Literature DB >> 9585587

Haplotype mapping of a major quantitative-trait locus for fetal hemoglobin production, on chromosome 6q23.

C Garner1, J Mitchell, T Hatzis, J Reittie, M Farrall, S L Thein.   

Abstract

Fetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and are influenced by several genetic variants; the major determinants appear to be unlinked to the beta-globin gene cluster. Recently, a trans-acting locus controlling Hb F and FC production has been mapped to chromosome 6q23 in an Asian Indian kindred that includes individuals with heterocellular hereditary persistence of Hb F (HPFH) associated with beta thalassemia. We have extended the kindred by 57 members, bringing the total studied to 210, and have saturated the region with 26 additional markers. Linkage analysis showed tight linkage of the quantitative-trait locus (QTL) to the anonymous markers D6S976 (LOD score 11.3; recombination fraction .00) and D6S270 (LOD score 7.4; recombination fraction .00). Key recombination events now place this QTL within a 1-2-cM interval spanning approximately 1.5 Mb between D6S270 and D6S1626. Furthermore, haplotype analysis has led to a reevaluation of the genealogy and to the identification of additional relationships in the kindred.

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Year:  1998        PMID: 9585587      PMCID: PMC1377138          DOI: 10.1086/301859

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  22 in total

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Review 4.  Hemoglobin switching and its clinical implications.

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Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

7.  Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.

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  22 in total

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Review 4.  Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.

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Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-30       Impact factor: 11.205

7.  A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia.

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8.  Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.

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9.  Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.

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10.  Transgenic knockout mice exclusively expressing human hemoglobin S after transfer of a 240-kb betas-globin yeast artificial chromosome: A mouse model of sickle cell anemia.

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Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-08       Impact factor: 11.205

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