Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Genes  



1.1  Number of genes  





1.2  Gene list  







2 Diseases and disorders  





3 Cytogenetic band  





4 References  





5 External links  














Chromosome 12






العربية

 / Bân-lâm-gú
Bosanski
Català
Deutsch
Español
فارسی
Français
Galego
Hrvatski
Italiano
Latina
Magyar
Nederlands
Norsk bokmål
Polski
Português
Română
Русский
Српски / srpski
Srpskohrvatski / српскохрватски
Svenska
Tagalog
Türkçe
Українська
Tiếng Vit

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


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 genes988 (CCDS)[1]
TypeAutosome
Centromere positionSubmetacentric[2]
(35.5 Mbp[3])
Complete gene lists
CCDSGene list
HGNCGene list
UniProtGene list
NCBIGene list
External map viewers
EnsemblChromosome 12
EntrezChromosome 12
NCBIChromosome 12
UCSCChromosome 12
Full DNA sequences
RefSeqNC_000012 (FASTA)
GenBankCM000674 (FASTA)

Chromosome 12 is one of the 23 pairs of chromosomesinhumans. 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

[edit]

Number of genes

[edit]

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

[edit]

The following is a partial list of genes on human chromosome 12. For complete list, see the link in the infobox on the right.

  • ACAD10: encoding protein Acyl-CoA dehydrogenase family, member 10
  • ACSS3: encoding protein Acyl-CoA synthetase short-chain family member 3
  • ACVRL1: activin A receptor type II-like 1f
  • ANKRD33: encoding protein Ankyrin repeat domain 33
  • APOF: encoding protein Apolipoprotein F
  • APOLD1: apolipoprotein L domain containing 1
  • ARL6IP4: encoding protein ADP-ribosylation-like factor 6 interacting protein 4
  • ARPC3: encoding protein Actin-related protein 2/3 complex subunit 3
  • Asun: encoding protein Protein asunder homolog (Asun)
  • ATP2B1-AS1: encoding protein Atp2b1 antisense rna 1
  • ATG101: Autophagy-related protein 101
  • BCAT1: encoding protein Branched chain amino acid transaminase 1
  • C12orf24: encoding protein FAM216A
  • C12orf42: encoding protein uncharacterised chromosome 12 open reading frame 42
  • C12orf43: encoding protein. Uncharacterized.
  • C12orf60: encoding protein Uncharacterized protein C12orf60
  • CALCOCO1: Calcium-binding and coiled-coil domain-containing protein 1
  • CBX5: chromobox homolog 5
  • CCDC53: Coiled-coil domain-containing protein 53
  • CKAP4: Cytoskeleton associated protein 4
  • CNOT2: encoding protein CCR4-NOT transcription complex subunit 2
  • CNPY2: encoding protein Canopy FGF signaling regulator 2
  • CCDC42B: encoding protein Coiled Coil Domain Containing protein 42B
  • COL2A1: collagen, type II, alpha 1 (primary osteoarthritis, spondyloepiphyseal dysplasia, congenital)
  • CRACR2A: encoding protein Calcium release activated channel regulator 2A
  • CSRP2: Cysteine and glycine-rich protein 2
  • DDX23: DEAD-box helicase 23
  • DDX47: DEAD-box helicase 47
  • DHH: Desert hedgehog protein
  • DPPA3: Developmental pluripotency-associated protein 3
  • DPY19L2: encoding protein Dpy-19-like 2 (C. elegans)
  • E2F7: E2F transcription factor 7
  • EMP1: Epithelial membrane protein 1
  • ERGIC2: encoding protein a protein of 377 amino acid residues
  • FAM60A: encoding protein FAM60A
  • FAM186B: encoding protein Protein FAM186B
  • GABARAPL1: encoding protein Gaba type a receptor associated protein like 1
  • GPD1: encoding protein Glycerol-3-phosphate dehydrogenase 1
  • GOLT1B: Golgi transport 1B
  • GPN3: encoding enzyme GPN-loop GTPase 3
  • HNF1A-AS1: encoding protein HNF1A antisense RNA 1
  • HPD: 4-hydroxyphenylpyruvate dioxygenase
  • IFFO1: encoding protein Intermediate filament family orphan 1
  • KANSL2: encoding protein KAT8 regulatory NSL complex subunit 2 (KANSL2)
  • KCNA1: potassium voltage-gated channel subfamily A member 1 at 12p13.32
  • KDM2B: encoding protein Lysine (K)-specific demethylase 2B
  • KERA: keratocan
  • KRAS: V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog
  • LARP4: encoding protein La-related protein 4
  • LEPREL2: encoding enzyme Prolyl 3-hydroxylase 3
  • LMBR1L: encoding protein Protein LMBR1L
  • LRRC23: encoding protein Leucine-rich repeat-containing protein 23
  • LRRIQ1: encoding protein Leucine-rich repeats and IQ motif containing 1
  • LRRK2: leucine-rich repeat kinase 2
  • MBOAT5: encoding enzyme Lysophospholipid acyltransferase 5
  • METTL1: encoding enzyme tRNA (guanine-N(7)-)-methyltransferase
  • MFAP5: encoding protein Microfibrillar-associated protein 5
  • MIR196A2: encoding microRNA MicroRNA 196a-2
  • MMAB: methylmalonic aciduria (cobalamin deficiency) cblB type
  • MON2: encoding protein Protein MON2 homolog
  • MUCL1: encoding protein Mucin-like protein 1
  • MYO1A: myosin IA
  • NANOG: NK-2 type homeodomain gene
  • NAP1L1: encoding protein Nucleosome assembly protein 1-like 1
  • NRIP2: encoding protein Nuclear receptor-interacting protein 2
  • NUDT4: encoding enzyme Diphosphoinositol polyphosphate phosphohydrolase 2
  • PAH: phenylalanine hydroxylase
  • PIP4K2C: encoding protein Phosphatidylinositol-5-phosphate 4-kinase, type II, gamma
  • PIWIL1: encoding protein Piwi-like protein 1
  • PLBD1: encoding protein Phospholipase B domain containing 1 1
  • POP5: encoding enzyme Ribonuclease P/MRP protein subunit POP5
  • PPHLN1: encoding protein Periphilin-1
  • PPP1R12A: protein phosphatase 1, regulatory (inhibitor) subungfdit 12A
  • PRB1: encoding protein Basic salivary proline-rich protein 1
  • PRB3: encoding protein Basic salivary proline-rich protein 3
  • PRB4: encoding protein Basic salivary proline-rich protein 4
  • PRH1: encoding protein Salivary acidic proline-rich phosphoprotein 1/2
  • PRH2: encoding protein Proline-rich protein HaeIII subfamily 2
  • PRMT8: encoding protein Protein arginine methyltransferase 8
  • PRR4: encoding protein Proline-rich protein 4
  • PTMS: encoding protein Parathymosin
  • PTPN11: protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1)
  • PUS1: encoding enzyme tRNA pseudouridine synthase A
  • PUS7L: encoding enzyme Pseudouridylate synthase 7 homolog-like protein
  • PZP: encoding protein Pregnancy zone protein
  • RAB3IP: encoding protein RAB3A-interacting protein
  • RASSF8: encoding protein Ras association domain-containing protein 8
  • RASSF9: encoding protein Ras association domain-containing protein 9
  • RERG: encoding protein RAS-like, estrogen-regulated, growth inhibitor
  • RNF34: encoding enzyme E3 ubiquitin-protein ligase RNF34
  • SARNP: SAP domain-containing ribonucleoprotein
  • Serpina3f: encoding protein Serine (or cysteine) peptidase inhibitor, clade A, member 3F
  • SHMT2: encoding protein Serine hydroxymethyltransferase 2
  • SLC8B1: solute carrier family 8 member B1
  • TBC1D15: encoding protein TBC1 domain family member 15
  • TBX3: encoding protein T-box transcription factor3
  • TCHP: encoding protein Trichoplein keratin filament-binding protein
  • TESPA1: encoding protein Thymocyte expressed, positive selection associated 1
  • THAP2: encoding protein THAP domain-containing protein 2
  • TMTC1: encoding protein Transmembrane and tetratricopeptide repeat containing 1
  • TMEM117: encoding protein Transmembrane protein 117
  • TRAFD1: encoding protein TRAF-type zinc finger domain-containing protein 1
  • TSFM: encoding protein Elongation factor Ts, mitochondrial
  • TWF1: twinfilin-1
  • UNQ1887:
  • USP52: encoding enzyme PAB-dependent poly(A)-specific ribonuclease subunit 2
  • UTP20: encoding protein Small subunit processome component 20 homolog
  • VEZT: encoding protein Vezatin
  • YAF2: encoding protein YY1-associated factor 2
  • ZCCHC8: encoding protein Zinc finger CCHC domain-containing protein 8
  • ZFC3H1: encoding protein Zinc finger C3H1-type containing
  • ZNF26: encoding protein Zinc finger protein 26
  • ZNF84: encoding protein Zinc finger protein 84
  • ZNF268: encoding protein Zinc finger protein 268
  • ZNF664: encoding protein Zinc finger protein 664
  • Diseases and disorders

    [edit]

    The following diseases are some of those related to genes on chromosome 12:

  • bipolar disorder
  • 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
  • schizophrenia
  • 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

    [edit]
    G-banding ideograms of human chromosome 12
    G-banding ideogram of human chromosome 12 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 12 in three different resolutions (400,[12] 550[13] and 850[3]). Band length in this diagram is based on the ideograms from ISCN (2013).[14] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process.[15]
    G-bands of human chromosome 12 in resolution 850 bphs[3]
    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

    [edit]
    1. ^ a b "Search results - 12[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.
  • ^ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
  • ^ a b c 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. PMC 2898077. PMID 20441615.
  • ^ "Statistics & Downloads for chromosome 12". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.
  • ^ "Chromosome 12: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19.
  • ^ "Human chromosome 12: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.
  • ^ "Search results - 12[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  • ^ "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". NCBI. 2017-05-19. Retrieved 2017-05-20.
  • ^ "Search results - 12[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  • ^ 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. PMC 1199301. 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.
  • ^ 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.
  • ^ "p": Short arm; "q": Long arm.
  • ^ For cytogenetic banding nomenclature, see article locus.
  • ^ a b 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.
  • Montgomery KT, Lee E, Miller A, Lau S, Shim C, Decker J, Chiu D, Emerling S, Sekhon M, Kim R, Lenz J, Han J, Ioshikhes I, Renault B, Marondel I, Yoon SJ, Song K, Murty VV, Scherer S, Yonescu R, Kirsch IR, Ried T, McPherson J, Gibbs R, Kucherlapati R (2001). "A high-resolution map of human chromosome 12". Nature. 409 (6822): 945–6. Bibcode:2001Natur.409..945M. doi:10.1038/35057174. PMID 11237017.
  • [edit]
    Retrieved from "https://en.wikipedia.org/w/index.php?title=Chromosome_12&oldid=1216077193"

    Categories: 
    Chromosomes (human)
    Genes on human chromosome 12
    Hidden categories: 
    Articles with short description
    Short description is different from Wikidata
    Pages using multiple image with manual scaled images
    Commons category link is on Wikidata
    Articles with J9U identifiers
    Articles with LCCN identifiers
     



    This page was last edited on 28 March 2024, at 22:13 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki