ansari-Lari MA, Muzny DM, Lu J, Lu F, Lilley CE, Spanos S, Malley T, Gibbs RA. A gene-rich cluster between the CD4 and triosephosphate isomerase genes at human chromosome 12p13. Genome Res. 1996 Apr;6(4):314–326. [PubMed] [Google Scholar]
  • Ansari-Lari MA, Shen Y, Muzny DM, Lee W, Gibbs RA. Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination. Genome Res. 1997 Mar;7(3):268–280. [PubMed] [Google Scholar]
  • Scriver CR, MacDonald W, Reade T, Glorieux RH, Nogrady B. Hypophosphatemic nonrachitic bone disease: an entity distinct from X-linked hypophosphatemia in the renal defect, bone involvement, and inheritance. Am J Med Genet. 1977;1(1):101–117. [PubMed] [Google Scholar]
  • Lyles KW, Burkes EJ, Ellis GJ, Lucas KJ, Dolan EA, Drezner MK. Genetic transmission of tumoral calcinosis: autosomal dominant with variable clinical expressivity. J Clin Endocrinol Metab. 1985 Jun;60(6):1093–1096. [PubMed] [Google Scholar]

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