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Punnett square: If the other parent does not have the recessive genetic disposition, it does not appear in the phenotype of the children, but on the average 50% of them become carriers. A hereditary carrier ( genetic carrier or just carrier ), is a person or other organism that has inherited a recessive allele for a genetic trait or mutation ...
A Punnett square showing a typical test cross. (green pod color is dominant over yellow for pea pods [1] in contrast to pea seeds, where yellow cotyledon color is dominant over green [2]). Punnett squares for each combination of parents' colour vision status giving probabilities of their offsprings' status, each cell having 25% probability in ...
Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]
A. Abdallat–Davis–Farrage syndrome; Abetalipoproteinemia; Absent tibia-polydactyly-arachnoid cyst syndrome; Acanthosis nigricans-muscle cramps-acral enlargement syndrome
An example of a family pedigree displaying an autosomal recessive trait. A pedigree is a diagram showing the ancestral relationships and transmission of genetic traits over several generations in a family. Square symbols are almost always used to represent males, whilst circles are used for females.
Punnett squares showing typical test crosses and the two potential outcomes. The individual in question may either be heterozygous, in which half the offspring would be heterozygous and half would be homozygous recessive, or homozygous dominant, in which all the offspring would be heterozygous.
Punnett square for the agouti gene in mice, demonstrating a recessive lethal allele. [2] Lethal alleles were first discovered by Lucien Cuénot in 1905 while studying the inheritance of coat colour in mice. The agouti gene in mice is largely responsible for determining coat colour. The wild-type allele produces a blend of yellow and black ...
In medical genetics, compound heterozygosity is the condition of having two or more heterogeneous recessive alleles at a particular locus that can cause genetic disease in a heterozygous state; that is, an organism is a compound heterozygote when it has two recessive alleles for the same gene, but with those two alleles being different from each other (for example, both alleles might be ...