Chromosome 5 (human)
|Chromosome 5 (human)|
Human chromosome 5 pair after G-banding.
One is from mother, one is from father.
Chromosome 5 pair in human male karyogram.
|Length (bp)||181,538,259 bp|
|Number of genes||1,892|
|Centromere position||Submetacentric |
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.
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.
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:
- Achondrogenesis type 1B
- Atelosteogenesis, type II
- Charcot–Marie–Tooth disease, type 4
- Cockayne syndrome
- Cornelia de Lange syndrome
- Corneal dystrophy of Bowman layer, type I
- Corneal dystrophy of Bowman layer, type II
- Cri du Chat
- Diastrophic dysplasia
- Ehlers-Danlos syndrome
- Ehlers-Danlos syndrome, dermatosparaxis type
- Familial adenomatous polyposis
- Granular corneal dystrophy type I
- Granular corneal dystrophy type II
- GM2-gangliosidosis, AB variant
- 3-Methylcrotonyl-CoA carboxylase deficiency
- Myelodysplastic Syndrome
- Netherton syndrome
- Nicotine dependency
- Nipple Disease
- Parkinson's disease
- Primary carnitine deficiency
- Recessive multiple epiphyseal dysplasia
- Sandhoff disease
- Spinal muscular atrophy
- Sotos Syndrome
- Survival motor neuron spinal muscular atrophy
- Treacher Collins syndrome
- Tricho-hepato-enteric syndrome
- Usher syndrome
- Usher syndrome type II
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.
- 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.
- Chromosome 5q deletion syndrome is caused by the deletion of the q arm (long arm) of chromosome 5. This deletion has been linked to several blood related disorders including Myelodysplastic syndrome and Erythroblastopenia[disambiguation needed]. This is a different condition than Cri-du-chat which was mentioned above.
- 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.
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- Home - Homo sapiens
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