Open Access Articles- Top Results for Chromosome 5 (human)

Chromosome 5 (human)

Chromosome 5 (human)
Length (bp) 181,538,259 bp
Number of genes 1,892
Type Autosome
Centromere position Submetacentric [1]
RefSeq NC_000005
GenBank CM000667

Chromosome 5 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 5 spans about 181 million base pairs (the building blocks of DNA) and represents almost 6% of the total DNA in cells. Chromosome 5 is the 5th largest human chromosomes, yet has one of the lowest gene densities. This is partially explained by numerous gene-poor regions that display a remarkable degree of non-coding and syntenic conservation with non-mammalian vertebrates, suggesting they are functionally constrained.[2]

Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 5 likely contains between 900 and 1,300 genes.

Because chromosome 5 is responsible for many forms of growth and development (cell divisions) changes may cause cancers. One example would be acute myeloid leukemia (AML). [3]


The following are some of the genes located on chromosome 5:

  • ADAMTS2: ADAM metallopeptidase with thrombospondin type 1 motif, 2
  • APC: adenomatosis polyposis coli
  • CAST: Calpastatin
  • EGR1: early growth response protein 1
  • ERAP1: endoplasmic reticulum aminopeptidase 1 (previously called ARTS-1)
  • ERAP2: endoplasmic reticulum aminopeptidase 2
  • DTDST: diastrophic dysplasia sulfate transporter
  • ERCC8: excision repair cross-complementing rodent repair deficiency, complementation group 8
  • FGFR4: fibroblast growth factor receptor 4
  • GM2A: GM2 ganglioside activator
  • HEXB: hexosaminidase B (beta polypeptide)
  • IRX1: Iroquois-class homeodomain protein (human)
  • MASS1: monogenic, audiogenic seizure susceptibility 1 homolog (mouse)
  • MCCC2: methylcrotonoyl-Coenzyme A carboxylase 2 (beta)
  • MEF2C: Myocyte-specific enhancer factor 2C
  • MTRR: 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
  • NIPBL: Nipped-B homolog (Drosophila)
  • NSD1: Transcription coregulator protein
  • Pikachurin: Responsible for the functioning of the ribbon synapses; allows the eye to track moving objects
  • SLC22A5: solute carrier family 22 (organic cation transporter), member 5
  • SLC26A2: solute carrier family 26 (sulfate transporter), member 2
  • SH3TC2: domain and tetratricopeptide repeats 2
  • SMN1: survival motor neuron 1, telomeric
  • SMN2: survival motor neuron 2, centromeric
  • SNCAIP: synuclein, alpha interacting protein (synphilin)
  • SPINK5: serine protease inhibitor Kazal-type 5 (LEKTI)
  • SPINK6: serine protease inhibitor Kazal-type 6
  • SPINK9: serine protease inhibitor Kazal-type 9 (LEKTI-2)
  • TCOF1: Treacher Collins-Franceschetti syndrome 1
  • TGFBI: keratoepithelin
  • TTC37: Tetratricopeptide repeat domain 37
  • FGF1: fibroblast growth factor 1 (acidic fibroblast growth factor)

Diseases & disorders

The following are some of the diseases related to genes located on chromosome 5:

Chromosomal conditions

The following conditions are caused by changes in the structure or number of copies of chromosome 5:

  • Cri-du-chat syndrome is caused by a deletion of the end of the short (p) arm of chromosome 5. This chromosomal change is written as 5p-. The signs and symptoms of cri-du-chat syndrome are probably related to the loss of multiple genes in this region. Researchers have not identified all of these genes or determined how their loss leads to the features of the disorder. They have discovered, however, that a larger deletion tends to result in more severe mental retardation and developmental delays in people with cri-du-chat syndrome.[4][5][6]
Researchers have defined narrow regions of the short arm of chromosome 5 that are associated with particular features of cri-du-chat syndrome. A specific region designated 5p15.3 is associated with a cat-like cry, and a nearby region called 5p15.2 is associated with mental retardation, small head (microcephaly), and distinctive facial features.
  • Familial Adenomatous Polyposis is caused by a deletion of the APC tumor suppressor gene on the long (q) arm of chromosome 5. This chromosomal change results in thousands of colonic polyps which gives the patient a 100% risk of colon cancer if total colectomy is not done.
  • Other changes in the number or structure of chromosome 5 can have a variety of effects, including delayed growth and development, distinctive facial features, birth defects, and other medical problems. Changes to chromosome 5 include an extra segment of the short (p) or long (q) arm of the chromosome in each cell (partial trisomy 5p or 5q), a missing segment of the long arm of the chromosome in each cell (partial monosomy 5q), and a circular structure called ring chromosome 5. A ring chromosome occurs when both ends of a broken chromosome are reunited.


  1. ^ "Table 2.3: Human chromosome groups". Human Molecular Genetics (2nd ed.). Garland Science. 1999. 
  2. ^ Home - Homo sapiens
  3. ^ "Chromosome 5". Genetics Home Reference. Lister Hill National Center for Biomedical Communications. U.S. National Library of Medicine. December 2014. 
  4. ^ Cornish K, Bramble D; Bramble (2002). "Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management". Dev Med Child Neurol 44 (7): 494–7. PMID 12162388. doi:10.1017/S0012162201002419. 
  5. ^ Wu Q, Niebuhr E, Yang H, Hansen L; Niebuhr; Yang; Hansen (2005). "Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR". Eur J Hum Genet 13 (4): 475–85. PMID 15657623. doi:10.1038/sj.ejhg.5201345. 
  6. ^ Zhang X, Snijders A, Segraves R, Zhang X, Niebuhr A, Albertson D, Yang H, Gray J, Niebuhr E, Bolund L, Pinkel D; Snijders; Segraves; Zhang; Niebuhr; Albertson; Yang; Gray; Niebuhr; Bolund; Pinkel (2005). "High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization". Am J Hum Genet 76 (2): 312–26. PMC 1196376. PMID 15635506. doi:10.1086/427762.