Chromosome 10 humain 251717 27373150 2008-03-14T21:37:59Z Kuebi 193252 +[[de:Chromosom 10 (Mensch)]] [[Image:Chromosome 10.svg|right]] Le '''chromosome 10''' est un des 24 [[chromosome|chromosomes humains]]. C'est l'un des 22 [[autosome]]s. ==Caractéristiques du chromosome 10== * Nombre de [[Paire de base|paires de base]] : '''{{formatnum:135413628}}''' * Nombre de [[gène]]s : '''862''' * Nombre de [[gène|gènes connus]] : '''730''' * Nombre de [[gène|pseudo gènes]] : '''317''' * Nombre de variations des [[nucléotide]]s (S.N.P ou single nucleotide polymorphisme) : '''{{formatnum:473419}}''' ==Anomalies chromosomiques décrites au niveau du chromosome 10== ==Gènes localisés sur le chromosome 10== ==Maladies localisées sur le chromosome 10== * La nomenclature utilisée pour localiser un [[gène]] est décite dans l'article de celui-ci * Les maladies en rapport avec des anomalies génétiques localisées sur le chromosome 10 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 10 |---- 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; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome d'Apert]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101600 101600] | q26 | [[FGFR2 (Gène)|FGFR2]] | Fibroblast growth factor receptor 2 |---- | [[Syndrome de Pfeiffer]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101600 101600] | q26 | [[FGFR2 (Gène)|FGFR2]] | Fibroblast growth factor receptor 2 |---- | [[Syndrome de Crouzon]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123500 123500] | q26 | [[FGFR2 (Gène)|FGFR2]] | Fibroblast growth factor receptor 2 |---- | &nbsp; | &nbsp; | &nbsp; | q26 | &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; | q25 | &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; |---- | [[Hyperplasie congénitale des surrénales]]<br>Déficit en 17-alpha-hydroxylase | [[Transmission autosomique récessive|Récessive]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202110 202110] | q24.3 | [[CYP17A1 (Gène)|CYP17A1]] | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | q24 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Syndrome de Cowden]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176920 176920] | q23.31 | [[PTEN (gène)|PTEN]] | &nbsp; |---- | [[Syndrome de Bannayan-Riley-Ruvalcaba]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153480 153480] | q23.31; | [[PTEN (gène)|PTEN]] | &nbsp; |---- | [[Syndrome de Protée]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176920 176920] | q23.31 | [[PTEN (gène)|PTEN]] | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | q23 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Lymphohistiocytose familiale]] | [[Transmission autosomique récessive|Récessive]] | &nbsp; | q22 | <small>Gène inconnu</small> | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | q22 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | [[Maladie de Charcot-Marie-Tooth type 4|Maladie de Charcot-Marie-Tooth type 4E]] | [[Transmission autosomique récessive|Récessive]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129010 129010] | q21.1-q22.1 | [[EGR2 (Gène)|EGR2]] | Early growth response protein 2 |---- | [[Maladie de Charcot-Marie-Tooth type 1|Maladie de Charcot-Marie-Tooth type 1D]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=607678 607678] | q21.1-q22.1 | [[EGR2 (Gène)|EGR2]] | Early growth response protein 2 |---- | &nbsp; | &nbsp; | &nbsp; | q21 | &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; |---- | [[Maladie de Hirschsprung|Maladie de Hirschsprung non syndromique]] | [[Transmission autosomique dominante|Dominante]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142623 142623] | q11.2 | [[RET (Gène)|RET]] | Proto-oncogene tyrosine-protein kinase receptor |---- | &nbsp; | &nbsp; | &nbsp; | q11 | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- ! colspan="6" style="background-color:#d3d3d3" | Bras court |---- | &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; | p11 | &nbsp; | &nbsp; |---- | [[Maladie de Refsum]] | [[Transmission autosomique récessive|Récessive]] | [http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266500 266500] | 10pter-p11.2 | [[PHYH (Gène)|PHYH]] | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &nbsp; |---- | &nbsp; | &nbsp; | &nbsp; | &nbsp; | &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; | p13 | &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; | p14 | &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; | p15 | &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; |} ==Les autres chromosomes== {{Chromosome humain}} ==Sources== * {{en}} '''Ensembl 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]] [[de:Chromosom 10 (Mensch)]] [[en:Chromosome 10 (human)]] [[es:Cromosoma 10 (humano)]] [[hu:Humán 10-es kromoszóma]] [[it:Cromosoma 10 (umano)]] [[no:Kromosom 10]] [[pl:Chromosom 10]] [[pt:Cromossoma 10 (humano)]] [[sr:Хромозом 10 (човек)]] [[tr:Kromozom 10]]