Human chromosome 13 pair after G-banding. One is from mother, one is from father.
Chromosome 13 pair in human male karyogram.
Features
Length (bp)
113,566,686 bp (CHM13)
No. of genes
308 (CCDS)[1]
Type
Autosome
Centromere position
Acrocentric[2] (17.7 Mbp[3])
Complete gene lists
CCDS
Gene list
HGNC
Gene list
UniProt
Gene list
NCBI
Gene list
External map viewers
Ensembl
Chromosome 13
Entrez
Chromosome 13
NCBI
Chromosome 13
UCSC
Chromosome 13
Full DNA sequences
RefSeq
NC_000013 (FASTA)
GenBank
CM000675 (FASTA)
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.
^Cite error: The named reference CCDS was invoked but never defined (see the help page).
^Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
^Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
Chromosome13 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome13 spans about 113 million...
syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome13. The extra genetic...
A chromosomal abnormality, chromosomal anomaly, chromosomal aberration, chromosomal mutation, or chromosomal disorder is a missing, extra, or irregular...
A chromosome is a package of DNA with part or all of the genetic material of an organism. In most chromosomes, the very long thin DNA fibers are coated...
miscarriage, and the most common extra autosomal chromosomes among live births are 21, 18 and 13. Chromosome abnormalities are detected in 1 of 160 live human...
or all of the large arm of human chromosome13. Depending upon the size and location of the deletion on chromosome13, the physical and mental manifestations...
An autosome is any chromosome that is not a sex chromosome. The members of an autosome pair in a diploid cell have the same morphology, unlike those in...
A karyotype is the general appearance of the complete set of chromosomes in the cells of a species or in an individual organism, mainly including their...
chromatids together during cell division. This constricted region of chromosome connects the sister chromatids, creating a short arm (p) and a long arm...
The Y chromosome is one of two sex chromosomes in therian mammals and other organisms. Along with the X chromosome, it is part of the XY sex-determination...
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate properly during cell division (mitosis/meiosis). There are three...
A ring chromosome is an aberrant chromosome whose ends have fused together to form a ring. Ring chromosomes were first discovered by Lilian Vaughan Morgan...
In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation...
Chromosome 2 is one of the twenty-three pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 2 is the second-largest...
Satellite chromosomes or SAT-chromosomes are chromosomes that contain secondary constructs that serve as identification. They are observed in Acrocentric...
Chromosome 21 is one of the 23 pairs of chromosomes in humans. Chromosome 21 is both the smallest human autosome and chromosome, with 45 million base...
The X chromosome is one of the two sex chromosomes in many organisms, including mammals, and is found in both males and females. It is a part of the XY...
The Philadelphia chromosome or Philadelphia translocation (Ph) is a specific genetic abnormality in chromosome 22 of leukemia cancer cells (particularly...
The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living...
Chromosome 1 is the designation for the largest human chromosome. Humans have two copies of chromosome 1, as they do with all of the autosomes, which are...
A dicentric chromosome is an abnormal chromosome with two centromeres. It is formed through the fusion of two chromosome segments, each with a centromere...
retinoblastoma. In other cases, it is caused by a congenital mutation in the chromosome13 gene 13q14 (retinoblastoma protein). Retinoblastoma is the most intrusive...
an organism has at least one more chromosome than normal, i.e., there may be three or more copies of the chromosome rather than the expected two copies...
Chromosome 15 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 15 spans about 99.7 million...
of chromosome 21 Patau syndrome – trisomy of chromosome13 Edwards syndrome – trisomy of chromosome 18 Klinefelter syndrome – extra X chromosomes in males...
structural abnormality in which the arms of the chromosome are mirror images of each other. The chromosome consists of two copies of either the long (q)...
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