Literature DB >> 1478646

Closure of a genetic linkage map of human chromosome 7q with centromere and telomere polymorphisms.

C Helms1, S K Mishra, H Riethman, A K Burgess, S Ramachandra, C Tierney, D Dorsey, H Donis-Keller.   

Abstract

We have constructed a 2.4-cM resolution genetic linkage map for chromosome 7q that is bounded by centromere and telomere polymorphisms and contains 66 loci (88 polymorphic systems), 38 of which are uniquely placed with odds for order of at least 1000:1. Ten genes are included in the map and 11 markers have heterozygosities of at least 70%. This map is the first to incorporate several highly informative markers derived from a telomere YAC clone HTY146 (locus D7S427), including HTY146c3 (HET 92%). The telomere locus markers span at least 200 kb of the 7q terminus and no crossovers within the physical confines of the locus were observed in approximately 240 jointly informative meioses. The sex-equal map length is 158 cM and the largest genetic interval between uniquely localized markers in this map is 11 cM. The female and male map lengths are 181 and 133 cM, respectively. The map is based on the CEPH reference pedigrees and includes over 4000 new genotypes, our previously reported data plus 29 allele systems from the published CEPH version 5 database, and was constructed using the program package CRI-MAP. This genetic linkage map can be considered a baseline map for 7q, and will be useful for defining the extent of chromosome deletions previously reported for breast and prostate cancers, for developing additional genetic maps such as index marker and 1-cM maps, and ultimately for developing a fully integrated genetic and physical map for this chromosome.

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Year:  1992        PMID: 1478646     DOI: 10.1016/s0888-7543(05)80128-4

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  5 in total

1.  VNTR and microsatellite polymorphisms within the subtelomeric region of 7q.

Authors:  A V Hing; C Helms; H Donis-Keller
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

2.  High-resolution skim genotyping by sequencing reveals the distribution of crossovers and gene conversions in Cicer arietinum and Brassica napus.

Authors:  Philipp E Bayer; Pradeep Ruperao; Annaliese S Mason; Jiri Stiller; Chon-Kit Kenneth Chan; Satomi Hayashi; Yan Long; Jinling Meng; Tim Sutton; Paul Visendi; Rajeev K Varshney; Jacqueline Batley; David Edwards
Journal:  Theor Appl Genet       Date:  2015-03-10       Impact factor: 5.699

3.  Frequent recombination in the human T-cell receptor beta gene complex.

Authors:  C E Day; K Schmitt; M A Robinson
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

Review 4.  Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.

Authors:  A O Wilkie
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

Review 5.  Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

Authors:  S W Scherer; P Poorkaj; T Allen; J Kim; D Geshuri; M Nunes; S Soder; K Stephens; R A Pagon; M A Patton
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

  5 in total

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