Autosome - Wikipedia
An autosome is a chromosome that is not an allosome (a sex chromosome). The members of an autosome pair in a diploid cell have the same morphology, unlike those in allosome 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 ...
Autosome | Definition of Autosome by Merriam-Webster
Autosome definition is - a chromosome other than a sex chromosome. Recent Examples on the Web. Law enforcement also tested 20 or so genetic markers from autosomes—nonsex chromosomes, which are inherited from both parents. — Allysia Finley, WSJ, "The Making of a DNA Detective," 15 Feb. 2019 The rest, the autosomes, comes from all of one’s ancestors.
Autosome | biology | Britannica.com
In heredity: Sex linkage …other pairs of chromosomes (called autosomes). The members of the autosome pairs are truly homologous; that is, each member of a pair contains a full complement of the same genes (albeit, perhaps, in different allelic forms).
Autosome - Definition and Function of Autosomes | Biology ...
Autosome Definition. An autosome is a chromosome in a eukaryotic cell that is not a sex chromosome.. Unlike prokaryotic cells, eukaryotic cells have many chromosomes in which they package their DNA. This allows eukaryotes to store much more genetic information.
Autosomal | Define Autosomal at Dictionary.com
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Autosomal | Definition of Autosomal by Merriam-Webster
: of, belonging to, located on, or transmitted by an autosome autosomal genes/inheritance autosomal dominant/recessive disorders … a genetic disorder that is passed down in autosomal recessive fashion—in other words, you have to inherit an abnormal gene from each parent for the trait to appear.
OptiGen - Phosphofructokinase (PFK) Test - canine genetic ...
Breed Links ; Phosphofructokinase (PFK) is an enzyme that is crucial for production of energy from sugar sources in all cells of the body, especially red blood cells and muscle cells.
Tetra-amelia syndrome - Wikipedia
Tetra-amelia syndrome (tetra-+ amelia), also called autosomal recessive tetraamelia, is an extremely rare autosomal recessive congenital disorder characterized by the absence of all four limbs. Other areas of the body are also affected by malformations, such as the face, skull, reproductive organs, anus and pelvis. The disorder is caused by mutations in the WNT3 gene.
A - D Archives - Genographic Project
Terms. Allele. Autosome. Base. Cell. Chromosome. Darwin, Charles. DNA. Double Helix. Definitions. Allele. An allele is a variant form of a gene. When a genes varies (genes for eye color, for example, could be blue or brown) each individual form is called an allele.
Glossary - PBS: Public Broadcasting Service
acquired trait: A phenotypic characteristic, acquired during growth and development, that is not genetically based and therefore cannot be passed on to the next generation (for example, the large ...