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20-September-2008 09:55:52 - 9 human Redirected from Chromosome 9 Chromosome 9 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 9 spans about 145 million base pairs of nucleic acids the building blocks of DNA and represents between 4 and 4.5 percent of the total DNA in cells. Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 9 likely contains between 800 and 1,200 genes. Genes The following are some of the genes located on chromosome 9: ABO: ABO histo-blood group glycosyltransferases ADAMTS13: ADAM metallopeptidase with thrombospondin type 1 motif, 13 ALAD: aminolevulinate, delta-, dehydratase ALS4: amyotrophic lateral sclerosis 4 ASS: argininosuccinate synthetase CCL21: chemokine C-C motif ligand 21, SCYA21 CCL27: chemokine C-C motif ligand 27, SCYA27 COL5A1: collagen, type V, alpha 1 ENG: endoglin Osler-Rendu-Weber syndrome 1 FXN: frataxin GALT: galactose-1-phosphate uridylyltransferase GRHPR: glyoxylate redasductase/hydroxypyruvate reductase IKBKAP: inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein TMC1: transmembrane channel-like 1 TSC1: tuberous sclerosis 1 Diseases disorders The following diseases are some of those related to genes on chromosome 9: ALAD deficiency porphyria amyotrophic lateral sclerosis ALS citrullinemia Ehlers-Danlos syndrome Ehlers-Danlos syndrome, classical type familial dysautonomia Friedreich ataxia galactosemia Gorlin syndrome or Nevoid Basal Cell Carcinoma syndrome herary hemorrhagic telangiectasia Nail-patella syndrome NPS nonsyndromic deafness nonsyndromic deafness, autosomal dominant nonsyndromic deafness, autosomal recessive porphyria primary hyperoxaluria thrombotic thrombocytopenic purpura tuberous sclerosis References Gilbert F, Kauff N 2001. Disease genes and chromosomes: disease maps of the human genome. Chromosome 9. Genet Test 5 2: 157-74. doi:10.1089/109065701753145664. PMID 11551106. Humphray SJ, Oliver K, Hunt AR, et al. 2004. DNA sequence and analysis of human chromosome 9. Nature 429 6990: 369-74. doi:10.1038/nature02465. PMID 15164053. Wicking C, Berkman J, Wainwright B 1994. Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome. Chromosome 9. Genomics 22 3: 505-11. doi:10.1006/geno.1994.1423. PMID 8001963. This genetics article is a stub. v d e Human chromosomes 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · 11 · 12 · 13 · 14 · 15 · 16 · 17 · 18 · 19 · 20 · 21 · 22 · X · Y Retrieved from http://en..org/wiki/Chromosome_9_human Categories: Genetics stubs | Chromosomes Views Article Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page Languages Deutsch Français Italiano Magyar Nederlands ‪Norsk bokmÃ¥l‬ Polski Português СрпÑ?ки / Srpski Türkçe 䏿–‡ This page was last modified on 10 August 2008, at 23:49
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