Biology:Chromosome 12
Chromosome 12 | |
---|---|
Human chromosome 12 pair after G-banding. One is from mother, one is from father. | |
Chromosome 12 pair in human male karyogram. | |
Features | |
Length (bp) | 133,324,548 bp (CHM13) |
No. of genes | 988 (CCDS)[1] |
Type | Autosome |
Centromere position | Submetacentric[2] (35.5 Mbp[3]) |
Complete gene lists | |
CCDS | Gene list |
HGNC | Gene list |
UniProt | Gene list |
NCBI | Gene list |
External map viewers | |
Ensembl | Chromosome 12 |
Entrez | Chromosome 12 |
NCBI | Chromosome 12 |
UCSC | Chromosome 12 |
Full DNA sequences | |
RefSeq | NC_000012 (FASTA) |
GenBank | CM000674 (FASTA) |
Chromosome 12 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 12 spans about 133 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells.
Chromosome 12 contains the Homeobox C gene cluster.
Genes
Number of genes
The following are some of the gene count estimates of human chromosome 12. 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 | 988 | — | — | [1] | 2016-09-08 |
HGNC | 995 | 318 | 545 | [5] | 2017-05-12 |
Ensembl | 1,033 | 1,202 | 617 | [6] | 2017-03-29 |
UniProt | 1,032 | — | — | [7] | 2018-02-28 |
NCBI | 1,036 | 853 | 693 | [8][9][10] | 2017-05-19 |
Gene list
The following is a partial list of genes on human chromosome 12. For complete list, see the link in the infobox on the right.
Diseases and disorders
The following diseases are some of those related to genes on chromosome 12:
- achondrogenesis type 2
- collagenopathy, types II and XI
- cornea plana 2
- episodic ataxia
- hereditary hemorrhagic telangiectasia
- hypochondrogenesis
- ichthyosis bullosa of Siemens
- Kniest dysplasia
- Kabuki syndrome
- maturity onset diabetes of the young type 3
- methylmalonic acidemia
- narcolepsy
- nonsyndromic deafness
- Noonan syndrome
- Parkinson disease
- Pallister-Killian syndrome (tetrasomy 12p)
- phenylketonuria
- spondyloepimetaphyseal dysplasia, Strudwick type
- spondyloepiphyseal dysplasia congenita
- spondyloperipheral dysplasia
- Stickler syndrome, (COL2A1-related)
- Stuttering[11]
- Triose Phosphate Isomerase deficiency
- tyrosinemia
- Von Willebrand Disease
Cytogenetic band
Chr. | Arm[16] | Band[17] | ISCN start[18] |
ISCN stop[18] |
Basepair start |
Basepair stop |
Stain[19] | Density |
---|---|---|---|---|---|---|---|---|
12 | p | 13.33 | 0 | 216 | 1 | 3,200,000 | gneg | |
12 | p | 13.32 | 216 | 345 | 3,200,001 | 5,300,000 | gpos | 25 |
12 | p | 13.31 | 345 | 633 | 5,300,001 | 10,000,000 | gneg | |
12 | p | 13.2 | 633 | 806 | 10,000,001 | 12,600,000 | gpos | 75 |
12 | p | 13.1 | 806 | 921 | 12,600,001 | 14,600,000 | gneg | |
12 | p | 12.3 | 921 | 1195 | 14,600,001 | 19,800,000 | gpos | 100 |
12 | p | 12.2 | 1195 | 1252 | 19,800,001 | 21,100,000 | gneg | |
12 | p | 12.1 | 1252 | 1526 | 21,100,001 | 26,300,000 | gpos | 100 |
12 | p | 11.23 | 1526 | 1655 | 26,300,001 | 27,600,000 | gneg | |
12 | p | 11.22 | 1655 | 1785 | 27,600,001 | 30,500,000 | gpos | 50 |
12 | p | 11.21 | 1785 | 1900 | 30,500,001 | 33,200,000 | gneg | |
12 | p | 11.1 | 1900 | 2015 | 33,200,001 | 35,500,000 | acen | |
12 | q | 11 | 2015 | 2116 | 35,500,001 | 37,800,000 | acen | |
12 | q | 12 | 2116 | 2562 | 37,800,001 | 46,000,000 | gpos | 100 |
12 | q | 13.11 | 2562 | 2706 | 46,000,001 | 48,700,000 | gneg | |
12 | q | 13.12 | 2706 | 2850 | 48,700,001 | 51,100,000 | gpos | 25 |
12 | q | 13.13 | 2850 | 3210 | 51,100,001 | 54,500,000 | gneg | |
12 | q | 13.2 | 3210 | 3383 | 54,500,001 | 56,200,000 | gpos | 25 |
12 | q | 13.3 | 3383 | 3498 | 56,200,001 | 57,700,000 | gneg | |
12 | q | 14.1 | 3498 | 3700 | 57,700,001 | 62,700,000 | gpos | 75 |
12 | q | 14.2 | 3700 | 3786 | 62,700,001 | 64,700,000 | gneg | |
12 | q | 14.3 | 3786 | 3959 | 64,700,001 | 67,300,000 | gpos | 50 |
12 | q | 15 | 3959 | 4203 | 67,300,001 | 71,100,000 | gneg | |
12 | q | 21.1 | 4203 | 4362 | 71,100,001 | 75,300,000 | gpos | 75 |
12 | q | 21.2 | 4362 | 4549 | 75,300,001 | 79,900,000 | gneg | |
12 | q | 21.31 | 4549 | 4837 | 79,900,001 | 86,300,000 | gpos | 100 |
12 | q | 21.32 | 4837 | 4894 | 86,300,001 | 88,600,000 | gneg | |
12 | q | 21.33 | 4894 | 5125 | 88,600,001 | 92,200,000 | gpos | 100 |
12 | q | 22 | 5125 | 5355 | 92,200,001 | 95,800,000 | gneg | |
12 | q | 23.1 | 5355 | 5571 | 95,800,001 | 101,200,000 | gpos | 75 |
12 | q | 23.2 | 5571 | 5643 | 101,200,001 | 103,500,000 | gneg | |
12 | q | 23.3 | 5643 | 5873 | 103,500,001 | 108,600,000 | gpos | 50 |
12 | q | 24.11 | 5873 | 6104 | 108,600,001 | 111,300,000 | gneg | |
12 | q | 24.12 | 6104 | 6219 | 111,300,001 | 111,900,000 | gpos | 25 |
12 | q | 24.13 | 6219 | 6334 | 111,900,001 | 113,900,000 | gneg | |
12 | q | 24.21 | 6334 | 6478 | 113,900,001 | 116,400,000 | gpos | 50 |
12 | q | 24.22 | 6478 | 6579 | 116,400,001 | 117,700,000 | gneg | |
12 | q | 24.23 | 6579 | 6737 | 117,700,001 | 120,300,000 | gpos | 50 |
12 | q | 24.31 | 6737 | 7083 | 120,300,001 | 125,400,000 | gneg | |
12 | q | 24.32 | 7083 | 7255 | 125,400,001 | 128,700,000 | gpos | 50 |
12 | q | 24.33 | 7255 | 7500 | 128,700,001 | 133,275,309 | gneg |
References
- ↑ 1.0 1.1 "Search results - 12[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene". 2016-09-08. https://www.ncbi.nlm.nih.gov/gene?term=12%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 3.2 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 12". 2017-05-12. https://www.genenames.org/cgi-bin/statistics?c=12.
- ↑ "Chromosome 12: Chromosome summary - Homo sapiens". 2017-03-29. http://mar2017.archive.ensembl.org/Homo_sapiens/Location/Chromosome?r=12.
- ↑ "Human chromosome 12: entries, gene names and cross-references to MIM". 2018-02-28. https://www.uniprot.org/docs/humchr12.txt.
- ↑ "Search results - 12[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=12%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 - 12[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=12%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 - 12[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". 2017-05-19. https://www.ncbi.nlm.nih.gov/gene?term=12%5BCHR%5D%20AND%20%22Homo%20sapiens%22%5BOrganism%5D%20AND%20%28%22genetype%20pseudo%22%5BProperties%5D%20AND%20alive%5Bprop%5D%29&cmd=DetailsSearch.
- ↑ Riaz N; Steinberg S; Ahmad J et al. (April 2005). "Genomewide significant linkage to stuttering on chromosome 12". Am. J. Hum. Genet. 76 (4): 647–51. doi:10.1086/429226. PMID 15714404.
- ↑ 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.
- ↑ "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.
- "Disease genes and chromosomes: disease maps of the human genome.Chromosome 12". Genet Test 4 (3): 319–33. 2000. doi:10.1089/10906570050501588. PMID 11142767.
- "A high-resolution map of human chromosome 12". Nature 409 (6822): 945–6. 2001. doi:10.1038/35057174. PMID 11237017. Bibcode: 2001Natur.409..945M.
External links
- National Institutes of Health. "Chromosome 12". Genetics Home Reference. http://ghr.nlm.nih.gov/chromosome=12.
- "Chromosome 12". http://web.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/chromo12.shtml.
Original source: https://en.wikipedia.org/wiki/Chromosome 12.
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