Chromosome 19

Chromosome 19
Chromosome 19
	Human chromosome 19 pair after G-banding.; One is from mother, one is from father.
	Chromosome 19 pair; in human male karyogram.
Features
Length (bp)	61,707,364 bp; (CHM13)
No. of genes	1,357 (CCDS)
Type	Autosome
Centromere position	Metacentric; (26.2 Mbp)
Complete gene lists
CCDS	Gene list
HGNC	Gene list
UniProt	Gene list
NCBI	Gene list
External map viewers
Ensembl	Chromosome 19
Entrez	Chromosome 19
NCBI	Chromosome 19
UCSC	Chromosome 19
Full DNA sequences
RefSeq	NC_000019 (FASTA)
GenBank	CM000681 (FASTA)

Chromosome 19 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 19 spans more than 61.7 million base pairs, the building material of DNA. It is considered the most gene-rich chromosome containing roughly 1,500 genes, despite accounting for only 2 percent of the human genome.^[4]^[5]

Quick Facts Features, Length (bp) ...

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Number of genes

The following are some of the gene count estimates of human chromosome 19. 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.^[6]

More information Estimated by, Protein-coding genes ...

Estimated by	Protein-coding genes	Non-coding RNA genes	Pseudogenes	Source	Release date
CCDS	1,357	—	—	^[1]	2016-09-08
HGNC	1,372	299	413	^[7]	2017-05-12
Ensembl	1,469	894	514	^[8]	2017-03-29
UniProt	1,435	—	—	^[9]	2018-02-28
NCBI	1,430	604	528	^[10]^[11]^[12]	2017-05-19

Close

Gene list

The following is a partial list of genes on human chromosome 19. For complete list, see the link in the infobox on the right.

A1BG: encoding protein Alpha-1-B glycoprotein
AAVS1, viral integration site
ACSBG2: encoding enzyme Long-chain-fatty-acid—CoA ligase
ANKRD24: encoding protein Ankyrin repeat domain-containing protein 24
ARMC6: encoding protein Armadillo repeat-containing protein 6
ATG4D: encoding protein Autophagy related 4D, cysteine peptidase
ATP5SL: encoding protein ATP synthase subunit s-like protein
ATPase ASNA1: encoding enzyme ATPase ASNA1 also known as arsenical pump-driving ATPase and arsenite-stimulated ATPase
BTBD14B: encoding protein Nucleus accumbens-associated protein 1
C19orf18: encoding protein Chromosome 19 open reading frame 18
C19orf44: encoding protein Chromosome 19 open reading frame 44
C19orf70: encoding protein Chromosome 19 open reading frame 70
CACTIN: encoding protein Cactin
CCDC130: encoding protein Coiled-coil domain containing 130
CCDC151: encoding protein Coiled-coil domain containing 151
CCDC8: encoding protein Coiled-coil domain containing 8
CCDC94: encoding protein Coiled-coil domain containing 94 (CCDC94),
CXB3S: encoding protein Coxsackie virus B3 sensitivity
DHX34: encoding protein Dexh-box helicase 34
DNASE2: encoding protein Deoxyribonuclease II, lysosomal
DPF1: encoding protein D4, zinc and double PHD fingers family 1
EID2:
ETV2: encoding protein Ets variant 2
FIZ1: encoding protein FLT3 interacting zinc finger 1
HCST: encoding protein Hematopoietic cell signal transducer
HRC: encoding protein Sarcoplasmic reticulum histidine-rich calcium-binding protein
IFI30: encoding enzyme Gamma-interferon-inducible lysosomal thiol reductase
IGFL3: encoding protein IGF like family member 3
KRTDAP: encoding protein Keratinocyte differentiation-associated protein
LENG9: encoding protein Leukocyte Receptor Cluster Member 9 (LENG 9)
LIM2: encoding protein Lens fiber membrane intrinsic protein
LRG1: encoding protein Leucine-rich alpha-2-glycoprotein 1
LRRC25: encoding protein Leucine rich repeat containing 25
LSM4: encoding protein U6 snRNA-associated Sm-like protein LSm4
LSR: encoding protein Lipolysis-stimulated lipoprotein receptor
LYPD5: encoding protein LY6/PLAUR domain containing 5
MBOAT7: encoding enzyme Lysophospholipid acyltransferase 7
MOBKL2A: encoding enzyme Mps one binder kinase activator-like 2A
MZF1-AS1: encoding protein MZF1 antisense RNA 1
NCLN: encoding protein Nicalin
NFKBID: encoding protein Nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor
NOSIP: encoding enzyme Nitric oxide synthase-interacting protein
NWD1: NACHT and WD repeat domain containing 1.
OLFM2: encoding protein Olfactomedin 2
OSCAR: encoding protein Osteoclast-associated immunoglobulin-like receptor
PALM: encoding protein Paralemmin
PDCD5: encoding protein Programmed cell death protein 5
PEX11G: peroxisomal biogenesis factor 11 gamma
PGK1P2: encoding Phosphoglycerate kinase 1, pseudogene 2 protein
PLIN4: encoding protein Perilipin 4
PLVAP: encoding protein Plasmalemma vesicle-associated protein
PRR12: encoding protein Proline-rich 12
PRR36 (Proline Rich Region 36) encoding protein PRP36 (Proline Rich Protein 36)
KLK3: The Prostate-specific antigen (PSA)
PRX: Periaxin
PTOV1: encoding protein Prostate tumor overexpressed gene 1 protein
RFPL4A: encoding protein Ret finger protein like 4a
SBNO2: encoding protein Strawberry notch homolog 2 (Drosophila)
SEPW1: encoding protein Selenoprotein W
SFRS14: encoding protein Putative splicing factor, arginine/serine-rich 14
SFRS16: encoding protein Splicing factor, arginine/serine-rich 16
SLC5A5: Solute carrier family 5 (sodium iodide symporter), member 5
STK11: Serine/threonine kinase 11 (Peutz-Jeghers syndrome)
TBCB: encoding protein Tubulin-folding cofactor B
TECR: encoding enzyme Trans-2,3-enoyl-CoA reductase
THOP1: encoding enzyme Thimet oligopeptidase
TIMM50: encoding enzyme Mitochondrial import inner membrane translocase subunit TIM50
TIP39: encoding protein Tuberoinfundibular peptide of 39 residues
TMED1: encoding protein Transmembrane emp24 domain-containing protein 1
TMEM160: encoding protein Transmembrane protein 160
TMEM205: encoding protein Transmembrane Protein 205
UBXN6: encoding protein UBX domain protein 6
UCA1: a long non-coding RNA Urothelial cancer associated 1
UPK1A: encoding protein Uroplakin-1a
USE1: encoding protein Uncharacterized hematopoietic stem/progenitor cells protein MDS032
ZFP82: encoding protein ZFP82 zinc finger protein
ZSCAN4: Zinc finger and scan domain containing 4
ZSCAN18: encoding protein Zinc finger and SCAN domain containing 18
ZNF112: encoding protein Zinc finger protein 112
ZNF134: encoding protein Zinc finger protein 134
ZNF160: encoding protein Zinc finger protein 160
ZNF180: encoding protein Zinc finger protein 180
ZNF208: encoding protein Zinc finger protein 208
ZNF224: encoding protein Zinc finger protein 224
ZNF225: encoding protein Zinc finger protein 225
ZNF226: encoding protein Zinc finger protein 226
ZNF229: encoding protein Zinc finger protein 229
ZNF257: encoding protein Zinc finger protein 257
ZNF264: encoding protein Zinc finger protein 264
ZNF266: encoding protein Zinc finger protein 266
ZNF274: encoding protein Zinc finger protein 274
ZNF320: encoding protein Zinc finger protein 320
ZNF331: encoding protein Zinc finger protein 331
ZNF347: encoding protein Zinc finger protein 347
ZNF426: encoding protein Zinc finger protein 426
ZNF444: encoding protein Zinc finger protein 444
ZNF665 encoding protein Zinc finger protein 665
ZNF473: encoding protein Zinc finger protein 473
ZNF506: encoding protein Zinc finger protein 506
ZNF507: encoding protein Zinc finger protein 507
ZNF536: encoding protein Zinc finger protein 536
ZNF541: encoding protein Zinc finger protein 541
ZNF557: encoding protein Zinc finger protein 557
ZNF571: encoding protein Zinc finger protein 571
ZNF576: encoding protein Zinc finger protein 576
Zinc finger protein 613: encoding protein Zinc finger protein 613
ZNF649: Transcriptional suppressor
ZNF71: encoding protein Endothelial zinc finger protein induced by tumor necrosis factor alpha
ZNF737: encoding protein Zinc finger protein 737
ZNF749: encoding protein Zinc finger protein 749
ZNF676: encoding protein Zinc finger protein 676
ZNF772: encoding protein Zinc finger protein 772
ZNF784: encoding protein Zinc finger protein 784
ZNF8: encoding protein Zinc finger protein 8
ZNF83: encoding protein Zinc finger protein 83
ZNF878: encoding protein Zinc finger protein 878
ZNF880: encoding protein Zinc finger protein 880

Short arm

CACNA1A: Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit (Familial hemiplegic migraine Type I). Gene map locus 19p13
COMP: Cartilage oligomeric matrix protein. Gene map locus 19p13.1
NOTCH3: Notch homolog 3 (Drosophila): Gene map locus 19p13.1-p13.2
GCDH: Glutaryl-Coenzyme A dehydrogenase. Gene map locus 19p13.2
ZNF121: Zinc finger protein 121. Gene map locus 19p13.2
BSG: Basigin (Ok blood group)/Extracellular matrix metalloproteinase inducer/CD147. Gene map locus 19p13.3
ICAM4: Landsteiner and Weiner glycoprotein. Gene map locus 19p13.3
NRTN: Neurturin, associated with Hirschsprung's disease: Gene locus map 19p13.3
GTPBP3: GTP binding protein 3 19p13.11
KLF2: Krüppel-like factor 2, also known as Lung Krüppel-like factor. Gene map locus 19p13.11 OMIM: 602016
FAM32A: family with sequence similarity 32 member A 19q13.11
DDX39: DExD-box helicase 39. Gene map locus 19p13.12

Long arm

GAPDHS: glyceraldehyde-3-phosphate dehydrogenase, spermatogenic 19q13.12
HAMP: Hepcidin antimicrobial peptide. Gene map locus 19q13.12
BCKDHA: Branched chain keto acid dehydrogenase E1, alpha polypeptide (maple syrup urine disease). Gene map location 19q13.1-q13.2
APOE: Apolipoprotein E, gene associated with Alzheimer's disease. Gene map locus 19q13.2
CIC: Capicua transcriptional repressor. Gene map locus 19q13.2
FCGBP: Fc fragment of IgG binding protein
SARS2: seryl-tRNA synthetase 2, mitochondrial. Gene map locus 19q13.2
ATP1A3: ATPase. Gene map locus 19q13.31
DMWD: DM1 locus, WD repeat containing. Gene map locus 19q13.32
PNMA8A: paraneoplastic Ma antigen family member 8A 19q13.32
DMPK: Dystrophia myotonica-protein kinase. Gene map locus 19q13.32
GLTSCR2: Glioma tumor suppressor candidate region gene 2 protein 19q13.33
A1BG: Plasma glycoprotein, unknown function. Gene map locus 19q13.43
LRC: The Leukocyte Receptor Complex is a family of immunoreceptors expressed predominantly on monocytes and B cells and at lower levels on dendritic cells and natural killer (NK) cells. The LRC also includes the KIR locus. Gene map locus 19q13.4 OMIM: 604812
KPTN: Kaptin (actin binding protein) at the tips of stereocilia. Gene map locus 19q13.4^[13]
FUT1: The H locus is located on chromosome 19 at 19q13.3. It contains three exons that span more than 5 kb of genomic DNA, and it encodes a fucosyltransferase that produces the H antigen on RBCs.^[14]
FUT2: The Se locus is located on chromosome 19 at 19q13.3. It contains two exons that span about 25 kb of genomic DNA. The Se locus encodes a specific fucosyltransferase that is expressed in the epithelia of secretory tissues, such as salivary glands, the gastrointestinal tract, and the respiratory tract. The enzyme it encodes catalyzes the production of H antigen.^[14]
MORT (Mortal Obligate RNA Transcript, lincRNA): Gene map locus 19q13.43

The following diseases are some of those related to genes on chromosome 19:^[15]

G-banding ideograms of human chromosome 19

G-banding ideogram of human chromosome 19 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).

G-banding patterns of human chromosome 19 in three different resolutions (400,^[18] 550^[19] and 850^[3]). Band length in this diagram is based on the ideograms from ISCN (2013).^[20] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process.^[21]

More information Chr., Arm ...

G-bands of human chromosome 19 in resolution 850 bphs^[22]
Chr.	Arm^[23]	Band^[24]	ISCN start^[25]	ISCN stop^[25]	Basepair start	Basepair stop	Stain^[26]	Density
19	p	13.3	0	578	1	6,900,000	gneg
19	p	13.2	578	870	6,900,001	12,600,000	gpos	25
19	p	13.13	870	1034	12,600,001	13,800,000	gneg
19	p	13.12	1034	1216	13,800,001	16,100,000	gpos	25
19	p	13.11	1216	1581	16,100,001	19,900,000	gneg
19	p	12	1581	1809	19,900,001	24,200,000	gvar
19	p	11	1809	1992	24,200,001	26,200,000	acen
19	q	11	1992	2159	26,200,001	28,100,000	acen
19	q	12	2159	2372	28,100,001	31,900,000	gvar
19	q	13.11	2372	2569	31,900,001	35,100,000	gneg
19	q	13.12	2569	2737	35,100,001	37,800,000	gpos	25
19	q	13.13	2737	2949	37,800,001	38,200,000	gneg
19	q	13.2	2949	3101	38,200,001	42,900,000	gpos	25
19	q	13.31	3101	3193	42,900,001	44,700,000	gneg
19	q	13.32	3193	3390	44,700,001	47,500,000	gpos	25
19	q	13.33	3390	3649	47,500,001	50,900,000	gneg
19	q	13.41	3649	3770	50,900,001	53,100,000	gpos	25
19	q	13.42	3770	3938	53,100,001	55,800,000	gneg
19	q	13.43	3938	4120	55,800,001	58,617,616	gpos	25

Close

[1]
"Search results - 19[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.
[2]
Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
[3]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
[4]
Ucciferri, Charles (2004-03-31). "Gene-Rich Human Chromosome 19 Sequence Completed". DOE Joint Genome Institute. Retrieved 2022-12-10.
[5]
Sehgal, N.; Fritz, A. J.; Morris, K.; Torres, I.; Chen, Z.; Xu, J.; Berezney, R. (2014). "Gene Density and Chromosome Territory Shape". Chromosoma. 123 (5): 499–513. doi:10.1007/s00412-014-0480-y. PMC 5726871. PMID 25106753.
[6]
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.
[7]
"Statistics & Downloads for chromosome 19". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.
[8]
"Chromosome 19: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19.
[9]
"Human chromosome 19: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.
[10]
"Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
[11]
"Search results - 19[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.
[12]
"Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
[13]
Bearer EL, Chen AF, Chen AH, Li Z, Mark HF, Smith RJ, Jackson CL (2000). "2E4/Kaptin (KPTN)—a candidate gene for the hearing loss locus, DFNA4". Ann Hum Genet. 64 (3): 189–196. doi:10.1046/j.1469-1809.2000.6430189.x. PMC 3376086. PMID 11409409.
[14]
Dean, L. (2005). "Ch. 5: The ABO blood group". Blood Groups and Red Cell Antigens. Bethesda MD: National Center for Biotechnology Information. NBK2261.
[15]
Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 19". Genet Test. 1 (2): 145–9. doi:10.1089/gte.1997.1.145. PMID 10464639.
[16]
"OMIM Entry - # 613845 - HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME; HUPRAS". www.omim.org. Retrieved 20 January 2017.
[17]
Moss, K (Spring 2001). "Leber's Congenital Amaurosis". Texas Deafblind Outreach. Texas School for the Blind and Visually Impaired. Archived from the original on November 19, 2013.
[18]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
[19]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
[20]
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.
[21]
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. S2CID 16666470.
[22]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
[23]
"p": Short arm; "q": Long arm.
[24]
For cytogenetic banding nomenclature, see article locus.
[25]
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.
[26]
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.

Grimwood J, Gordon LA, Olsen A, Terry A, Schmutz J, Lamerdin J, Hellsten U, Goodstein D, Couronne O, Tran-Gyamfi M, Aerts A, Altherr M, Ashworth L, Bajorek E, Black S, Branscomb E, Caenepeel S, Carrano A, Caoile C, Chan YM, Christensen M, Cleland CA, Copeland A, Dalin E, Dehal P, Denys M, Detter JC, Escobar J, Flowers D, Fotopulos D, Garcia C, Georgescu AM, Glavina T, Gomez M, Gonzales E, Groza M, Hammon N, Hawkins T, Haydu L, Ho I, Huang W, Israni S, Jett J, Kadner K, Kimball H, Kobayashi A, Larionov V, Leem SH, Lopez F, Lou Y, Lowry S, Malfatti S, Martinez D, McCready P, Medina C, Morgan J, Nelson K, Nolan M, Ovcharenko I, Pitluck S, Pollard M, Popkie AP, Predki P, Quan G, Ramirez L, Rash S, Retterer J, Rodriguez A, Rogers S, Salamov A, Salazar A, She X, Smith D, Slezak T, Solovyev V, Thayer N, Tice H, Tsai M, Ustaszewska A, Vo N, Wagner M, Wheeler J, Wu K, Xie G, Yang J, Dubchak I, Furey TS, DeJong P, Dickson M, Gordon D, Eichler EE, Pennacchio LA, Richardson P, Stubbs L, Rokhsar DS, Myers RM, Rubin EM, Lucas SM (2004). "The DNA sequence and biology of human chromosome 19". Nature. 428 (6982): 529–35. Bibcode:2004Natur.428..529G. doi:10.1038/nature02399. PMID 15057824.
Human Proteome Project Launch website~ https://web.archive.org/web/20110726163128/http://www.hupo.org/research/hpp/HPP_legrain_sep_2010.pdf

National Institutes of Health. "Chromosome 19". Genetics Home Reference. Archived from the original on August 3, 2004. Retrieved 2017-05-06.
"Chromosome 19". Human Genome Project Information Archive 1990–2003. Retrieved 2017-05-06.

[CCDS-1] [1]
"Search results - 19[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.

[StrachanRead2010-2] [2]
Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.

[850bphs-3] [3]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.

[4] [4]
Ucciferri, Charles (2004-03-31). "Gene-Rich Human Chromosome 19 Sequence Completed". DOE Joint Genome Institute. Retrieved 2022-12-10.

[5] [5]
Sehgal, N.; Fritz, A. J.; Morris, K.; Torres, I.; Chen, Z.; Xu, J.; Berezney, R. (2014). "Gene Density and Chromosome Territory Shape". Chromosoma. 123 (5): 499–513. doi:10.1007/s00412-014-0480-y. PMC 5726871. PMID 25106753.

[pmid20441615-6] [6]
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.

[HGNC20170512-7] [7]
"Statistics & Downloads for chromosome 19". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.

[Ensembl_Release_88-8] [8]
"Chromosome 19: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19.

[UniProt-9] [9]
"Human chromosome 19: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.

[NCBI_coding-10] [10]
"Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.

[NCBI_noncoding-11] [11]
"Search results - 19[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.

[NCBI_pseudo-12] [12]
"Search results - 19[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.

[13] [13]
Bearer EL, Chen AF, Chen AH, Li Z, Mark HF, Smith RJ, Jackson CL (2000). "2E4/Kaptin (KPTN)—a candidate gene for the hearing loss locus, DFNA4". Ann Hum Genet. 64 (3): 189–196. doi:10.1046/j.1469-1809.2000.6430189.x. PMC 3376086. PMID 11409409.

[Dean05-14] [14]
Dean, L. (2005). "Ch. 5: The ABO blood group". Blood Groups and Red Cell Antigens. Bethesda MD: National Center for Biotechnology Information. NBK2261.

[15] [15]
Gilbert F (1997). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 19". Genet Test. 1 (2): 145–9. doi:10.1089/gte.1997.1.145. PMID 10464639.

[16] [16]
"OMIM Entry - # 613845 - HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME; HUPRAS". www.omim.org. Retrieved 20 January 2017.

[17] [17]
Moss, K (Spring 2001). "Leber's Congenital Amaurosis". Texas Deafblind Outreach. Texas School for the Blind and Visually Impaired. Archived from the original on November 19, 2013.

[400bphs-18] [18]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.

[550bphs-19] [19]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.

[Nomenclature2013-20] [20]
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.

[SethakulvichaiManitpornsut2012-21] [21]
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. S2CID 16666470.

[22] [22]
Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.

[23] [23]
"p": Short arm; "q": Long arm.

[24] [24]
For cytogenetic banding nomenclature, see article locus.

[ISCN-25] [25]
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.

[26] [26]
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.

[4]

[5]

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[2]

[3]

[6]

[7]

[8]

[9]

[10]

[11]

[12]

[13]

[14]

[15]

[16]

[17]

[18]

[19]

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[21]

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[26]

Number of genes

Gene list

Short arm

Long arm

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Chromosome 19

Number of genes

Gene list

Short arm

Long arm

Wikiwand in your browser!

Genes

Diseases and disorders

Cytogenetic band

References

External links

Chromosome 19
Human chromosome 19 pair after G-banding. One is from mother, one is from father.
Chromosome 19 pair in human male karyogram.
Features
Length (bp)	61,707,364 bp (CHM13)
No. of genes	1,357 (CCDS)^[1]
Type	Autosome
Centromere position	Metacentric^[2] (26.2 Mbp^[3])
Complete gene lists
CCDS	Gene list
HGNC	Gene list
UniProt	Gene list
NCBI	Gene list
External map viewers
Ensembl	Chromosome 19
Entrez	Chromosome 19
NCBI	Chromosome 19
UCSC	Chromosome 19
Full DNA sequences
RefSeq	NC_000019 (FASTA)
GenBank	CM000681 (FASTA)