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  2. Locus (genetics) - Wikipedia

    en.wikipedia.org/wiki/Locus_(genetics)

    In genetics, a locus (pl.: loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located. [1] Each chromosome carries many genes, with each gene occupying a different position or locus; in humans, the total number of protein-coding genes in a complete haploid set of 23 chromosomes is estimated at ...

  3. Gene mapping - Wikipedia

    en.wikipedia.org/wiki/Gene_mapping

    Gene maps help describe the spatial arrangement of genes on a chromosome. Genes are designated to a specific location on a chromosome known as the locus and can be used as molecular markers to find the distance between other genes on a chromosome. Maps provide researchers with the opportunity to predict the inheritance patterns of specific ...

  4. Chromosome - Wikipedia

    en.wikipedia.org/wiki/Chromosome

    This is an accepted version of this page This is the latest accepted revision, reviewed on 8 February 2025. 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 ...

  5. Genetic linkage - Wikipedia

    en.wikipedia.org/wiki/Genetic_linkage

    The recombination frequency will be 50% when two genes are located on different chromosomes or when they are widely separated on the same chromosome. This is a consequence of independent assortment. [citation needed] When two genes are close together on the same chromosome, they do not assort independently and are said to be linked.

  6. Genetic marker - Wikipedia

    en.wikipedia.org/wiki/Genetic_marker

    A genetic marker is a gene or DNA sequence with a known location on a chromosome that can be used to identify individuals or species.It can be described as a variation (which may arise due to mutation or alteration in the genomic loci) that can be observed.

  7. Pseudoautosomal region - Wikipedia

    en.wikipedia.org/wiki/Pseudoautosomal_region

    The SHOX gene in the PAR1 region is the gene most commonly associated with and well understood with regards to disorders in humans, [17] but all pseudoautosomal genes escape X-inactivation and are therefore candidates for having gene dosage effects in sex chromosome aneuploidy conditions (45,X, 47,XXX, 47,XXY, 47,XYY, etc.).

  8. Gene - Wikipedia

    en.wikipedia.org/wiki/Gene

    The gene is located on an autosomal chromosome. The white allele is recessive to the blue allele. The probability of each outcome in the children's generation is one quarter, or 25 percent.

  9. Lists of human genes - Wikipedia

    en.wikipedia.org/wiki/Lists_of_human_genes

    •List of human protein-coding genes page 2 covers genes EPHA1–MTMR3 •List of human protein-coding genes page 3 covers genes MTMR4–SLC17A7 •List of human protein-coding genes page 4 covers genes SLC17A8–ZZZ3 NB: Each list page contains 5000 human protein-coding genes, sorted alphanumerically by the HGNC-approved gene symbol.