Kingdom
Organisms that belong to the same class must belong to the same animal
kingdom
Answer:
Nonsense mutation: it causes a premature stop codon, so the protein cannot be fully synthesized.
Missense mutation: it causes change on the aminoacid encoded, so it can cause a change in the protein structure if the new aminoacid doesn't have the same chemichal properties as the original.
Synonymous (silent) mutation: it causes no change, the same aminoacid is encoded.
Single nucleotide insertion or deletion: changes the entire structure of the protein because it shifts the reading frame.
Three nucleotide deletion: one aminoacid will no longer be part of the protein, if this aminoacid was located, for example, on the active site of an enzyme, the protein could lose its function.
Chromosomal translocation: it can break a gene in two, causing the protein to no longer be able to be synthesized, or it can change the transcription regulation because it is now under the effect of other regulating sites that result in a different transcription pattern.
Answer:
a. Trisomic
Explanation:
A trisomy is a genomic phenomenon whereby a particular chromosome is present in three copies. In this case, the trisomy involves the chromosome P, being this species a tetraploid with 5 pairs of homologous chromosomes (2n = 10). In humans, the trisomy for chromosome 21 is one of the most common types of aneuploidies that lead to the Down syndrome by producing alterations in gene expression patterns that are associated with changes in the phenotype
<span>A positive tropism is a plant's growth response ________ the stimulus.
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Answer: Toward
Answer:
Explanation:
A woman who is a carrier for #1 hemophilia and a man that does not have the
condition have children. What is the probability that they will have a child
with the condition being studied? What is the gender of that child?
if the baby gets the Y chromosome from the father it will be a boy. If the boy gets his mother's X chromosome with the hemophilia gene he will have hemophilia. If he inherits his mother's other X chromosome, he will have normal blood clotting. If the baby gets the X chromosome from the father it will be a girl.
#4 A woman that is heterozygous for type A blood and a man that is heterozygous for type B blood have children. What are the possible blood types of their children?
One parent with A and another with B can produce a child with A, B, AB or O blood types.
#5 Two people are both unknowingly carriers for the cystic fibrosis gene. What is the probability that they will have children with cystic fibrosis?
If both parents are carriers there is a 1 in 4 (25 percent) chance that both will pass on the non-functioning gene, which would result in a pregnancy affected with cystic fibrosis.
#3 A woman that is heterozygous for Huntington's disease and a man that does not have the condition have children . What is the probability that their children inherit the Huntington's gene ?
Huntington's disease (HD) is what is called a dominant genetic disease. What this usually means is that a child only has a chance of getting a disease like this if a parent has it too. But parents without HD can have a child with HD. This is true of any dominant genetic disease
