Chromosome 9 Explained
Length Bp: | 150,617,247 bp (CHM13) |
Genes: | 739 (CCDS) |
Type: | Autosome |
Centromere Position: | Submetacentric[1] (43.0 Mbp[2]) |
Chr: | 9 |
Ensembl Id: | 9 |
Entrez Id: | 9 |
Ncbi Id: | 9 |
Ucsc Id: | 9 |
Refseq Id: | NC_000009 |
Genbank Id: | CM000671 |
Chromosome 9 is one of the 23 pairs of chromosomes in humans. Humans normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 150 million base pairs of nucleic acids (the building blocks of DNA) and represents between 4.0 and 4.5% of the total DNA in cells.
Genes
Number of genes
These are some of the gene count estimates of human chromosome 9. 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.[3]
Gene list
The following is a partial list of genes on human chromosome 9. For a 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 9:
Cytogenetic band
G-bands of human chromosome 9 in resolution 850 bphs[11] ! Chr. ! Arm[12] ! Band[13] ! ISCN
start[14] ! ISCN
stop! Basepair
start ! Basepair
stop ! Stain[15] ! Density9 | p | 24.3 | 0 | 127 | | | gneg | |
9 | p | 24.2 | 127 | 268 | | | gpos | 25 |
9 | p | 24.1 | 268 | 451 | | | gneg | |
9 | p | 23 | 451 | 677 | | | gpos | 75 |
9 | p | 22.3 | 677 | 846 | | | gneg | |
9 | p | 22.2 | 846 | 987 | | | gpos | 25 |
9 | p | 22.1 | 987 | 1085 | | | gneg | |
9 | p | 21.3 | 1085 | 1297 | | | gpos | 100 |
9 | p | 21.2 | 1297 | 1395 | | | gneg | |
9 | p | 21.1 | 1395 | 1621 | | | gpos | 100 |
9 | p | 13.3 | 1621 | 1917 | | | gneg | |
9 | p | 13.2 | 1917 | 2030 | | | gpos | 25 |
9 | p | 13.1 | 2030 | 2171 | | | gneg | |
9 | p | 12 | 2171 | 2312 | | | gpos | 50 |
9 | p | 11.2 | 2312 | 2523 | | | gneg | |
9 | p | 11.1 | 2523 | 2650 | | | acen | |
9 | q | 11 | 2650 | 2876 | | | acen | |
9 | q | 12 | 2876 | 3468 | | | gvar | |
9 | q | 13 | 3468 | 3609 | | | gneg | |
9 | q | 21.11 | 3609 | 3792 | | | gpos | 25 |
9 | q | 21.12 | 3792 | 3876 | | | gneg | |
9 | q | 21.13 | 3876 | 4060 | | | gpos | 50 |
9 | q | 21.2 | 4060 | 4229 | | | gneg | |
9 | q | 21.31 | 4229 | 4440 | | | gpos | 50 |
9 | q | 21.32 | 4440 | 4638 | | | gneg | |
9 | q | 21.33 | 4638 | 4835 | | | gpos | 50 |
9 | q | 22.1 | 4835 | 5074 | | | gneg | |
9 | q | 22.2 | 5074 | 5173 | | | gpos | 25 |
9 | q | 22.31 | 5173 | 5314 | | | gneg | |
9 | q | 22.32 | 5314 | 5455 | | | gpos | 25 |
9 | q | 22.33 | 5455 | 5638 | | | gneg | |
9 | q | 31.1 | 5638 | 5892 | | | gpos | 100 |
9 | q | 31.2 | 5892 | 6005 | | | gneg | |
9 | q | 31.3 | 6005 | 6146 | | | gpos | 25 |
9 | q | 32 | 6146 | 6456 | | | gneg | |
9 | q | 33.1 | 6456 | 6681 | | | gpos | 75 |
9 | q | 33.2 | 6681 | 6822 | | | gneg | |
9 | q | 33.3 | 6822 | 6949 | | | gpos | 25 |
9 | q | 34.11 | 6949 | 7217 | | | gneg | |
9 | q | 34.12 | 7217 | 7302 | | | gpos | 25 |
9 | q | 34.13 | 7302 | 7443 | | | gneg | |
9 | q | 34.2 | 7443 | 7555 | | | gpos | 25 |
9 | q | 34.3 | 7555 | 7950 | | | gneg | | |
References
- Gilbert F, Kauff N . Disease genes and chromosomes: disease maps of the human genome. Chromosome 9 . Genet Test . 2001 . 157–74 . 5 . 2 . 11551106 . 10.1089/109065701753145664.
- Humphray SJ . DNA sequence and analysis of human chromosome 9 . Nature . 2004 . 369–74 . 429 . 6990 . 15164053 . 10.1038/nature02465 . 2734081 . vanc. Oliver K . Hunt AR . 3 . Plumb . R. W. . Loveland . J. E. . Howe . K. L. . Andrews . T. D. . Searle . S. . Hunt . S. E.. 2004Natur.429..369H .
- Wicking C, Berkman J, Wainwright B . Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome. Chromosome 9 . Genomics . 1994 . 505–11 . 22 . 3 . 8001963 . 10.1006/geno.1994.1423.
- Mäkelä-Bengs P, Järvinen N, Vuopala K, Suomalainen A, Palotie A, Peltonen L . The assignment the lethal congenital contracture syndrome (LCCS) locus to chromosome 9q33-34 . Am. J. Hum. Genet. . 61 . suppl . A30 . 1997 .
External links
- Web site: National Institutes of Health . Chromosome 9 . Genetics Home Reference . 2017-05-06 . 2007-06-30 . https://web.archive.org/web/20070630182713/http://ghr.nlm.nih.gov/chromosome=9 . dead .
- Web site: Chromosome 9. Human Genome Project Information Archive 1990–2003. 2017-05-06.
Notes and References
- Book: Tom Strachan. Andrew Read. Human Molecular Genetics. 2 April 2010. Garland Science. 978-1-136-84407-2. 45.
- 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. Between a chicken and a grape: estimating the number of human genes. . Genome Biol . 2010 . 11 . 5 . 206 . 20441615 . 10.1186/gb-2010-11-5-206 . 2898077 . free .
- Web site: Search results - 1[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene . NCBI . CCDS Release 20 for Homo sapiens . 2016-09-08 . 2017-05-28.
- Web site: Statistics & Downloads for chromosome 9 . HUGO Gene Nomenclature Committee . 2017-05-12 . 2017-05-19 . 2021-03-20 . https://web.archive.org/web/20210320210745/https://www.genenames.org/download/statistics-and-files/?c=9 . dead .
- Web site: Chromosome 9: Chromosome summary - Homo sapiens . Ensembl Release 88 . 2017-03-29 . 2017-05-19.
- Web site: Human chromosome 9: entries, gene names and cross-references to MIM . UniProt . 2018-02-28 . 2018-03-16.
- Web site: Search results - 9[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene . NCBI . 2017-05-19 . 2017-05-20.
- Web site: Search results - 9[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 . 2017-05-20.
- Web site: Search results - 9[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene . NCBI . 2017-05-19 . 2017-05-20.
- 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.
- 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.