Chromosome 13 (human)

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Chromosome 13 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 13 spans about 113 million base pairs (the building material of DNA) and represents between 3.5 and 4 % of the total DNA in cells.

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 13 likely contains between 300 and 700 genes.

1 Genes
2 Diseases & disorders
3 Chromosomal conditions
4 References

[edit] Genes

The following are some of the genes located on chromosome 13:

ATP7B: ATPase, Cu++ transporting, beta polypeptide (Wilson disease)
BRCA2: breast cancer 2, early onset
EDNRB: endothelin receptor type B
GJB2: gap junction protein, beta 2, 26kDa (connexin 26)
GJB6: gap junction protein, beta 6 (connexin 30)
PCCA: propionyl Coenzyme A carboxylase, alpha polypeptide
RB1: retinoblastoma 1 (including osteosarcoma)
FLT1: Fms related tyrosine kinase 1 (Vascular endothelial growth factor receptor 1)

[edit] Diseases & disorders

The following diseases are some of those related to genes on chromosome 13:

Bladder cancer
Breast cancer
Maturity onset diabetes of the young type 4
Nonsyndromic deafness
Nonsyndromic deafness, autosomal dominant
Nonsyndromic deafness, autosomal recessive
Propionic acidemia
Retinoblastoma
Waardenburg syndrome
Wilson disease

[edit] Chromosomal conditions

The following conditions are caused by changes in the structure or number of copies of chromosome 13:

Retinoblastoma: A small percentage of retinoblastoma cases are caused by deletions in the region of chromosome 13 (13q14) containing the RB1 gene. Children with these chromosomal deletions may also have mental retardation, slow growth, and characteristic facial features (such as prominent eyebrows, a broad nasal bridge, a short nose, and ear abnormalities). Researchers have not determined which other genes are located in the deleted region, but a loss of several genes is likely responsible for these developmental problems.
Trisomy 13: Trisomy 13 occurs when each cell in the body has three copies of chromosome 13 instead of the usual two copies. Trisomy 13 can also result from an extra copy of chromosome 13 in only some of the body's cells (mosaic trisomy 13). In a small percentage of cases, trisomy 13 is caused by a rearrangement of chromosomal material between chromosome 13 and another chromosome. As a result, a person has the two usual copies of chromosome 13, plus extra material from chromosome 13 attached to another chromosome. These cases are called translocation trisomy 13. Extra material from chromosome 13 disrupts the course of normal development, causing the characteristic signs and symptoms of trisomy 13. Researchers are not yet certain how this extra genetic material leads to the features of the disorder.
Other chromosomal conditions: Partial monosomy 13q is a rare chromosomal disorder that results when a piece of the long arm (q) of chromosome 13 is missing (monosomic). Infants born with partial monosomy 13q may exhibit low birth weight, malformations of the head and face (craniofacial region), skeletal abnormalities (especially of the hands and feet), and other physical abnormalities. Mental retardation is characteristic of this condition. The mortality rate during infancy is high among individuals born with this disorder. Almost all cases of partial monosomy 13q occur randomly for no apparent reason (sporadic).

[edit] References

Baud O, Cormier-Daire V, Lyonnet S, Desjardins L, Turleau C, Doz F (1999). "Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion". Clin Genet 55 (6): 478-82. PMID 10450867.
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Gilbert F (2000). "Chromosome 13". Genet Test 4 (1): 85-94. PMID 10794368.
Kivela T, Tuppurainen K, Riikonen P, Vapalahti M (2003). "Retinoblastoma associated with chromosomal 13q14 deletion mosaicism". Ophthalmology 110 (10): 1983-8. PMID 14522775.