http://www.ncbi.nlm.nih.gov/genome/guide/HsChr2.shtml
Human Chr 2 Pubmed Entrez BLAST OMIM Taxonomy Structure Search Contigs dbsts Genbank Genemap '99 Locuslink MEDLINE OMIM Unigene for Human Genome Resources Select a Chromosome: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y Mapviewer Chr 2 Locuslink Chr. 2 Loci Unigene Chr. 2 Clusters Mouse Homologies for Human Chr. 2 Chromosome 2 Disease Genes Some diseases associated with chromosome 2 mutations Alstrom Syndrome Holoprosencephaly 2 Tibial Muscular_dystrophy Autosomal Recessive Deafness -9 Limb Girdle Muscular_dystrophy 2b See OMIM or Genes and Disease for additional examples and detailed information. OMIM Home_page OMIM Morbid Map Genes and Disease Sequencing Progress Euchromatic size: 255000 kb Finished sequence: 221704 kb Percent finished: 86.9%Number of contigs: 183 List contigs by size List contigs by position Sequencing is being coordinated by The Sanger Center. Major contributions have come from: The Sanger Center Washington University The Whitehead Institute STS Maps Map STSS Type Ref Genemap'99 2257 RH 1 Whitehead 1275 YAC 2 Stanford 934 RH 3 Genethon 233 Link 4 Cytogenetics Mitelman et_al. 5) have_cataloged recurrent chromosome aberrations associated with cancers. Chromosome 2 aberrations References 1 Deloukas et_al. 1998). ) A physical map of 30,000 human genes. Science 282,744-746.2 Hudson et_al. 1995). ) An STS-based map of the human genome. Science 270,1945-1954.3 Stewart et_al. 1997). ) An STS-based radiation hybrid map of the human genome. Genome Res 7, 422-433.4 Dib, et_al. 1995). ) A comprehensive genetic map of the human genome based_on 5, 264 microsatellites. Nature 380,152-154.5 Mitelman, et_al. 1997). ) A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet Apr 15 Suppl. 417-474. Comments or Questions? Write to the NCBI Service Desk