Chromosome 7 humain 251714 30628294 2008-06-14T10:17:00Z Padawane 19117 /* Sources */ cat [[Image:Chromosome 7.svg|right|200x400px]] Le '''chromosome 7''' est un des 24 [[chromosome|chromosomes humains]]. C'est l'un des 22 [[autosome]]s. ==Caractéristiques du chromosome 7== * Nombre de [[Paire de base|paires de base]] : '''{{formatnum:158628139}}''' * Nombre de [[gène]]s : '''{{formatnum:1116}}''' * Nombre de [[gène|gènes connus]] : '''916''' * Nombre de [[gène|pseudo gènes]] : '''454''' * Nombre de variations des [[nucléotide]]s (S.N.P ou single nucleotide polymorphisme) : '''{{formatnum:489908}}''' ==Anomalies chromosomiques décrites au niveau du chromosome 7== * [[Syndrome de Silver-Russel]] * [[Mucoviscidose]] ([[gène CFTR]]) ==Gènes localisés sur le chromosome 7== [[PIP (gène)|PIP]], localisé en 7q32-36 ==Maladies localisées sur le chromosome 7== * La nomenclature utilisée pour localiser un [[gène]] est décrite dans l'article de celui-ci * Les maladies en rapport avec des anomalies génétiques localisées sur le chromosome 7 sont : <br /> {| width="100%" border="1" cellpadding="4" cellspacing="0" style="page-break-before: always; page-break-inside: avoid" ! colspan="6" style="background-color:#b3b3b3" | Maladies localisées sur le chromosome 7 |---- style="background-color:#b3b3b3" | width="37%" | Pathologie | width="10%" | Transmission | width="9%" | O.M.I.M | width="4%" | Locus | width="10%" | Gène | width="30%" | Protéine codée par le gène |---- ! colspan="6" style="background-color:#d3d3d3" | Bras long |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Holoproencéphalie]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q36 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome de Romano-Ward]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q35 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q33 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q32 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Mucoviscidose]] | &nbsp; | &nbsp; | Q31.2 | &nbsp; | &nbsp;C.F.T.R. (cystic fibrosys transmembrane conductance régulator) |---- | [[Maladie du sirop d'érable]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome de Pendred]] | &nbsp; | &nbsp; | Q31 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Microlissencéphalie]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q22 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Dystonie myoclonique]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Hyperthermie maligne]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q21 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome de Williams]] | &nbsp; | &nbsp; | Q11.23 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q11 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | Q11 | &nbsp; | &nbsp; |---- | [[Dystrophie musculaire des ceintures|Dystrophie musculaire des ceintures Type 1D]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Maladie de Charcot-Marie-Tooth type 2]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- ! colspan="6" style="background-color:#d3d3d3" | Bras court |---- | &nbsp; | &nbsp; | &nbsp; | P11 | &nbsp; | &nbsp; |---- | [[Syndrome de Silver-Russel]] | &nbsp; | &nbsp; | P11.2 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | P12 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | P13 | &nbsp; | &nbsp; |---- | [[Syndrome de Greig]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome de Pallister-Hall]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | P14 | &nbsp; | &nbsp; |---- | [[Syndrome main pied utérus]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=140000 140000] | p14.2-p15 | [[HOXA13(Gène)|HOXA13]] | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | p15 | &nbsp; | &nbsp; |---- | [[Maladie de Charcot-Marie-Tooth type 2]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Surdité d'origine génétique]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | P21 | &nbsp; | &nbsp; |---- | [[Syndrome de Saethre-Chotzen]] | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | P22 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |} ==Les autres chromosomes== {{Chromosome humain}} ==Sources== * {{en}} '''Ensemble Genome Browser''' [http://www.ensembl.org/] * {{en}} Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD.[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM] {{portail médecine}} [[Catégorie:chromosome humain|Chromosome 07 humain]] [[de:Chromosom 7 (Mensch)]] [[en:Chromosome 7 (human)]] [[hu:Humán 7-es kromoszóma]] [[it:Cromosoma 7 (umano)]] [[no:Kromosom 7]] [[pl:Chromosom 7]] [[pt:Cromossoma 7 (humano)]] [[sr:Хромозом 7 (човек)]] [[tr:Kromozom 7]] [[zh:7號染色體 (人類)]]