Literature DB >> 8666401

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.

D F Callen1, S A Lane, H Kozman, G Kremmidiotis, S A Whitmore, M Lowenstein, N A Doggett, N Kenmochi, D C Page, D R Maglott.   

Abstract

A single mapping resource, a mouse/human somatic cell panel with average distance between breakpoints of 1.2 Mb and a potential resolution of 1 Mb, has been utilized to integrate the genetic map and a transcript map of human chromosome 16. This map includes 141 genetic markers and 200 genes and transcripts. The localization of four genes (CHEL3, TK2, TRG1, and MMP9) reported to map to chromosome 16 could not be confirmed, and for three of these localizations to other human chromosomes are reported. A correlation between genetic and physical distance over a region estimated to be 23 Mb on the short arm of chromosome 16 identified an interval demonstrating a greatly increased rate of recombination where, in females, 1 cM is equivalent to a physical distance of 100 kb.

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Year:  1995        PMID: 8666401     DOI: 10.1006/geno.1995.9005

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


  7 in total

1.  High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.

Authors:  J Becker-Follmann; A Gaa; E Baùsch; E Natt; G Scherer; O von Deimling
Journal:  Mamm Genome       Date:  1997-03       Impact factor: 2.957

2.  Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.

Authors:  P Szepetowski; J Rochette; P Berquin; C Piussan; G M Lathrop; A P Monaco
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

3.  Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.

Authors:  A Iida; R Isobe; M Yoshimoto; F Kasumi; Y Nakamura; M Emi
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

4.  A comprehensive, high-resolution genomic transcript map of human skeletal muscle.

Authors:  S Bortoluzzi; L Rampoldi; B Simionati; R Zimbello; A Barbon; F d'Alessi; N Tiso; A Pallavicini; S Toppo; N Cannata; G Valle; G Lanfranchi; G A Danieli
Journal:  Genome Res       Date:  1998-08       Impact factor: 9.043

5.  The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.

Authors:  Kavita Bhalla; Hilary A Phillips; Joanna Crawford; Olivia L D McKenzie; John C Mulley; Helen Eyre; Alison E Gardner; Gabriel Kremmidiotis; David F Callen
Journal:  J Hum Genet       Date:  2004-05-18       Impact factor: 3.172

6.  Analysis of PKD1 for genomic deletion by multiplex ligation-dependent probe assay: absence of hot spots.

Authors:  Piotr Kozlowski; John Bissler; York Pei; David J Kwiatkowski
Journal:  Genomics       Date:  2007-12-03       Impact factor: 5.736

7.  Transgene integration - an analysis in autotransgenic Labeo rohita Hamilton (Pisces: Cyprinidae).

Authors:  R Rajesh; K C Majumdar
Journal:  Fish Physiol Biochem       Date:  2005-04       Impact factor: 2.794

  7 in total

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