http://www.ncbi.nlm.nih.gov/genome/guide/HsChr9.shtml
Human Chr 9 Pubmed Entrez BLAST OMIM Taxonomy Structure Search Genbank Genemap'99 Locuslink MEDLINE OMIM Unigene Maps dbsts 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 9 Locuslink Chr. 9 Loci Unigene Chr. 9 Clusters Mouse Homologies for Human Chr. 9 Chromosome 9 Disease Genes Friedreich's Ataxia is a rare disorder involving progressive loss of voluntary muscular coordination. Some diseases associated with chromosome 9 mutations Dysautonomia Friedreich_ataxia Torsion Dystonia 1 Fanconi_anemia, Type C Nail-patella_syndrome 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: 145000 kb Finished sequence: 108667 kb Percent finished: 74.9%Number of contigs: 88 List contigs by size List contigs by position Sequencing is being coordinated by the Sanger Center. Major contributions have come from: The Whitehead Institute STS Maps Map STSS Type Ref Genemap'99 1248 RH 1 Whitehead 577 YAC 2 Stanford 419 RH 3 Genethon 189 Link 4 Cytogenetics Mitelman et_al. 5) have_cataloged recurrent chromosome aberrations associated with cancers. Chromosome 9 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