autosome
C2Pronunciation
UK
- /ˈɔːtəsəʊm/noun
US
- /ˈɔtəˌsoʊm/noun
Description
- Non-sex chromosome
- one of chromosome pairs 1-22
- inherited from both parents
Imagine your cells are like tiny building blocks. Within each block (cell) are blueprints (chromosomes) that determine everything about you—eye color, height, and even a tendency to wiggle your ears! Humans have 46 chromosomes arranged in 23 pairs. All but one of these pairs are called autosomes. These autosomes carry the instructions for all your traits except those related to sex determination (that's where the X and Y chromosomes come in). So, if you're tracing your family history through genetics, you're largely looking at patterns within these autosomal genes.
Think of it like this: 22 out of 23 pairs of blueprints are for building you—the rest determine whether you'll be biologically male or female. Autosomes are essential for normal growth and development, and changes in them can lead to genetic disorders.
Most cells in your body contain 46 chromosomes—thread-like structures made of DNA—and these chromosomes usually come in pairs. Humans typically have 23 pairs, totaling 46 chromosomes. Of these 23 pairs, 22 are called autosomes. The remaining pair is usually the sex chromosomes, typically X and Y (or X and X in people with two X chromosomes), which are most involved in sex determination.
Autosomes contain the vast majority of your genetic information—everything from your hair color and height to your predisposition for certain diseases. They are numbered 1 through 22, generally ordered by size (with chromosome 1 being the largest). Each autosome carries hundreds or even thousands of genes that code for specific traits.
Geneticists study autosomes extensively because mutations or changes in these chromosomes can cause a wide range of genetic disorders, such as cystic fibrosis, sickle cell anemia, and Down syndrome (which involves an extra copy of chromosome 21—an autosome). Understanding how autosomal genes are inherited is crucial for predicting the risk of passing on these conditions to future generations.
Unlike sex chromosomes, which have different versions in males and females, everyone inherits two copies of each autosome—one from their mother and one from their father. This means that traits determined by autosomal genes follow predictable patterns of inheritance based on dominant and recessive alleles.
So, while the sex chromosomes get a lot of attention for determining biological sex, it's the autosomes—those 22 pairs of blueprints—that truly build you, shaping your individual characteristics and influencing your health throughout life.
Examples
- 1
Chromosome types
Humans normally have 22 pairs of autosomes and one pair of sex chromosomes.
Meaning
autosomes
chromosomes that are not sex chromosomes
- 2
Inheritance
The disease gene is on an autosome, so it can be passed on by either parent.
- 3
Gene copies
Unlike genes on the X chromosome, genes on autosomes are usually present in two copies in both males and females.
Forms and spellings
1 form open this card.
Main spelling
- autosomenoun