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  2. List of organisms by chromosome count - Wikipedia

    en.wikipedia.org/wiki/List_of_organisms_by...

    17. Yellow dung fly. (Scathophaga stercoraria) 12. 10 autosomal and 2 allosomic (sex) chromosomes. Males have XY sex chromosomes and females have XX sex chromosomes. The sex chromosomes are the largest chromosomes and constitute 30% of the total length of the diploid set in females and about 25% in males.

  3. Chromosome - Wikipedia

    en.wikipedia.org/wiki/Chromosome

    This is an accepted version of this page This is the latest accepted revision, reviewed on 15 October 2024. DNA molecule containing genetic material of a cell This article is about the DNA molecule. For the genetic algorithm, see Chromosome (genetic algorithm). Chromosome (10 7 - 10 10 bp) DNA Gene (10 3 - 10 6 bp) Function A chromosome and its packaged long strand of DNA unraveled. The DNA's ...

  4. Genome - Wikipedia

    en.wikipedia.org/wiki/Genome

    t. e. An image of the 46 chromosomes making up the diploid genome of a human male (the mitochondrial chromosomes are not shown). In the fields of molecular biology and genetics, a genome is all the genetic information of an organism. [ 1 ] It consists of nucleotide sequences of DNA (or RNA in RNA viruses).

  5. Ploidy - Wikipedia

    en.wikipedia.org/wiki/Ploidy

    Euploidy (Greek eu, "true" or "even") is the state of a cell or organism having one or more than one set of the same set of chromosomes, possibly excluding the sex-determining chromosomes. For example, most human cells have 2 of each of the 23 homologous monoploid chromosomes, for a total of 46 chromosomes.

  6. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a phenotypic male at birth has an extra X chromosome. [ 10 ] These complications commonly include infertility and small, poorly functioning testicles (if present). These symptoms are often noticed only at puberty, although this is one of the most common chromosomal ...

  7. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    The fundamental autosomal number or autosomal fundamental number, FNa[36]or AN,[37]of a karyotype is the number of visible major chromosomal arms per set of autosomes(non-sex-linked chromosomes). Ploidy. [edit] Ploidyis the number of complete sets of chromosomes in a cell. Polyploidy, where there are more than two sets of homologous chromosomes ...

  8. Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Turner_syndrome

    Henry Turner. Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which females cells have only one X chromosome or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome. [ 2 ][ 6 ][ 7 ] Most ...

  9. DNA - Wikipedia

    en.wikipedia.org/wiki/DNA

    The set of chromosomes in a cell makes up its genome; the human genome has approximately 3 billion base pairs of DNA arranged into 46 chromosomes. [96] The information carried by DNA is held in the sequence of pieces of DNA called genes. Transmission of genetic information in genes is achieved via complementary base pairing. For example, in ...