Almost 100% sure that they're called carriers.
I don't know and don't care
PAI-1 heterozygous is an inherited blood disorder from ONE parent-ONE copy of the gene. PAI-1 Homozygous is an inherited blood disorder from BOTH parents-TWO copies of the gene.
an allele that is not expressed when paired with a dominant allele. Only expressed when paired with another recessive allele.
Blue eyes - homozygous recessive Brown eyes - homozygous dominant Brown eyes with one brown allele and one blue allele - heterozygous
Mutations in sex cells can be passed on to children. Mutations in sex cells only affect offspring. Mutations in sex cells do not affect the organism.
I don't know and don't care
A carrier of a genetic disorder who does not show symptoms is most likely to be heterozygous for the trait and able to transmit it to his offspring. The term heterozygous refers to a pair of gene with one dominant trait and one recessive trait.
yes it can skip a generation, since it is a Mendel inheritance. and it is a reccesive trait. therefore offspring's can have two unaffected parents but chances are both parents might be carriers
Yes. Heterozygous dominance offers a way to preserve the mutated allele.
Sickle Cell Anemia, in it's heterozygous form it does not present as the disease and it gives the carrier resistance to malaria.
It will be all about the gains and shreins
Mutation is any change in the genetic code of an individual regardless of how the change manifests. A genetic disorder is the result of an unfavorable mutation that results through through heterozygous recessive parents producing a homozygous recessive offspring, a random dominant mutation, or multiple polygenic mutations that compound for a negative effect on an individual as examples.
If a genetic disorder is carried on a recessive gene, offspring will only have the disorder if both parents have the recessive gene.
PAI-1 heterozygous is an inherited blood disorder from ONE parent-ONE copy of the gene. PAI-1 Homozygous is an inherited blood disorder from BOTH parents-TWO copies of the gene.
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.
Dominant disorders can be passed onto the offspring if the dominant gene is present in the offspring.
The answer depends on the genes of the parents and further ancestors.