Chromosome 11 (human): Difference between revisions

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__NOTOC__
{{Infobox chromosome
{{CMG}} {{AE}} {{JC}}
| image = Human male karyotpe high resolution - Chromosome 11 cropped.png
[[image:Chromosome_11.svg|125px|right]]
| caption = Human chromosome 11 pair after [[G banding|G-banding]].<br/>One is from mother, one is from father.
| image2 = Human male karyotpe high resolution - Chromosome 11.png
| caption2 = Chromosome 11 pair<br/> in human male [[karyogram]].
| length_bp = 135,086,622 bp<br/>([[GRCh38]])<ref name="National Center for Biotechnology Information 2017">{{cite web | title=Human Genome Assembly GRCh38 - Genome Reference Consortium | website=National Center for Biotechnology Information | date=2013-12-24 | url=https://www.ncbi.nlm.nih.gov/grc/human/data?asm=GRCh38 | language=en | accessdate=2017-03-04}}</ref>
| genes = 1,224 ([[Consensus CDS Project|CCDS]])
| type = [[Autosome]]
| centromere_position = [[Centromere#Submetacentric|Submetacentric]]<ref name="StrachanRead2010">{{cite book|author1=Tom Strachan|author2=Andrew Read|title=Human Molecular Genetics|url=https://books.google.com/books?id=dSwWBAAAQBAJ&pg=PA45|date=2 April 2010|publisher=Garland Science|isbn=978-1-136-84407-2|page=45}}</ref><br/>(53.4 Mbp<ref name="850bphs">Genome Decoration Page, NCBI.  [ftp://ftp.ncbi.nlm.nih.gov/pub/gdp/ideogram_9606_GCF_000001305.14_850_V1 Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3)]. Last update 2014-06-03. Retrieved 2017-04-26.</ref>)
| ensembl_id = 11
| entrez_id = 11
| ncbi_id = 11
| ucsc_id = 11
| refseq_id = NC_000011
| genbank_id = CM000673
}}
'''Chromosome 11''' is one of the 23 pairs of [[chromosome]]s in [[human]]s. Humans normally have two copies of this chromosome. Chromosome 11 spans about 135 million [[base pair]]s (the building material of [[DNA]]) and represents between 4 and 4.5 percent of the total DNA in [[cell (biology)|cells]].


==Overview==
At 21.5 genes per [[Base pair#Length measurements|megabase]], Chromosome 11 is one of the most gene-rich, and disease-rich, chromosomes in the [[human genome]].
'''Chromosome 11''' is one of the 23 pairs of [[chromosome]]s in [[human]]s. People normally have two copies of this chromosome. Chromosome 11 spans about 134.5 million [[base pair]]s (the building material of [[DNA]]) and represents between 4 and 4.5 percent of the total DNA in [[cell (biology)|cells]]. It is one of the most gene- and disease-rich chromosomes in the [[human genome]].


Identifying [[gene]]s 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 11 likely contains between 1,300 and 1,700 genes.
More than 40% of the 856 [[olfactory receptor]] genes in the human genome are located in 28 single-gene, and multi-gene, clusters along this chromosome.


A recent study <ref>{{cite journal | author=Taylor TD, Noguchi H, Totoki Y, Toyoda A, Kuroki Y, Dewar K, Lloyd C, Itoh T, Takeda T, Kim DW, She X, Barlow KF, Bloom T, Bruford E, Chang JL, Cuomo CA, Eichler E, FitzGerald MG, Jaffe DB, LaButti K, Nicol R, Park HS, Seaman C, Sougnez C, Yang X, Zimmer AR, Zody MC, Birren BW, Nusbaum C, Fujiyama A, Hattori M, Rogers J, Lander ES, Sakaki Y | title=Human chromosome 11 DNA sequence and analysis including novel gene identification | journal=Nature | year=2006 | pages=497-500 | volume=440 | issue=7083  | id=PMID 16554811}}</ref> shows that 11.6 genes per megabase, including 1,524 protein-coding genes and 765 [[pseudogene]]s can be found on chromosome 11.
==Genes==
{{Category see also|Genes on human chromosome 11}}
The following are some of the gene count estimates of human chromosome 11. Because researchers use different approaches to [[genome annotation]] their predictions of the [[number of genes]] on each chromosome varies (for technical details, see [[gene prediction]]). Among various projects, the collaborative consensus coding sequence project ([[Consensus CDS Project|CCDS]]) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.<ref name="pmid20441615">{{cite journal| author=Pertea M, Salzberg SL| title=Between a chicken and a grape: estimating the number of human genes. | journal=Genome Biol | year= 2010 | volume= 11 | issue= 5 | pages= 206 | pmid=20441615 | doi=10.1186/gb-2010-11-5-206 | pmc=2898077 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20441615  }} </ref>


More than 40% of the 856 [[olfactory receptor]] genes in the human genome are located in 28 single- and multi-gene clusters along this chromosome.  
{| class="wikitable" style="text-align:right"
| Estimated by || [[Protein-coding genes]] || [[Non-coding RNA|Non-coding RNA gene]]s || [[Pseudogene]]s || Source || Release date
|-
| [[Consensus CDS Project|CCDS]] || 1,224 || - || -
|style="text-align:center"| <ref name="CCDS">{{cite web | title=Search results - 11&#91;CHR&#93; AND "Homo sapiens"&#91;Organism&#93; AND ("has ccds"&#91;Properties&#93; AND alive&#91;prop&#93;)  - Gene | website= NCBI |version = CCDS Release 20 for ''Homo sapiens'' | url=https://www.ncbi.nlm.nih.gov/gene?term=11%5BChr%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22has%20ccds%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch |date=2016-09-08 | accessdate=2017-05-28}}</ref>
| 2016-09-08
|-
| [[HUGO Gene Nomenclature Committee|HGNC]]|| 1,262 || 271 || 666
|style="text-align:center"| <ref name="HGNC20170512">{{cite web | title=Statistics & Downloads for chromosome 11 | website=HUGO Gene Nomenclature Committee | url=http://www.genenames.org/cgi-bin/statistics?c=11  |date=2017-05-12 | accessdate=2017-05-19}}</ref>
| 2017-05-12
|-
| [[Ensembl genome database project|Ensembl]] || 1,301 || 1,060 || 811
|style="text-align:center"| <ref name="Ensembl Release 88">{{cite web | title=Chromosome 11: Chromosome summary - Homo sapiens | website= Ensembl Release 88 | url=http://mar2017.archive.ensembl.org/Homo_sapiens/Location/Chromosome?r=11 |date=2017-03-29 | accessdate=2017-05-19}}</ref>
| 2017-03-29
|-
| [[National Center for Biotechnology Information|NCBI]] || 1,314 || 860 || 839
|style="text-align:center"| <ref name="NCBI coding">{{cite web | title=Search results - 11&#91;CHR&#93; AND "Homo sapiens"&#91;Organism&#93; AND ("genetype protein coding"&#91;Properties&#93; AND alive&#91;prop&#93;)  - Gene | website=NCBI | date=2017-05-19 | url=https://www.ncbi.nlm.nih.gov/gene?term=11%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20protein%20coding%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch | accessdate=2017-05-20}}</ref><ref name="NCBI noncoding">{{cite web | title=Search results - 11&#91;CHR&#93; AND "Homo sapiens"&#91;Organism&#93; AND ( ("genetype miscrna"&#91;Properties&#93; OR "genetype ncrna"&#91;Properties&#93; OR "genetype rrna"&#91;Properties&#93; OR "genetype trna"&#91;Properties&#93; OR "genetype scrna"&#91;Properties&#93; OR "genetype snrna"&#91;Properties&#93; OR "genetype snorna"&#91;Properties&#93;) NOT "genetype protein coding"&#91;Properties&#93; AND alive&#91;prop&#93;) - Gene | website=NCBI | date=2017-05-19 | url=https://www.ncbi.nlm.nih.gov/gene?term=11%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%28%22genetype%20miscrna%22%5BProperties%5D%20OR%20%22genetype%20ncrna%22%5BProperties%5D%20OR%20%22genetype%20rrna%22%5BProperties%5D%20OR%20%22genetype%20trna%22%5BProperties%5D%20OR%20%22genetype%20scrna%22%5BProperties%5D%20OR%20%22genetype%20snrna%22%5BProperties%5D%20OR%20%22genetype%20snorna%22%5BProperties%5D%29%20NOT%20%22genetype%20protein%20coding%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch | accessdate=2017-05-20}}</ref><ref name="NCBI pseudo">{{cite web | title=Search results - 11&#91;CHR&#93; AND "Homo sapiens"&#91;Organism&#93; AND ("genetype pseudo"&#91;Properties&#93; AND alive&#91;prop&#93;)  - Gene | website=NCBI | date=2017-05-19 | url=https://www.ncbi.nlm.nih.gov/gene?term=11%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20pseudo%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch | accessdate=2017-05-20}}</ref>
| 2017-05-19
|}


==Genes==
The following are some of the genes located on chromosome 11:
The following are some of the genes located on chromosome 11:
* [[ACAT1]]: acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)
* [[ACAT1]]: acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)
* [[ACRV1]]: encoding [[protein]] Acrosomal protein SP-10
* [[AKIP1]]: A kinase interacting protein 1
* [[Alkb homolog 3, alpha-ketoglutaratedependent dioxygenase|ALKBH3]] encoding [[protein]] AlkB homolog 3, alpha-ketoglutaratedependent dioxygenase
* [[Angiomotin-like protein 1|AMOTL1]]: angiomotin-like protein 1
* [[AMPD3]]: encoding [[enzyme]] AMP deaminase 3
* [[API5]]: encoding [[protein]] Apoptosis inhibitor 5
* [[Apelin receptor|APLNR]]:  Apelin receptor (APJ receptor)
* [[APOA4]]: apolipoprotein A-IV
* [[Archain 1|ARCN1]] encoding [[protein]] Archain 1
* [[ASRGL1]]: encoding [[enzyme]] L-asparaginase
* [[Ataxia telangiectasia mutated|ATM]]: ataxia telangiectasia mutated (includes complementation groups A, C and D)
* [[Ataxia telangiectasia mutated|ATM]]: ataxia telangiectasia mutated (includes complementation groups A, C and D)
* [[B3GNT1]]: encoding [[enzyme]] [[N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase]]
* [[BDNF]]: secretes BDNF,  a member of the Neurotrophin family of proteins
* [[C11orf1]]: encoding [[protein]]
* [[C11orf16]]: encoding [[protein]] Uncharacterized protein C11orf16
* [[C11orf49]]: encoding [[protein]] UPF0705 protein C11orf49
* [[C11orf52]] encoding [[protein]] C11orf52
* [[C11orf54]]: encoding [[protein]] Ester hydrolase C11orf54
* [[C11orf58]]: small acidic protein
* [[C11orf73]]: chromosome 11, open reading frame 73
* [[C11orf86]]: encoding [[protein]] Uncharacterized protein C11orf86
* [[C1QTNF4 (gene)|C1QTNF4]] encoding [[protein]] C1q and tumor necrosis factor related protein 4
* [[C1QTNF5]]: encoding [[protein]] C1q and tumor necrosis factor related protein 5
* [[Caprin-1|CAPRIN1]]: encoding protein, cell cycle associated protein 1
* [[CCDC90B]]: coiled coil domain containing 90B
* [[CCL9]]: Chemokine (C-C motif) ligand 9
* [[CD81]]: cluster of differentiation 81
* [[MUPCDH|CDHR5]]: cadherin related family member 5
* [[COMMD9]]: COMM domain-containing protein 9
* [[CPSF7]]: Cleavage and polyadenylation specificity factor subunit 7
* [[CPT1A]]: carnitine palmitoyltransferase 1A (liver)
* [[CPT1A]]: carnitine palmitoyltransferase 1A (liver)
* [[CREB/ATF bZIP transcription factor|CREBZF]] encoding [[protein]] CREB/ATF bZIP transcription factor
* [[DAK (gene)|DAK]]: Triokinase/FMN cyclase
* [[DDI1]]: encoding [[protein]] DNA-damage inducible 1 homolog 1 (S. cerevisiae)
* [[Diacylglycerol O-acyltransferase 2|DGAT2]] encoding [[protein]] Diacylglycerol O-acyltransferase 2
* [[DHCR7]]: 7-dehydrocholesterol reductase
* [[DHCR7]]: 7-dehydrocholesterol reductase
* [[DKK3]]: Dickkopf-related protein 3
* [[DPF2]]: Double PHD fingers 2
* [[Down syndrome cell adhesion molecule like 1|DSCAML1]]: encoding [[protein]] Down syndrome cell adhesion molecule like 1
* [[EI24]]: Etoposide-induced protein 2.4 homolog
* [[FAM118B]]: encoding [[protein]] Family with sequence similarity 118, member B
* [[FAM76B]]: Family with sequence similarity 76 member B
* [[MLSTD2|FAR1]]: fatty acyl-coA reductase 1
* [[Fat atypical cadherin 3|FAT3]]: fat atypical cadherin 3
* [[FTS and Hook-interacting protein|FHIP]]: FTS and Hook-interacting protein
* [[FNBP4]]: Formin-binding protein 4
* [[GLB1L3]]: galactosidase, beta 1-like 3
* [[GLYAT]]: Glycine-N-acyltransferase
* [[Glycine-n-acyltransferase like 2|GLYATL2]] encoding [[protein]] Glycine-N-acyltransferase like 2
* [[GPHA2]]: Glycoprotein hormone alpha-2
* [[GYLTL1B]]: Glycosyltransferase-like protein LARGE2
* [[HBB]]: hemoglobin, beta
* [[HBB]]: hemoglobin, beta
* [[HBBP1]]: encoding [[protein]] Hemoglobin, beta pseudogene 1
* [[HMBS (gene)|HMBS]]: hydroxymethylbilane VIIA
* [[HMBS (gene)|HMBS]]: hydroxymethylbilane VIIA
* [[PAX6]]
* [[HRASLS3]]: adipose phospholipase A2
* [[HTATIP2]]: HIV-1 Tat interactive protein 2
* [[HYOU1]]: hypoxia upregulated protein 1
* [[Interferon induced transmembrane protein 2|IFITM2]] encoding [[protein]] Interferon induced transmembrane protein 2
* [[Intraflagellar transport protein 46 homolog|IFT46]]: intraflagellar transport protein 46 homolog
* [[Insulin gene|INS]]: insulin gene <ref>[http://ghr.nlm.nih.gov/gene/INS INS - insulin - Genetics Home Reference<!-- Bot generated title -->]</ref>
* [[KDM2A]]: lysine demethylase 2A
* [[KIAA1549L (gene)|KIAA1549L]] encoding [[protein]] KIAA1549-like
* [[LPXN]]: leupaxin
* [[Leucine rich repeat and fibronectin type iii domain containing 4|LRFN4]] encoding [[protein]] Leucine rich repeat and fibronectin type III domain containing 4
* [[MADD (gene)|MADD]]: MAP kinase-activating death domain protein
* [[MEN1]]: [[Multiple endocrine neoplasia type 1]]
* [[Microrna let-7a-2|MIRLET7A2]]: microRNA let-7a-2
* [[MMP7]]: Matrix metalloproteinases (MMP family)
* [[MOGAT2]]: monoacylglycerol O-acyltransferase 2
* [[MTRNR2L8]]: encoding [[protein]] MT-RNR2-like 8
* [[NADSYN1]]: NAD synthetase 1
* [[NAP1L4]]: nucleosome assembly protein 1-like 4
* [[NFRKB]]: nuclear factor related to kappa-B binding protein
* [[NNMT]]: nicotinamide N-methyltransferase
* [[NRGN]]: neurogranin
* [[P53AIP1]]: p53-regulated apoptosis-inducing protein 1
* [[PAX6]]: paired box 6
* [[Pecanex homolog 3|PCNX3]] encoding [[protein]] Pecanex homolog 3
* [[Pepsinogen 3, group I (pepsinogen A)|PGA3]] encoding [[protein]] Pepsinogen 3, group I (pepsinogen A)
* [[Piwi like rna-mediated gene silencing 4|PIWIL4]] encoding [[protein]] Piwi like RNA-mediated gene silencing 4
* [[Proline rich 5 like|PRR5L]]: proline rich 5 like
* [[PTPRCAP]]: protein tyrosine phosphatase receptor type C associated protein
* [[PTS (gene)|PTS]]: 6-pyruvoyltetrahydropterin synthase
* [[PTS (gene)|PTS]]: 6-pyruvoyltetrahydropterin synthase
* [[QSER1]]: glutamine serine rich protein 1
* [[RAG1]]/[[RAG2]]: recombination activating genes
* [[RELT]]: tumor necrosis factor recepteor
* [[REXO2]]: RNA exonuclease 2
* [[RNH1]]: ribonuclease inhibitor 1
* [[RNU2-2]]: encoding [[protein]] RNA, U2 small nuclear 2
* [[ROM1]]: retinal outer segment membrane protein 1
* [[60S ribosomal protein L27a|RPL27A]]: encoding [[protein]] 60S ribosomal protein L27a
* [[60S ribosomal protein L36a|RPL36A]]: encoding [[protein]] 60S ribosomal protein L36a
* [[RSF1]]: remodeling and spacing factor 1
* [[SAA1]]: serum amyloid A1
* [[SAA1]]: serum amyloid A1
* [[SAA2]]: serum amyloid A2
* [[SAC3D1]]: SAC3 domain-containing protein 1
* [[SART1]]: squamous cell carcinoma antigen recognized by T-cells 1
* [[SBF2]]: SET binding factor 2
* [[SBF2]]: SET binding factor 2
* [[SCGB1D2]]: secretoglobin family 1D member 2
* [[SESN3]] encoding [[protein]] Sestrin 3
* [[Sid1 transmembrane family member 2|SIDT2]] encoding [[protein]] SID1 transmembrane family member 2
* [[Solute carrier family 17 (vesicular glutamate transporter), member 6|SLC17A6]]: encoding [[protein]] Solute carrier family 17 (vesicular glutamate transporter), member 6
* [[SMPD1]]: sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase)
* [[SMPD1]]: sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase)
* [[SPA17]]: sperm autoantigenic protein 17
* [[Srp receptor alpha subunit|SRPRA]]: Srp receptor alpha subunit
* [[TAF1D]]: TATA box binding protein associated factor RNA polymerase 1 subunit D
* [[Transaldolase 1|TALDO1]] encoding [[protein]] Transaldolase 1
* [[TBRG1]]: transforming growth factor beta regulator 1
* [[TECTA]]: tectorin alpha (nonsyndromic deafness)
* [[TECTA]]: tectorin alpha (nonsyndromic deafness)
* [[tyrosine hydroxylase|TH]]: tyrosine hydroxylase
* [[tyrosine hydroxylase|TH]]: tyrosine hydroxylase
* [[THRSP]]: thyroid hormone inducible hepatic protein
* [[THYN1]]: thymocyte nuclear protein 1
* [[TIMM10]]: translocase of inner mitochondrial membrane 10
* [[TIMM10B]]: Mitochondrial import inner membrane translocase subunit Tim9 B
* [[TM7SF2]]: transmembrane 7 superfamily member 2
* [[TMEM109]]: encoding [[protein]] Transmembrane protein 109
* [[TMEM123]]: transmembrane protein 123
* [[TMEM126B]]: transmembrane protein 126B
* [[Transmembrane protein 134|TMEM134]]: transmembrane protein 134
* [[TMEM25]]: transmembrane protein 25
* [[TP53I11]]: tumor protein 53 inducible protein 11
* [[TRAPPC4]]: trafficking protein particle complex subunit 4
* [[TRPT1]]: tRNA 2'-phosphotransferase 1
* [[UNC93B1]]: Unc-93 homolog B1
* [[UPK2]]: uroplakin-2
* [[USH1C]]: Usher syndrome 1C (autosomal recessive, severe)
* [[USH1C]]: Usher syndrome 1C (autosomal recessive, severe)
* [[USP47]]: ubiquitin specific peptidase 47
* [[UVRAG]]: UV radiation resistance associated
* [[VPS26B]]: vacuolar protein sorting 26 homolog B
* [[VSIG2]]: V-set and immunoglobulin domain containing 2
* [[WT1]]: [[Wilms tumor]] protein
* [[YIF1A]]: Yip1 interacting factor homolog A
* [[ZFP91-CNTF]]
* [[ZNF408]]: zinc finger protein 408


==Diseases & disorders==
==Diseases and disorders==
{{wikinews|Large study provides new insights in autism's genetic code}}
{{wikinews|Large study provides new insights in autism's genetic code}}
The following diseases are some of those related to genes on chromosome 11:
The following diseases and disorders are some of those related to genes on chromosome 11:
* [[autism|autism (neurexin 1)]] [http://news.bbc.co.uk/1/hi/health/6369347.stm]
{{div col |3|colwidth=}}
* [[aniridia]]
* [[autism]] (neurexin 1) <ref>{{cite web |url=http://news.bbc.co.uk/1/hi/health/6369347.stm |title=Autism gene breakthrough hailed |format= |work=Health |publisher=BBC NEWS | date=2007-02-19 | accessdate=2010-01-02}}</ref>
* [[acute intermittent porphyria]]
* [[acute intermittent porphyria]]
* [[albinism]]
* [[ataxia-telangiectasia]]
* [[ataxia-telangiectasia]]
* [[Beckwith-Wiedemann syndrome]]
* [[Best's disease]]
* [[beta-ketothiolase deficiency]]
* [[beta-ketothiolase deficiency]]
* [[beta thalassemia]]
* [[beta thalassemia]]
Line 42: Line 198:
* [[carnitine palmitoyltransferase I deficiency]]
* [[carnitine palmitoyltransferase I deficiency]]
* [[Charcot-Marie-Tooth disease]]
* [[Charcot-Marie-Tooth disease]]
* [[Charcot-Marie-Tooth disease, type 4]]
*[[Cystic Fibrosis]]
*[[Depression (mood)|Depression]]
* [[Denys-Drash syndrome]]
* [[Denys-Drash syndrome]]
* [[familial Mediterranean fever]]
* [[familial Mediterranean fever]]
* [[Hereditary angioedema]] [[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106100]]
* [[Hereditary angioedema]] {{OMIM3|106100}}
* [[Insulinoma]]
* [[Jacobsen syndrome]]
* [[Jacobsen syndrome]]
* [[Jervell and Lange-Nielsen syndrome]]
* [[Jervell and Lange-Nielsen syndrome]]
* [[Mantle cell lymphoma]] (t11;14)
* [[Meckel syndrome]]
* [[Meckel syndrome]]
* [[methemoglobinemia, beta-globin type]]
* [[methemoglobinemia]], beta-globin type
* [[Mixed Lineage Leukemia]]
* [[multiple endocrine neoplasia type 1]]
* [[multiple endocrine neoplasia type 1]]
* [[Hereditary Multiple Exostoses]]
* [[Hereditary Multiple Exostoses]]
* [[Niemann-Pick disease]]
* [[Niemann-Pick disease]]
* [[nonsyndromic deafness]]
* [[nonsyndromic deafness]]
* [[nonsyndromic deafness, autosomal dominant]]
* [[nonsyndromic deafness, autosomal recessive]]
* [[porphyria]]
* [[porphyria]]
* [[Potocki-Shaffer syndrome|Potocki-Shaffer Syndrome]]
* [[Romano-Ward syndrome]]
* [[Romano-Ward syndrome]]
* [[sickle cell anemia]]
* [[Sickle cell anemia]]<ref>[http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/hbb.shtml Human Genome Project Information Site Has Been Updated<!-- Bot generated title -->]</ref>
* [[Smith-Lemli-Opitz syndrome]]
* [[Smith-Lemli-Opitz syndrome]]
* [[tetrahydrobiopterin deficiency]]
* [[tetrahydrobiopterin deficiency]]
* [[Usher syndrome]]
* [[Usher syndrome]]
* [[Usher syndrome type I]]
* [[WAGR syndrome]]
* [[WAGR syndrome]]
* [[Zollinger-Ellison syndrome]]
* [[Wiedemann-Steiner syndrome]]
* [[Wilms' tumor]]
{{div col end}}
 
==Cytogenetic band==
{{multiple image
| header = G-banding ideograms of human chromosome 11
| total_width = 400
| image1 = Human chromosome 11 ideogram vertical.svg
| width1 = 216
| height1= 1125
| caption1 = G-banding ideogram of human chromosome 11 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e.g. [[Ensembl]], [[UCSC Genome Browser]]).
| image2 = Human chromosome 11 - 400 550 850 bphs.png
| width2 = 1003
| height2= 2801
| caption2 = G-banding patterns of human chromosome 11 in three different resolutions (400,<ref name="400bphs">Genome Decoration Page, NCBI. [ftp://ftp.ncbi.nlm.nih.gov/pub/gdp/ideogram_9606_GCF_000001305.14_400_V1 Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3)]. Last update 2014-03-04. Retrieved 2017-04-26.</ref> 550<ref name="550bphs">Genome Decoration Page, NCBI.  [ftp://ftp.ncbi.nlm.nih.gov/pub/gdp/ideogram_9606_GCF_000001305.14_550_V1 Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3)]. Last update 2015-08-11. Retrieved 2017-04-26.</ref> and 850<ref name="850bphs">Genome Decoration Page, NCBI.  [ftp://ftp.ncbi.nlm.nih.gov/pub/gdp/ideogram_9606_GCF_000001305.14_850_V1 Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3)]. Last update 2014-06-03. Retrieved 2017-04-26.</ref>). Band length in this diagram is based on the ideograms from ISCN (2013).<ref name="Nomenclature2013">{{cite book|author=International Standing Committee on Human Cytogenetic Nomenclature|title=ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013)|url=https://books.google.com/books?id=lGCLrh0DIwEC|year=2013|publisher=Karger Medical and Scientific Publishers|isbn=978-3-318-02253-7}}</ref> This type of ideogram represents actual relative band length observed under a microscope at the different moments during the [[Mitosis|mitotic process]].<ref name="SethakulvichaiManitpornsut2012">{{cite journal|last1=Sethakulvichai|first1=W.|last2=Manitpornsut|first2=S.|last3=Wiboonrat|first3=M.|last4=Lilakiatsakun|first4=W.|last5=Assawamakin|first5=A.|last6=Tongsima|first6=S.|title=Estimation of band level resolutions of human chromosome images|year=2012|pages=276–282|journal=In Computer Science and Software Engineering (JCSSE), 2012 International Joint Conference on|doi=10.1109/JCSSE.2012.6261965|url=https://www.researchgate.net/profile/Anunchai_Assawamakin/publication/261304470_Estimation_of_band_level_resolutions_of_human_chromosome_images/links/5459f7ff0cf2cf516483fffd/Estimation-of-band-level-resolutions-of-human-chromosome-images.pdf}}</ref>
}}
{| class="wikitable" style="text-align:right"
|+ [[G banding|G-band]]s of human chromosome 11 in resolution 850 bphs<ref>Genome Decoration Page, NCBI.  [ftp://ftp.ncbi.nlm.nih.gov/pub/gdp/ideogram_9606_GCF_000001305.14_850_V1 Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3)]. Last update 2014-06-03. Retrieved 2017-04-26.</ref>
! Chr.
! Arm<ref>"'''p'''": Short arm; "'''q'''": Long arm.</ref>
! Band<ref>For cytogenetic banding nomenclature, see article [[Locus (genetics)|locus]].</ref>
! ISCN<br/>start<ref name="ISCN">These values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An International System for Human Cytogenetic Nomenclature (2013). [[Arbitrary unit]].</ref>
! ISCN<br/>stop<ref name="ISCN"/>
! Basepair<br/>start
! Basepair<br/>stop
! Stain<ref>'''gpos''': Region which is positively stained by [[G banding]], generally [[GC-content|AT-rich]] and gene poor; '''gneg''': Region which is negatively stained by G banding, generally [[GC-content|CG-rich]] and gene rich; '''acen''' [[Centromere]]. '''var''': Variable region; '''stalk''': Stalk.</ref>
! Density
|-
| 11 || p
|style="text-align:left"| 15.5 || 0 || 230 || {{val|1|fmt=commas}} || {{val|2800000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 15.4 || 230 || 461 || {{val|2800001|fmt=commas}} || {{val|11700000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || p
|style="text-align:left"| 15.3 || 461 || 745 || {{val|11700001|fmt=commas}} || {{val|13800000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 15.2 || 745 || 935 || {{val|13800001|fmt=commas}} || {{val|16900000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || p
|style="text-align:left"| 15.1 || 935 || 1246 || {{val|16900001|fmt=commas}} || {{val|22000000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 14.3 || 1246 || 1490 || {{val|22000001|fmt=commas}} || {{val|26200000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || p
|style="text-align:left"| 14.2 || 1490 || 1545 || {{val|26200001|fmt=commas}} || {{val|27200000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 14.1 || 1545 || 1775 || {{val|27200001|fmt=commas}} || {{val|31000000|fmt=commas}}
|style="background:#636363; color:white;"| gpos || 75
|-
| 11 || p
|style="text-align:left"| 13 || 1775 || 2114 || {{val|31000001|fmt=commas}} || {{val|36400000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 12 || 2114 || 2357 || {{val|36400001|fmt=commas}} || {{val|43400000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || p
|style="text-align:left"| 11.2 || 2357 || 2655 || {{val|43400001|fmt=commas}} || {{val|48800000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || p
|style="text-align:left"| 11.12 || 2655 || 2872 || {{val|48800001|fmt=commas}} || {{val|51000000|fmt=commas}}
|style="background:#636363; color:white;"| gpos || 75
|-
| 11 || p
|style="text-align:left"| 11.11 || 2872 || 3035 || {{val|51000001|fmt=commas}} || {{val|53400000|fmt=commas}}
|style="background:#6e7f8f; color:white;"| acen ||
|-
| 11 || q
|style="text-align:left"| 11 || 3035 || 3197 || {{val|53400001|fmt=commas}} || {{val|55800000|fmt=commas}}
|style="background:#6e7f8f; color:white;"| acen ||
|-
| 11 || q
|style="text-align:left"| 12.1 || 3197 || 3414 || {{val|55800001|fmt=commas}} || {{val|60100000|fmt=commas}}
|style="background:#636363; color:white;"| gpos || 75
|-
| 11 || q
|style="text-align:left"| 12.2 || 3414 || 3550 || {{val|60100001|fmt=commas}} || {{val|61900000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 12.3 || 3550 || 3685 || {{val|61900001|fmt=commas}} || {{val|63600000|fmt=commas}}
|style="background:#d9d9d9"| gpos || 25
|-
| 11 || q
|style="text-align:left"| 13.1 || 3685 || 4037 || {{val|63600001|fmt=commas}} || {{val|66100000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 13.2 || 4037 || 4186 || {{val|66100001|fmt=commas}} || {{val|68700000|fmt=commas}}
|style="background:#d9d9d9"| gpos || 25
|-
| 11 || q
|style="text-align:left"| 13.3 || 4186 || 4512 || {{val|68700001|fmt=commas}} || {{val|70500000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 13.4 || 4512 || 4688 || {{val|70500001|fmt=commas}} || {{val|75500000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || q
|style="text-align:left"| 13.5 || 4688 || 4877 || {{val|75500001|fmt=commas}} || {{val|77400000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 14.1 || 4877 || 5148 || {{val|77400001|fmt=commas}} || {{val|85900000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || q
|style="text-align:left"| 14.2 || 5148 || 5257 || {{val|85900001|fmt=commas}} || {{val|88600000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 14.3 || 5257 || 5474 || {{val|88600001|fmt=commas}} || {{val|93000000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || q
|style="text-align:left"| 21 || 5474 || 5690 || {{val|93000001|fmt=commas}} || {{val|97400000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 22.1 || 5690 || 5934 || {{val|97400001|fmt=commas}} || {{val|102300000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || q
|style="text-align:left"| 22.2 || 5934 || 6070 || {{val|102300001|fmt=commas}} || {{val|103000000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 22.3 || 6070 || 6300 || {{val|103000001|fmt=commas}} || {{val|110600000|fmt=commas}}
|style="background:black; color:white;"| gpos || 100
|-
| 11 || q
|style="text-align:left"| 23.1 || 6300 || 6503 || {{val|110600001|fmt=commas}} || {{val|112700000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 23.2 || 6503 || 6693 || {{val|112700001|fmt=commas}} || {{val|114600000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || q
|style="text-align:left"| 23.3 || 6693 || 7167 || {{val|114600001|fmt=commas}} || {{val|121300000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 24.1 || 7167 || 7316 || {{val|121300001|fmt=commas}} || {{val|124000000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || q
|style="text-align:left"| 24.2 || 7316 || 7533 || {{val|124000001|fmt=commas}} || {{val|127900000|fmt=commas}}
| style="background:white"| gneg ||
|-
| 11 || q
|style="text-align:left"| 24.3 || 7533 || 7695 || {{val|127900001|fmt=commas}} || {{val|130900000|fmt=commas}}
|style="background:#979797"| gpos || 50
|-
| 11 || q
|style="text-align:left"| 25 || 7695 || 7980 || {{val|130900001|fmt=commas}} || {{val|135086622|fmt=commas}}
| style="background:white"| gneg ||
|}


==References==
==References==
<div class="references-small">
{{reflist}}
{{reflist|2}}
{{refbegin}}
</div>
* {{cite journal | author=Gilbert F | title=Disease genes and chromosomes: disease maps of the human genome | journal=Genet Test | year=2000 | pages=409–26 | volume=4 | issue=4 | pmid=11216668 | doi=10.1089/109065700750065180}}
* {{cite journal | author=Gilbert F | title=Disease genes and chromosomes: disease maps of the human genome | journal=Genet Test | year=2000 | pages=409-26 | volume=4 | issue=4 | id=PMID 11216668}}
{{refend}}
 
{{genetics-stub}}


{{Template:Chromosomes}}
==External links==
{{Commons category|Human chromosome 11}}
* {{cite web | author= National Institutes of Health  | title= Chromosome 11 | work= Genetics Home Reference | url= http://ghr.nlm.nih.gov/chromosome=11| accessdate=2017-05-06}}
* {{Cite web|url=http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo11.shtml|title=Chromosome 11|website=Human Genome Project Information Archive 1990–2003|access-date=2017-05-06}}


[[Category:Chromosomes]]
{{Chromosomes}}
{{Chromosome genetics}}


[[ca:Cromosoma 11]]
[[Category:Chromosomes (human)|Chromosome 11]]
[[fr:Chromosome 11 humain]]
[[Category:Genes on human chromosome 11|*]]
[[it:Cromosoma 11 (umano)]]
[[hu:Humán 11-es kromoszóma]]
[[no:Kromosom 11]]
[[pl:Chromosom 11]]
[[pt:Cromossoma 11 (humano)]]
[[sr:Хромозом 11 (човек)]]
[[tr:Kromozom 11]]
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Latest revision as of 12:52, 29 November 2017

Chromosome 11 (human)
File:Human male karyotpe high resolution - Chromosome 11 cropped.png
Human chromosome 11 pair after G-banding.
One is from mother, one is from father.
File:Human male karyotpe high resolution - Chromosome 11.png
Chromosome 11 pair
in human male karyogram.
Features
Length (bp)135,086,622 bp
(GRCh38)[1]
No. of genes1,224 (CCDS)
TypeAutosome
Centromere positionSubmetacentric[2]
(53.4 Mbp[3])
Complete gene lists
CCDS?
HGNC?
UniProt?
NCBI?
External map viewers
EnsemblChromosome 11
EntrezChromosome 11
NCBIChromosome 11
UCSCChromosome 11
Full DNA sequences
RefSeqNC_000011 (FASTA)
GenBankCM000673 (FASTA)

Chromosome 11 is one of the 23 pairs of chromosomes in humans. Humans normally have two copies of this chromosome. Chromosome 11 spans about 135 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells.

At 21.5 genes per megabase, Chromosome 11 is one of the most gene-rich, and disease-rich, chromosomes in the human genome.

More than 40% of the 856 olfactory receptor genes in the human genome are located in 28 single-gene, and multi-gene, clusters along this chromosome.

Genes

See also: Category:Genes on human chromosome 11.

The following are some of the gene count estimates of human chromosome 11. Because researchers use different approaches to genome annotation their predictions of the number of genes on each chromosome varies (for technical details, see gene prediction). Among various projects, the collaborative consensus coding sequence project (CCDS) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.[4]

Estimated by Protein-coding genes Non-coding RNA genes Pseudogenes Source Release date
CCDS 1,224 - - [5] 2016-09-08
HGNC 1,262 271 666 [6] 2017-05-12
Ensembl 1,301 1,060 811 [7] 2017-03-29
NCBI 1,314 860 839 [8][9][10] 2017-05-19

The following are some of the genes located on chromosome 11:

  • ACAT1: acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)
  • ACRV1: encoding protein Acrosomal protein SP-10
  • AKIP1: A kinase interacting protein 1
  • ALKBH3 encoding protein AlkB homolog 3, alpha-ketoglutaratedependent dioxygenase
  • AMOTL1: angiomotin-like protein 1
  • AMPD3: encoding enzyme AMP deaminase 3
  • API5: encoding protein Apoptosis inhibitor 5
  • APLNR: Apelin receptor (APJ receptor)
  • APOA4: apolipoprotein A-IV
  • ARCN1 encoding protein Archain 1
  • ASRGL1: encoding enzyme L-asparaginase
  • ATM: ataxia telangiectasia mutated (includes complementation groups A, C and D)
  • B3GNT1: encoding enzyme N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase
  • BDNF: secretes BDNF, a member of the Neurotrophin family of proteins
  • C11orf1: encoding protein
  • C11orf16: encoding protein Uncharacterized protein C11orf16
  • C11orf49: encoding protein UPF0705 protein C11orf49
  • C11orf52 encoding protein C11orf52
  • C11orf54: encoding protein Ester hydrolase C11orf54
  • C11orf58: small acidic protein
  • C11orf73: chromosome 11, open reading frame 73
  • C11orf86: encoding protein Uncharacterized protein C11orf86
  • C1QTNF4 encoding protein C1q and tumor necrosis factor related protein 4
  • C1QTNF5: encoding protein C1q and tumor necrosis factor related protein 5
  • CAPRIN1: encoding protein, cell cycle associated protein 1
  • CCDC90B: coiled coil domain containing 90B
  • CCL9: Chemokine (C-C motif) ligand 9
  • CD81: cluster of differentiation 81
  • CDHR5: cadherin related family member 5
  • COMMD9: COMM domain-containing protein 9
  • CPSF7: Cleavage and polyadenylation specificity factor subunit 7
  • CPT1A: carnitine palmitoyltransferase 1A (liver)
  • CREBZF encoding protein CREB/ATF bZIP transcription factor
  • DAK: Triokinase/FMN cyclase
  • DDI1: encoding protein DNA-damage inducible 1 homolog 1 (S. cerevisiae)
  • DGAT2 encoding protein Diacylglycerol O-acyltransferase 2
  • DHCR7: 7-dehydrocholesterol reductase
  • DKK3: Dickkopf-related protein 3
  • DPF2: Double PHD fingers 2
  • DSCAML1: encoding protein Down syndrome cell adhesion molecule like 1
  • EI24: Etoposide-induced protein 2.4 homolog
  • FAM118B: encoding protein Family with sequence similarity 118, member B
  • FAM76B: Family with sequence similarity 76 member B
  • FAR1: fatty acyl-coA reductase 1
  • FAT3: fat atypical cadherin 3
  • FHIP: FTS and Hook-interacting protein
  • FNBP4: Formin-binding protein 4
  • GLB1L3: galactosidase, beta 1-like 3
  • GLYAT: Glycine-N-acyltransferase
  • GLYATL2 encoding protein Glycine-N-acyltransferase like 2
  • GPHA2: Glycoprotein hormone alpha-2
  • GYLTL1B: Glycosyltransferase-like protein LARGE2
  • HBB: hemoglobin, beta
  • HBBP1: encoding protein Hemoglobin, beta pseudogene 1
  • HMBS: hydroxymethylbilane VIIA
  • HRASLS3: adipose phospholipase A2
  • HTATIP2: HIV-1 Tat interactive protein 2
  • HYOU1: hypoxia upregulated protein 1
  • IFITM2 encoding protein Interferon induced transmembrane protein 2
  • IFT46: intraflagellar transport protein 46 homolog
  • INS: insulin gene [11]
  • KDM2A: lysine demethylase 2A
  • KIAA1549L encoding protein KIAA1549-like
  • LPXN: leupaxin
  • LRFN4 encoding protein Leucine rich repeat and fibronectin type III domain containing 4
  • MADD: MAP kinase-activating death domain protein
  • MEN1: Multiple endocrine neoplasia type 1
  • MIRLET7A2: microRNA let-7a-2
  • MMP7: Matrix metalloproteinases (MMP family)
  • MOGAT2: monoacylglycerol O-acyltransferase 2
  • MTRNR2L8: encoding protein MT-RNR2-like 8
  • NADSYN1: NAD synthetase 1
  • NAP1L4: nucleosome assembly protein 1-like 4
  • NFRKB: nuclear factor related to kappa-B binding protein
  • NNMT: nicotinamide N-methyltransferase
  • NRGN: neurogranin
  • P53AIP1: p53-regulated apoptosis-inducing protein 1
  • PAX6: paired box 6
  • PCNX3 encoding protein Pecanex homolog 3
  • PGA3 encoding protein Pepsinogen 3, group I (pepsinogen A)
  • PIWIL4 encoding protein Piwi like RNA-mediated gene silencing 4
  • PRR5L: proline rich 5 like
  • PTPRCAP: protein tyrosine phosphatase receptor type C associated protein
  • PTS: 6-pyruvoyltetrahydropterin synthase
  • QSER1: glutamine serine rich protein 1
  • RAG1/RAG2: recombination activating genes
  • RELT: tumor necrosis factor recepteor
  • REXO2: RNA exonuclease 2
  • RNH1: ribonuclease inhibitor 1
  • RNU2-2: encoding protein RNA, U2 small nuclear 2
  • ROM1: retinal outer segment membrane protein 1
  • RPL27A: encoding protein 60S ribosomal protein L27a
  • RPL36A: encoding protein 60S ribosomal protein L36a
  • RSF1: remodeling and spacing factor 1
  • SAA1: serum amyloid A1
  • SAA2: serum amyloid A2
  • SAC3D1: SAC3 domain-containing protein 1
  • SART1: squamous cell carcinoma antigen recognized by T-cells 1
  • SBF2: SET binding factor 2
  • SCGB1D2: secretoglobin family 1D member 2
  • SESN3 encoding protein Sestrin 3
  • SIDT2 encoding protein SID1 transmembrane family member 2
  • SLC17A6: encoding protein Solute carrier family 17 (vesicular glutamate transporter), member 6
  • SMPD1: sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase)
  • SPA17: sperm autoantigenic protein 17
  • SRPRA: Srp receptor alpha subunit
  • TAF1D: TATA box binding protein associated factor RNA polymerase 1 subunit D
  • TALDO1 encoding protein Transaldolase 1
  • TBRG1: transforming growth factor beta regulator 1
  • TECTA: tectorin alpha (nonsyndromic deafness)
  • TH: tyrosine hydroxylase
  • THRSP: thyroid hormone inducible hepatic protein
  • THYN1: thymocyte nuclear protein 1
  • TIMM10: translocase of inner mitochondrial membrane 10
  • TIMM10B: Mitochondrial import inner membrane translocase subunit Tim9 B
  • TM7SF2: transmembrane 7 superfamily member 2
  • TMEM109: encoding protein Transmembrane protein 109
  • TMEM123: transmembrane protein 123
  • TMEM126B: transmembrane protein 126B
  • TMEM134: transmembrane protein 134
  • TMEM25: transmembrane protein 25
  • TP53I11: tumor protein 53 inducible protein 11
  • TRAPPC4: trafficking protein particle complex subunit 4
  • TRPT1: tRNA 2'-phosphotransferase 1
  • UNC93B1: Unc-93 homolog B1
  • UPK2: uroplakin-2
  • USH1C: Usher syndrome 1C (autosomal recessive, severe)
  • USP47: ubiquitin specific peptidase 47
  • UVRAG: UV radiation resistance associated
  • VPS26B: vacuolar protein sorting 26 homolog B
  • VSIG2: V-set and immunoglobulin domain containing 2
  • WT1: Wilms tumor protein
  • YIF1A: Yip1 interacting factor homolog A
  • ZFP91-CNTF
  • ZNF408: zinc finger protein 408

Diseases and disorders

The following diseases and disorders are some of those related to genes on chromosome 11:

Cytogenetic band

G-banding ideograms of human chromosome 11
File:Human chromosome 11 ideogram vertical.svg
G-banding ideogram of human chromosome 11 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e.g. Ensembl, UCSC Genome Browser).
File:Human chromosome 11 - 400 550 850 bphs.png
G-banding patterns of human chromosome 11 in three different resolutions (400,[14] 550[15] and 850[3]). Band length in this diagram is based on the ideograms from ISCN (2013).[16] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process.[17]
G-bands of human chromosome 11 in resolution 850 bphs[18]
Chr. Arm[19] Band[20] ISCN
start[21] 		ISCN
stop[21] 		Basepair
start 		Basepair
stop 		Stain[22] Density
11 p 15.5 0 230 1 2,800,000 gneg
11 p 15.4 230 461 2,800,001 11,700,000 gpos 50
11 p 15.3 461 745 11,700,001 13,800,000 gneg
11 p 15.2 745 935 13,800,001 16,900,000 gpos 50
11 p 15.1 935 1246 16,900,001 22,000,000 gneg
11 p 14.3 1246 1490 22,000,001 26,200,000 gpos 100
11 p 14.2 1490 1545 26,200,001 27,200,000 gneg
11 p 14.1 1545 1775 27,200,001 31,000,000 gpos 75
11 p 13 1775 2114 31,000,001 36,400,000 gneg
11 p 12 2114 2357 36,400,001 43,400,000 gpos 100
11 p 11.2 2357 2655 43,400,001 48,800,000 gneg
11 p 11.12 2655 2872 48,800,001 51,000,000 gpos 75
11 p 11.11 2872 3035 51,000,001 53,400,000 acen
11 q 11 3035 3197 53,400,001 55,800,000 acen
11 q 12.1 3197 3414 55,800,001 60,100,000 gpos 75
11 q 12.2 3414 3550 60,100,001 61,900,000 gneg
11 q 12.3 3550 3685 61,900,001 63,600,000 gpos 25
11 q 13.1 3685 4037 63,600,001 66,100,000 gneg
11 q 13.2 4037 4186 66,100,001 68,700,000 gpos 25
11 q 13.3 4186 4512 68,700,001 70,500,000 gneg
11 q 13.4 4512 4688 70,500,001 75,500,000 gpos 50
11 q 13.5 4688 4877 75,500,001 77,400,000 gneg
11 q 14.1 4877 5148 77,400,001 85,900,000 gpos 100
11 q 14.2 5148 5257 85,900,001 88,600,000 gneg
11 q 14.3 5257 5474 88,600,001 93,000,000 gpos 100
11 q 21 5474 5690 93,000,001 97,400,000 gneg
11 q 22.1 5690 5934 97,400,001 102,300,000 gpos 100
11 q 22.2 5934 6070 102,300,001 103,000,000 gneg
11 q 22.3 6070 6300 103,000,001 110,600,000 gpos 100
11 q 23.1 6300 6503 110,600,001 112,700,000 gneg
11 q 23.2 6503 6693 112,700,001 114,600,000 gpos 50
11 q 23.3 6693 7167 114,600,001 121,300,000 gneg
11 q 24.1 7167 7316 121,300,001 124,000,000 gpos 50
11 q 24.2 7316 7533 124,000,001 127,900,000 gneg
11 q 24.3 7533 7695 127,900,001 130,900,000 gpos 50
11 q 25 7695 7980 130,900,001 135,086,622 gneg

References

  1. ↑ "Human Genome Assembly GRCh38 - Genome Reference Consortium". National Center for Biotechnology Information. 2013-12-24. Retrieved 2017-03-04.
  2. ↑ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
  3. ↑ 3.0 3.1 Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
  4. ↑ Pertea M, Salzberg SL (2010). "Between a chicken and a grape: estimating the number of human genes". Genome Biol. 11 (5): 206. doi:10.1186/gb-2010-11-5-206. PMC 2898077. PMID 20441615.
  5. ↑ "Search results - 11[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene". NCBI. CCDS Release 20 for Homo sapiens. 2016-09-08. Retrieved 2017-05-28.
  6. ↑ "Statistics & Downloads for chromosome 11". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.
  7. ↑ "Chromosome 11: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19.
  8. ↑ "Search results - 11[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  9. ↑ "Search results - 11[CHR] AND "Homo sapiens"[Organism] AND ( ("genetype miscrna"[Properties] OR "genetype ncrna"[Properties] OR "genetype rrna"[Properties] OR "genetype trna"[Properties] OR "genetype scrna"[Properties] OR "genetype snrna"[Properties] OR "genetype snorna"[Properties]) NOT "genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  10. ↑ "Search results - 11[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  11. ↑ INS - insulin - Genetics Home Reference
  12. ↑ "Autism gene breakthrough hailed". Health. BBC NEWS. 2007-02-19. Retrieved 2010-01-02.
  13. ↑ Human Genome Project Information Site Has Been Updated
  14. ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
  15. ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
  16. ↑ International Standing Committee on Human Cytogenetic Nomenclature (2013). ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013). Karger Medical and Scientific Publishers. ISBN 978-3-318-02253-7.
  17. ↑ Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012). "Estimation of band level resolutions of human chromosome images" (PDF). In Computer Science and Software Engineering (JCSSE), 2012 International Joint Conference on: 276–282. doi:10.1109/JCSSE.2012.6261965.
  18. ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
  19. ↑ "p": Short arm; "q": Long arm.
  20. ↑ For cytogenetic banding nomenclature, see article locus.
  21. ↑ 21.0 21.1 These values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An International System for Human Cytogenetic Nomenclature (2013). Arbitrary unit.
  22. ↑ gpos: Region which is positively stained by G banding, generally AT-rich and gene poor; gneg: Region which is negatively stained by G banding, generally CG-rich and gene rich; acen Centromere. var: Variable region; stalk: Stalk.

External links

  • National Institutes of Health. "Chromosome 11". Genetics Home Reference. Retrieved 2017-05-06.
  • "Chromosome 11". Human Genome Project Information Archive 1990–2003. Retrieved 2017-05-06.
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