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Zygosity (the noun, zygote, is from the Greek zygotos "yoked," from zygon "yoke") (/ zaɪˈɡɒsɪti /) is the degree to which both copies of a chromosome or gene have the same genetic sequence. In other words, it is the degree of similarity of the alleles in an organism. Most eukaryotes have two matching sets of chromosomes; that is, they are ...
Allele. An allele[1], or allelomorph, is a variant of the sequence of nucleotides at a particular location, or locus, on a DNA molecule. [2] Alleles can differ at a single position through single nucleotide polymorphisms (SNP), [3] but they can also have insertions and deletions of up to several thousand base pairs. [4]
An autosome is any chromosome other than a sex chromosome. In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. [1][2] The first variant is termed dominant and the second is called recessive.
Genetic characteristics have alternate forms, each inherited from one of two parents. Today these are called alleles. One allele is dominant over the other. The phenotype reflects the dominant allele. Gametes are created by random segregation. Heterozygotic individuals produce gametes with an equal frequency of the two alleles.
Category. v. t. e. The genotype of an organism is its complete set of genetic material. [1] Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. [2] The number of alleles an individual can have in a specific gene depends on the number of copies of each chromosome found in ...
A haplotype (haploid genotype) is a group of alleles in an organism that are inherited together from a single parent. [1][2] Many organisms contain genetic material (DNA) which is inherited from two parents. Normally these organisms have their DNA organized in two sets of pairwise similar chromosomes. The offspring gets one chromosome in each ...
The simplest genetic model involves a single locus with two alleles (b and B) affecting one quantitative phenotype. The number of B alleles can be 0, 1, or 2. For any genotype, ( B i , B j ), where B i and B j are either 0 or 1, the expected phenotype can then be written as the sum of the overall mean, a linear effect, and a dominance deviation ...
Autosomal traits are associated with a single gene on an autosome (non-sex chromosome)—they are called "dominant" because a single copy—inherited from either parent—is enough to cause this trait to appear. This often means that one of the parents must also have the same trait, unless it has arisen due to an unlikely new mutation.