Literature DB >> 3422213

A regional localisation for an X-linked suppressor gene (XS) for the Lutheran blood group.

J C Mulley1, P C Norman, P Tippett, R W Beal.   

Abstract

Suppression of Lutheran blood group expression is usually associated with an autosomal dominant suppressor gene In(Lu) which results in the rare Lu(a--b--) phenotype. X-linked recessive suppression can also occur under the control of the XS locus with normal (XS1) and suppressor (XS2) alleles. The only known kindred with XS2 segregating was examined for polymorphic DNA markers with known regional localisations on the X chromosome. Two point linkage analysis suggested linkage of XS to DXS14 (p58.1) with theta = 0.00, z = 1.96. DXS14 is situated near the centromere at Xp11. Recombinants with DXS84 (distal to DXS14 on Xp) and recombinants with DXYS1 (pDP34) (on the proximal part of Xq) suggests a localisation for XS near the centromere, between DXS84 and DXYS1 (Xp21.2-Xq21.1). Linkage to a marker on the X chromosome confirms the original assignment of XS to the X chromosome, which was based on pedigree inspection from this family.

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Year:  1988        PMID: 3422213     DOI: 10.1007/BF00278180

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  12 in total

1.  X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Authors:  U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.

Authors:  D F Callen; J C Mulley; E G Baker; G R Sutherland
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

3.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

4.  Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.

Authors:  P N Goodfellow; K E Davies; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1985

5.  Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques.

Authors:  H F Willard; M H Skolnick; P L Pearson; J L Mandel
Journal:  Cytogenet Cell Genet       Date:  1985

6.  The recessive Lu(a-b-) phenotype. A family study.

Authors:  F Brown; S Simpson; S Cornwall; B P Moore; R Oyen; W L Marsh
Journal:  Vox Sang       Date:  1974-03       Impact factor: 2.144

7.  The genetics of a dominant inhibitor of the Lutheran antigens.

Authors:  V Taliano; R M Guévin; P Tippett
Journal:  Vox Sang       Date:  1973-01       Impact factor: 2.144

8.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

9.  Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.

Authors:  J C Mulley; A K Gedeon; K A Thorn; L J Bates; G R Sutherland
Journal:  Am J Med Genet       Date:  1987-06

10.  Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis.

Authors:  A de la Chapelle; E M Sankila; M Lindlöf; P Aula; R Norio
Journal:  Clin Genet       Date:  1985-10       Impact factor: 4.438

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  1 in total

1.  Molecular Bases and Genotyping for Rare Blood Types.

Authors:  Christof Jungbauer
Journal:  Transfus Med Hemother       Date:  2009-05-26       Impact factor: 3.747

  1 in total

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