| References |
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Bernardi G
(2000)
Isochores and the evolutionary genomics of vertebrates.
Gene
241: 3–17.
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Dehal P,
Predki P,
Olsen AS, et al.
(2001)
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution.
Science
293: 104–111.
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book
Hammarström S,
Olsen A,
Teglund S and
Baranov V
(1998)
"The nature and expression of the human CEA family".
In: Stanners C (ed.)
Cell Adhesion and Communication Mediated by the CEA Family. Basic and Clinical Perspectives,
pp. 1–30.
Amsterdam: Harwood Academic Publishers.
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Hoffman SMG,
Nelson DR and
Keeney DS
(2001)
Organization, structure and evolution of the CYP2 gene cluster on human chromosome 19.
Pharmacogenetics
11: 687–698.
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International Human Genome Sequencing Consortium
(2001)
Initial sequencing and analysis of the human genome.
Nature
409: 860–921.
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Kim J,
Bergmann A and
Stubbs L
(2000)
Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3).
Genomics
64: 114–118.
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Kim J,
Bergmann A,
Wehri E,
Lu X and
Stubbs L
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Imprinting and evolution of two kruppel-type zinc-finger genes, ZIM3 and ZNF264, located in the PEG3/USP29 imprinted domain.
Genomics
77: 91–98.
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Kim J,
Gordon L,
Dehal P, et al.
(2001b)
Homology-driven assembly of a sequence-ready mouse BAC contig map spanning regions related to the 46mb gene-rich euchromatic segments of human chromosome 19.
Genomics
74: 129–141.
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Mohrenweiser HW,
Tsujimoto S,
Gordon L and
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Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19.
Genomics
47: 153–162
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Morton NE
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88: 7474–7476.
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| Further Reading |
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other
Further information about chromosome 19 can be found by following the Web Links below.
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| Web Links |
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ePath
Cancer Genome Anatomy Project. Mitelman database of chromosome aberrations in cancer. Information on chromosome aberrations in cancer and their relation to tumor characteristics.
http://cgap.nci.nih.gov/Chromosomes/Mitelman
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ePath
CEPH Genotype Database. Genotypes for all genetic markers that have been typed in the CEPH reference families for linkage mapping of human chromosomes
http://www.cephb.fr/cephdb/
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ePath
Cooperative Human Linkage Center. Information on microsatellite genetic markers and mapsdeveloped by the Cooperative Human Linkage Center
http://gai.nci.nih.gov/CHLC/
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ePath
DOE Joint Genome Institute. Information on sequencing of human chromosome 19 and homologous regions of the mouse genome
http://www.jgi.doe.gov/
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ePath
Ensembl Genome Browser. Viewer display of automated annotation of human genome sequence
http://www.ensembl.org/
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ePath
GDB Human Genome Database. Updated daily. Descriptions of regions of the human genome, including genes, markers, clones and contigs, maps of the human genome and variations within the genome
http://www.gdb.org/
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ePath
Genew: Human Gene Nomenclature Database Search Engine. Approved names and symbols for human genes, together with aliases and previous symbols
http://www.gene.ucl.ac.uk/cgi-bin/nomenclature/searchgenes.pl
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ePath
Human Genome Organization (HUGO) Chromosome 19 home page. Provides links to a variety of chromosome 19 resource sites
http://www.gdb.org/hugo/chr19/
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ePath
Jackson Laboratory Mouse Genome Informatics. Information on mouse genes, genetic markers, phenotypes, and comparative mapping data
http://www.informatics.jax.org/
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ePath
Lawrence Livermore National Laboratory. Maps of human chromosome 19. Access to restriction maps, FISH maps and metric physical map of chromosome 19
http://bbrp.llnl.gov/bbrp/genome/html/chrom_map.html
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ePath
Marshfield Clinic. Center for Medical Genetics. Comprehensive human genetic linkage maps and comparison of genetic and physical maps for human chromosomes
http://research.marshfieldclinic.org/genetics/
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ePath
National Center for Biotechnology Information: Online Mendelian Inheritance in Man (OMIM). Catalog of human genes and genetic disorders
http://www.ncbi.nlm.nih.gov/Omim/
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ePath
NCBI Human Genome. Status of human genome sequencing and guide to online resources and tools for analysis of genome sequence
http://www.ncbi.nlm.nih.gov/genome/seq/
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ePath
NCBI LocusLink. Information about genetic loci, including official nomenclature, sequence accessions, phenotypes, homology, and map locations
http://www.ncbi.nlm.nih.gov/LocusLink/
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ePath
NCBI Single Nucleotide Polymorphism dbSNP. Database of single nucleotide polymorphisms identified in human DNA sequence
http://www.ncbi.nlm.nih.gov/SNP/
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ePath
SNP Consortium Ltd. Information on single nucleotide polymorphisms discovered and characterized by the SNP Consortium
http://snp.cshl.org/
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ePath
Stanford Human Genome Center. Finishing status of chromosome 19 genomic clones, with access to sequence currently in the finishing process
http://www-shgc.stanford.edu/index.html
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ePath
Weizmann Institute of Science, Bioinformatics Unit and Genome Center. GeneCards. Database of human genes, gene products and their involvement in diseases
http://bioinformatics.weizmann.ac.il/cards/
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