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autosomal$6124$ - перевод на Английский
![[[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome](https://commons.wikimedia.org/wiki/Special:FilePath/Klippel–Feil syndrome and Sprengel's deformity.png?width=200 "[[CT scan]] showing fused [[cervical vertebrae]] and [[Sprengel's deformity]] (arrow), as seen in Klippel–Feil syndrome")
![Hereditary defects in [[enzymes]] are generally inherited in an autosomal fashion because there are more non-X chromosomes than X-chromosomes, and a recessive fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal recessive inheritance for affected enzyme.png?width=200 "Hereditary defects in [[enzymes]] are generally inherited in an autosomal fashion because there are more non-X chromosomes than X-chromosomes, and a recessive fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers.")
![dominant-negative]] process, wherein a mutated gene product adversely affects the non-mutated gene product within the same cell.](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal dominant inheritance for structural protein.png?width=200 "dominant-negative]] process, wherein a mutated gene product adversely affects the non-mutated gene product within the same cell.")
Определение
Википедия
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 allosomal (sex chromosome) pairs, which may have different structures. The DNA in autosomes is collectively known as atDNA or auDNA.
For example, humans have a diploid genome that usually contains 22 pairs of autosomes and one allosome pair (46 chromosomes total). The autosome pairs are labeled with numbers (1–22 in humans) roughly in order of their sizes in base pairs, while allosomes are labelled with their letters. By contrast, the allosome pair consists of two X chromosomes in females or one X and one Y chromosome in males. Unusual combinations of XYY, XXY, XXX, XXXX, XXXXX or XXYY, among other Salome combinations, are known to occur and usually cause developmental abnormalities.
Autosomes still contain sexual determination genes even though they are not sex chromosomes. For example, the SRY gene on the Y chromosome encodes the transcription factor TDF and is vital for male sex determination during development. TDF functions by activating the SOX9 gene on chromosome 17, so mutations of the SOX9 gene can cause humans with an ordinary Y chromosome to develop as females.
All human autosomes have been identified and mapped by extracting the chromosomes from a cell arrested in metaphase or prometaphase and then staining them with a type of dye (most commonly, Giemsa). These chromosomes are typically viewed as karyograms for easy comparison. Clinical geneticists can compare the karyogram of an individual to a reference karyogram to discover the cytogenetic basis of certain phenotypes. For example, the karyogram of someone with Patau Syndrome would show that they possess three copies of chromosome 13. Karyograms and staining techniques can only detect large-scale disruptions to chromosomes—chromosomal aberrations smaller than a few million base pairs generally cannot be seen on a karyogram.
