Chromosome 4

Chromosome 4 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 4 spans more than 186 million base pairs (the building material of DNA) and represents between 6 and 6.5 percent of the total DNA in cells.

Chromosome 4
Human chromosome 4 pair after G-banding. One is from mother, one is from father.
Chromosome 4 pair
in human male karyogram.
Features
Length (bp)190,214,555 bp
(GRCh38)[1]
No. of genes727 (CCDS)[2]
TypeAutosome
Centromere positionSubmetacentric[3]
(50.0 Mbp[4])
Complete gene lists
CCDSGene list
HGNCGene list
UniProtGene list
NCBIGene list
External map viewers
EnsemblChromosome 4
EntrezChromosome 4
NCBIChromosome 4
UCSCChromosome 4
Full DNA sequences
RefSeqNC_000004 (FASTA)
GenBankCM000666 (FASTA)

Genomics

The chromosome is ~191 megabases in length. In a 2012 paper, 775 protein-encoding genes were identified on this chromosome.[5] 211 (27.9%) of these coding sequences did not have any experimental evidence at the protein level, in 2012. 271 appear to be membrane proteins. 54 have been classified as cancer-associated proteins.

Genes

Number of genes

The following are some of the gene count estimates of human chromosome 4. 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]

Estimated by Protein-coding genes Non-coding RNA genes Pseudogenes Source Release date
CCDS727—— [2] 2016-09-08
HGNC731277633 [7] 2017-05-12
Ensembl746993727 [8] 2017-03-29
UniProt765—— [9] 2018-02-28
NCBI769934819 [10][11][12] 2017-05-19

Gene list

The following is a partial list of genes on human chromosome 4. For complete list, see the link in the infobox on the right.

  • AASDH: aminoadipate-semialdehyde dehydrogenase
  • ACVR1: activin-like kinase 2 (ALK-2)
  • ACOX3: encoding enzyme Peroxisomal acyl-coenzyme A oxidase 3
  • AGA: AGU syndrome (Finnish heritage disease) related gene
  • AGPAT9: encoding enzyme Glycerol-3-phosphate acyltransferase 3 a.k.a. 1-acylglycerol-3-phosphate O-acyltransferase 9
  • ANK2: ankyrin 2, neuronal
  • APBB2: encoding protein Amyloid beta A4 precursor protein-binding family B member 2
  • ART3: encoding enzyme Ecto-ADP-ribosyltransferase 3
  • ASAHL: encoding enzyme N-acylethanolamine-hydrolyzing acid amidase
  • FAM198B: encoding protein Protein ENED
  • ZGRF1: zinc-finger GRF-type containing 1
  • CCDC109B: Coiled-coil domain containing 109B
  • CLNK: encoding protein Cytokine dependent hematopoietic cell linker
  • Complement Factor I: Complement Factor I
  • CRMP1: Collapsin response mediator protein 1, a member of CRMP family
  • CSN2: Beta-casein
  • CXCL1: chemokine (C-X-C motif) ligand 1, scyb1
  • CXCL2: chemokine (C-X-C motif) ligand 2, scyb2
  • CXCL3: chemokine (C-X-C motif) ligand 3, scyb3
  • CXCL4: chemokine (C-X-C motif) ligand 4, Platelet factor-4, PF-4, scyb4
  • CXCL5: chemokine (C-X-C motif) ligand 5, scyb5
  • CXCL6: chemokine (C-X-C motif) ligand 6, scyb6
  • CXCL7: chemokine (C-X-C motif) ligand 7, PPBP, scyb7
  • CXCL8: chemokine (C-X-C motif) ligand 8, interleukin 8 (IL-8), scyb8
  • CXCL9: chemokine (C-X-C motif) ligand 9, scyb9
  • CXCL10: chemokine (C-X-C motif) ligand 10, scyb10
  • CXCL11: chemokine (C-X-C motif) ligand 11, scyb11
  • CXCL13: chemokine (C-X-C motif) ligand 13, scyb13
  • CYTL1: Cytokine-like 1
  • DCUN1D4: Defective in cullin neddylation 1 domain containing 4
  • DHX15: DEAH-box helicase 15
  • DKK2: Dickkopf-related protein 2
  • DMAC1: encoding protein Transmembrane protein 261
  • DUX4: Thought to be inactive but 2010 research shows a key role in FSHD[13]
  • ELMOD2: Elmo domain-containing 2
  • EMCN: Endomucin
  • EVC: Ellis–Van Creveld syndrome
  • EVC2: Ellis–Van Creveld syndrome 2 (limbin)
  • Factor XI: Mutations cause Haemophilia C
  • FAM47E-STBD1: FAM47E-STBD1 readthrough
  • FAM114A1: Family with sequence similarity 114, member A1
  • FAM149A: Family with sequence similarity 149, member A
  • FAM193A: Family with sequence similarity 193, member A
  • FAM221B: Family with sequence similarity 221, member B
  • FGF2: Fibroblast growth factor 2 (basic fibroblast growth factor)
  • FGFR3: fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism, bladder cancer)
  • FGFRL1: fibroblast growth factor receptor-like 1
  • FRG1: FSHD region gene 1
  • GUF1: GUF1 homolog, GTPase
  • HCL2: encoding hair color 2 (red) protein
  • HDL3: encoding Huntington-like neurodegenerative disorder 2 protein
  • HELQ: encoding protein Helicase, POLQ-like
  • HTT (Huntingtin): huntingtin protein (Huntington's disease)
  • IGJ: linker protein for immunoglobulin alpha and mu polypeptides
  • INTS12: Integrator complex subunit 12
  • KDR: Kinase insert domain receptor (Vascular endothelial growth factor receptor 2)
  • KIAA1530: UV stimulated scaffold protein A
  • LCORL: Ligand dependent nuclear receptor corepressor like
  • LDB2: LIM domain-binding protein 2
  • LGI2: Leucine-rich repeat LGI family member 2
  • LOC100505912 encoding protein Uncharacterized LOC100505912
  • LSM6: U6 snRNA-associated Sm-like protein
  • LYAR: Cell growth-regulating nucleolar protein
  • MAB21L2: Mab-21-like 2
  • Marcksl1: encoding protein MARCKS-like 1
  • MAML3: Mastermind-like 3
  • MFSD7: encoding protein Major facilitator superfamily domain containing 7
  • MIR1269A: microRNA 1269a
  • MIR95: non-coding RNA MicroRNA 95
  • MLF1IP: Centromere protein U
  • MMAA: methylmalonic aciduria (cobalamin deficiency) cblA type
  • MTHFD2L: NAD-dependent methylenetetrahydrofolate dehydrogenase 2-like protein
  • MYL5: Myosin light chain 5
  • NOA1: encoding protein Nitric oxide associated 1
  • NUDT6: nudix hydrolase 6
  • NUDT9: nudix hydrolase 9
  • OTUD4: OTU domain-containing protein 4
  • PABPC4L: encoding protein Poly(A) binding protein, cytoplasmic 4-like
  • PARM1: Prostate androgen-regulated mucin-like protein 1
  • PHOX2B: codes for a homeodomain transcription factor
  • PI4K2B: Phosphatidylinositol 4-kinase type 2-beta
  • PKD2: polycystic kidney disease 2 (autosomal dominant)
  • PLAC8: encoding protein Placenta specific 8
  • PLK4: Serine/threonine-protein kinase PLK4
  • PSAPL1: encoding protein Prosaposin-like 1 (gene/pseudogene)
  • QDPR: quinoid dihydropteridine reductase
  • RBM47: RNA binding motif protein 47
  • RG9MTD2: encoding protein RNA (guanine-9-) methyltransferase domain containing 2
  • SDAD1: protein SDA1 homolog
  • SEC24B: Sec24 homolog B
  • SEC24D: Sec24 homolog D
  • SEPT11: Septin-11
  • SLC9B2: solute carrier family 9 member B2
  • SLC10A4: solute carrier family 10 member 4
  • SMIM20: encoding protein Small integral membrane protein 20
  • SNCA: synuclein, alpha (non A4 component of amyloid precursor)
  • SPATA5: Spermatogenesis-associated protein 5
  • STATH: gene with protein product
  • TACC3: Transforming acidic coiled-coil-containing protein 3
  • TENM3: Teneurin transmembrane protein 3
  • THAP6: THAP domain-containing protein 6
  • TMEM155: encoding protein Transmembrane protein 155
  • TMEM165: encoding protein Transmembrane protein 165
  • TMEM243: encoding protein Transmembrane protein 243
  • TMPRSS11D: Transmembrane protease, serine 11D
  • TMPRSS11F: encoding protein Transmembrane serine protease 11F
  • TNIP2: TNFAIP3-interaction protein 2
  • UCHL1: ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
  • UGT8: UDP glycosyltransferase 8
  • UNC5C: netrin receptor UNC5C
  • UPF0602: encoding UPF0602 Protein C4orf47
  • USP38: encoding protein Ubiquitin specific peptidase 38
  • USP53: ubiquitin specific peptidase 53
  • UTP3: small subunit processome component
  • WFS1: Wolfram syndrome 1 (wolframin)
  • ZNF621: encoding protein Zinc finger protein 621

Diseases and disorders

The following are some of the diseases related to genes located on chromosome 4:

Cytogenetic band
G-banding ideograms of human chromosome 4
G-banding ideogram of human chromosome 4 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 4 in three different resolutions (400,[14] 550[15] and 850[4]). Band length in this diagram is based on the ideograms from ISCN (2013).[16] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process.[17]
G-bands of human chromosome 4 in resolution 850 bphs[18]
Chr. Arm[19] Band[20] ISCN
start[21]		 ISCN
stop[21]		 Basepair
start		 Basepair
stop		 Stain[22] Density
4p 16.3022014500000 gneg
4p 16.22203894,500,0016,000,000 gpos25
4p 16.13897796,000,00111,300,000 gneg
4p 15.33779106611,300,00115,000,000 gpos50
4p 15.321066128615,000,00117,700,000 gneg
4p 15.311286155717,700,00121,300,000 gpos75
4p 15.21557181121,300,00127,700,000 gneg
4p 15.11811216627,700,00135,800,000 gpos100
4p 142166250535,800,00141,200,000 gneg
4p 132505274241,200,00144,600,000 gpos50
4p 122742287744,600,00148,200,000 gneg
4p 112877304648,200,00150,000,000 acen
4q 113046324950,000,00151,800,000 acen
4q 123249357151,800,00158,500,000 gneg
4q 13.13571391058,500,00165,500,000 gpos100
4q 13.23910406265,500,00169,400,000 gneg
4q 13.34062433369,400,00175,300,000 gpos75
4q 21.14333450275,300,00178,000,000 gneg
4q 21.214502467178,000,00181,500,000 gpos50
4q 21.224671473981,500,00183,200,000 gneg
4q 21.234739487483,200,00186,000,000 gpos25
4q 21.34874514586,000,00187,100,000 gneg
4q 22.15145551787,100,00192,800,000 gpos75
4q 22.25517563692,800,00194,200,000 gneg
4q 22.35636589094,200,00197,900,000 gpos75
4q 235890605997,900,001100,100,000 gneg
4q 2460596347100,100,001106,700,000 gpos50
4q 2563476685106,700,001113,200,000 gneg
4q 2666857040113,200,001119,900,000 gpos75
4q 2770407277119,900,001122,800,000 gneg
4q 28.172777565122,800,001127,900,000 gpos50
4q 28.275657734127,900,001130,100,000 gneg
4q 28.377348259130,100,001138,500,000 gpos100
4q 31.182598581138,500,001140,600,000 gneg
4q 31.2185818733140,600,001145,900,000 gpos25
4q 31.2287338851145,900,001147,500,000 gneg
4q 31.2388519004147,500,001150,200,000 gpos25
4q 31.390049207150,200,001154,600,000 gneg
4q 32.192079545154,600,001160,800,000 gpos100
4q 32.295459681160,800,001163,600,000 gneg
4q 32.396819985163,600,001169,200,000 gpos100
4q 33998510087169,200,001171,000,000 gneg
4q 34.11008710341171,000,001175,400,000 gpos75
4q 34.21034110408175,400,001176,600,000 gneg
4q 34.31040810628176,600,001182,300,000 gpos100
4q 35.11062810967182,300,001186,200,000 gneg
4q 35.21096711170186,200,001190,214,555 gpos25

References
  1. "Human Genome Assembly GRCh38 - Genome Reference Consortium". National Center for Biotechnology Information. 2013-12-24. Retrieved 2017-03-04.
  2. "Search results - 4[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.
  3. Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
  4. Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
  5. Chen LC, Liu MY, Hsiao YC, Choong WK, Wu HY, Hsu WL, Liao PC, Sung TY, Tsai SF, Yu JS, Chen YJ (2012) Decoding the disease-associated proteins encoded in the human chromosome 4. J Proteome Res
  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 4". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.
  8. "Chromosome 4: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Retrieved 2017-05-19.
  9. "Human chromosome 4: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.
  10. "Search results - 4[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 - 4[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 - 4[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  13. Lemmers RJ, van der Vliet PJ, Klooster R, Sacconi S, Camaño P, Dauwerse JG, Snider L, Straasheijm KR, van Ommen GJ, Padberg GW, Miller DG, Tapscott SJ, Tawil R, Frants RR, van der Maarel SM (September 2010). "A unifying genetic model for facioscapulohumeral muscular dystrophy". Science. 329 (5999): 1650–3. Bibcode:2010Sci...329.1650L. doi:10.1126/science.1189044. PMC 4677822. PMID 20724583.
  14. Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
  15. Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
  16. 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.
  17. Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012). "Estimation of band level resolutions of human chromosome images". In Computer Science and Software Engineering (JCSSE), 2012 International Joint Conference on: 276–282. doi:10.1109/JCSSE.2012.6261965. ISBN 978-1-4673-1921-8. S2CID 16666470.
  18. Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
  19. "p": Short arm; "q": Long arm.
  20. For cytogenetic banding nomenclature, see article locus.
  21. 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.
  22. 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.

Further reading
  • Goldfrank D, Schoenberger E, Gilbert F (2003). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 4". Genet Test. 7 (4): 351–72. doi:10.1089/109065703322783752. PMID 15000816.
Wikimedia Commons has media related to Human chromosome 4.
  • National Institutes of Health. "Chromosome 4". Genetics Home Reference. Archived from the original on August 3, 2004. Retrieved 2017-05-06.
  • "Chromosome 4". Human Genome Project Information Archive 1990–2003. Retrieved 2017-05-06.
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