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  2. Locus (genetics) - Wikipedia

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

    (4) Long (q) arm 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 ...

  3. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]

  4. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    CM000680 ( FASTA) Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells .

  5. Chromosomal translocation - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_translocation

    In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal, and Robertsonian translocation. Reciprocal translocation is a chromosome abnormality caused by exchange of parts between non-homologous chromosomes.

  6. Robertsonian translocation - Wikipedia

    en.wikipedia.org/wiki/Robertsonian_translocation

    Robertsonian translocation ( ROB) is a chromosomal abnormality where the entire long arms of two different chromosomes become fused to each other. It is the most common form of chromosomal translocation in humans, affecting 1 out of every 1,000 babies born. [1] It does not usually cause medical problems, though some people may produce gametes ...

  7. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Medical genetics. Proximal 18q- is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [1] Exact breakpoints vary.

  8. Chromosome regions - Wikipedia

    en.wikipedia.org/wiki/Chromosome_regions

    The largest regions on each chromosome are the short arm p and the long arm q, separated by a narrow region near the center called the centromere. Other specific regions have also been defined, some of which are similarly found on every chromosome, while others are only present in certain chromosomes. Named regions include: Arms (p and q ...

  9. Chromatid - Wikipedia

    en.wikipedia.org/wiki/Chromatid

    Once the paired sister chromatids have separated from one another (in the anaphase of mitosis) each is known as a daughter chromosome. The short arm of the right chromatid (3), and the long arm of the right chromatid (4), are also marked. Schematic karyogram of the human chromosomes, showing their usual state in the G 0 and G 1 phase of the ...