Biology:Chromosome 10
Chromosome 10 | |
---|---|
Human chromosome 10 pair after G-banding. One is from mother, one is from father. | |
Chromosome 10 pair in human male karyogram. | |
Features | |
Length (bp) | 134,758,134 bp (CHM13) |
No. of genes | 706 (CCDS)[1] |
Type | Autosome |
Centromere position | Submetacentric[2] (39.8 Mbp[3]) |
Complete gene lists | |
CCDS | Gene list |
HGNC | Gene list |
UniProt | Gene list |
NCBI | Gene list |
External map viewers | |
Ensembl | Chromosome 10 |
Entrez | Chromosome 10 |
NCBI | Chromosome 10 |
UCSC | Chromosome 10 |
Full DNA sequences | |
RefSeq | NC_000010 (FASTA) |
GenBank | CM000672 (FASTA) |
Chromosome 10 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 10 spans about 134 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells.
Genes
Number of genes
The following are some of the gene count estimates of human chromosome 10. 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 | 706 | — | — | [1] | 2016-09-08 |
HGNC | 708 | 244 | 614 | [5] | 2017-05-12 |
Ensembl | 728 | 881 | 568 | [6] | 2017-03-29 |
UniProt | 750 | — | — | [7] | 2018-02-28 |
NCBI | 754 | 842 | 654 | [8][9][10] | 2017-05-19 |
Gene list
The following is a partial list of genes on human chromosome 10. For complete list, see the link in the infobox on the right.
Diseases and disorders
The following diseases are related to genes on chromosome 10:
- Apert syndrome
- Barakat syndrome
- Beare–Stevenson cutis gyrata syndrome
- Charcot–Marie–Tooth disease
- Cockayne syndrome
- Congenital erythropoietic porphyria
- Cowden syndrome
- Crouzon syndrome
- Genitopatellar syndrome
- Glioblastoma multiforme
- HADDS syndrome
- Hermansky–Pudlak syndrome
- Hirschprung disease
- Jackson–Weiss syndrome
- Multiple endocrine neoplasia type 2
- Nonsyndromic deafness
- Pfeiffer syndrome
- Porphyria
- Spondyloepimetaphyseal dysplasia, Pakistani type
- Tetrahydrobiopterin deficiency
- Thiel–Behnke corneal dystrophy
- Usher syndrome
- Wolman syndrome
- Young-Simpson syndrome
Cytogenetic band
Chr. | Arm[16] | Band[17] | ISCN start[18] |
ISCN stop[18] |
Basepair start |
Basepair stop |
Stain[19] | Density |
---|---|---|---|---|---|---|---|---|
10 | p | 15.3 | 0 | 229 | 1 | 3,000,000 | gneg | |
10 | p | 15.2 | 229 | 329 | 3,000,001 | 3,800,000 | gpos | 25 |
10 | p | 15.1 | 329 | 630 | 3,800,001 | 6,600,000 | gneg | |
10 | p | 14 | 630 | 917 | 6,600,001 | 12,200,000 | gpos | 75 |
10 | p | 13 | 917 | 1175 | 12,200,001 | 17,300,000 | gneg | |
10 | p | 12.33 | 1175 | 1361 | 17,300,001 | 18,300,000 | gpos | 75 |
10 | p | 12.32 | 1361 | 1432 | 18,300,001 | 18,400,000 | gneg | |
10 | p | 12.31 | 1432 | 1604 | 18,400,001 | 22,300,000 | gpos | 75 |
10 | p | 12.2 | 1604 | 1662 | 22,300,001 | 24,300,000 | gneg | |
10 | p | 12.1 | 1662 | 1891 | 24,300,001 | 29,300,000 | gpos | 50 |
10 | p | 11.23 | 1891 | 2063 | 29,300,001 | 31,100,000 | gneg | |
10 | p | 11.22 | 2063 | 2235 | 31,100,001 | 34,200,000 | gpos | 25 |
10 | p | 11.21 | 2235 | 2406 | 34,200,001 | 38,000,000 | gneg | |
10 | p | 11.1 | 2406 | 2621 | 38,000,001 | 39,800,000 | acen | |
10 | q | 11.1 | 2621 | 2850 | 39,800,001 | 41,600,000 | acen | |
10 | q | 11.21 | 2850 | 3051 | 41,600,001 | 45,500,000 | gneg | |
10 | q | 11.22 | 3051 | 3252 | 45,500,001 | 48,600,000 | gpos | 25 |
10 | q | 11.23 | 3252 | 3409 | 48,600,001 | 51,100,000 | gneg | |
10 | q | 21.1 | 3409 | 3753 | 51,100,001 | 59,400,000 | gpos | 100 |
10 | q | 21.2 | 3753 | 3839 | 59,400,001 | 62,800,000 | gneg | |
10 | q | 21.3 | 3839 | 4097 | 62,800,001 | 68,800,000 | gpos | 100 |
10 | q | 22.1 | 4097 | 4469 | 68,800,001 | 73,100,000 | gneg | |
10 | q | 22.2 | 4469 | 4655 | 73,100,001 | 75,900,000 | gpos | 50 |
10 | q | 22.3 | 4655 | 4970 | 75,900,001 | 80,300,000 | gneg | |
10 | q | 23.1 | 4970 | 5200 | 80,300,001 | 86,100,000 | gpos | 100 |
10 | q | 23.2 | 5200 | 5331 | 86,100,001 | 87,700,000 | gneg | |
10 | q | 23.31 | 5331 | 5558 | 87,700,001 | 91,100,000 | gpos | 75 |
10 | q | 23.32 | 5558 | 5672 | 91,100,001 | 92,300,000 | gneg | |
10 | q | 23.33 | 5672 | 5887 | 92,300,001 | 95,300,000 | gpos | 50 |
10 | q | 24.1 | 5887 | 5973 | 95,300,001 | 97,500,000 | gneg | |
10 | q | 24.2 | 5973 | 6131 | 97,500,001 | 100,100,000 | gpos | 50 |
10 | q | 24.31 | 6131 | 6202 | 100,100,001 | 101,200,000 | gneg | |
10 | q | 24.32 | 6202 | 6317 | 101,200,001 | 103,100,000 | gpos | 25 |
10 | q | 24.33 | 6317 | 6374 | 103,100,001 | 104,000,000 | gneg | |
10 | q | 25.1 | 6374 | 6646 | 104,000,001 | 110,100,000 | gpos | 100 |
10 | q | 25.2 | 6646 | 6761 | 110,100,001 | 113,100,000 | gneg | |
10 | q | 25.3 | 6761 | 6890 | 113,100,001 | 117,300,000 | gpos | 75 |
10 | q | 26.11 | 6890 | 7090 | 117,300,001 | 119,900,000 | gneg | |
10 | q | 26.12 | 7090 | 7219 | 119,900,001 | 121,400,000 | gpos | 50 |
10 | q | 26.13 | 7219 | 7506 | 121,400,001 | 125,700,000 | gneg | |
10 | q | 26.2 | 7506 | 7721 | 125,700,001 | 128,800,000 | gpos | 50 |
10 | q | 26.3 | 7721 | 8050 | 128,800,001 | 133,797,422 | gneg |
References
- ↑ 1.0 1.1 "Search results - 10[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene". 2016-09-08. https://www.ncbi.nlm.nih.gov/gene?term=10%5BChr%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22has%20ccds%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2. https://books.google.com/books?id=dSwWBAAAQBAJ&pg=PA45.
- ↑ 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.
- ↑ 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. PMID 20441615.
- ↑ "Statistics & Downloads for chromosome 10". 2017-05-12. https://www.genenames.org/cgi-bin/statistics?c=10.
- ↑ "Chromosome 10: Chromosome summary - Homo sapiens". 2017-03-29. http://mar2017.archive.ensembl.org/Homo_sapiens/Location/Chromosome?r=10.
- ↑ "Human chromosome 10: entries, gene names and cross-references to MIM". 2018-02-28. https://www.uniprot.org/docs/humchr10.txt.
- ↑ "Search results - 10[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=10%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.
- ↑ "Search results - 10[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". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=10%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.
- ↑ "Search results - 10[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=10%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20pseudo%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
- ↑ 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. https://books.google.com/books?id=lGCLrh0DIwEC.
- ↑ Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012). "Estimation of band level resolutions of human chromosome images". 2012 Ninth International Conference on Computer Science and Software Engineering (JCSSE). pp. 276–282. doi:10.1109/JCSSE.2012.6261965. ISBN 978-1-4673-1921-8. https://www.researchgate.net/publication/261304470.
- ↑ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
- ↑ "p": Short arm; "q": Long arm.
- ↑ For cytogenetic banding nomenclature, see article locus.
- ↑ 18.0 18.1 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.
- ↑ 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.
- "The DNA sequence and comparative analysis of human chromosome 10". Nature 429 (6990): 375–81. 2004. doi:10.1038/nature02462. PMID 15164054. Bibcode: 2004Natur.429..375D.
- "Report of the third international workshop on human chromosome 10 mapping and sequencing 1999". Cytogenet Cell Genet 90 (1–2): 1–12. 2000. doi:10.1159/000015653. PMID 11060438.
- Gilbert F (2001). "Chromosome 10". Genet Test 5 (1): 69–82. doi:10.1089/109065701750168824. PMID 11336406.
External links
- National Institutes of Health. "Chromosome 10". Genetics Home Reference. http://ghr.nlm.nih.gov/chromosome=10.
- "Chromosome 10". http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo10.shtml.
Original source: https://en.wikipedia.org/wiki/Chromosome 10.
Read more |