Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Alternate form of the same genes are called
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- A recessive maternal effect mutant in zebrafish, called ichabod, results in embryos lacking heads that are non-viable. You have been instructed to identify females that are homozygous for the ichabod mutant allele. At your disposal are a tank of wild-type fish (males and females), a tank of male and female parental fish that are all heterozygous for the ichabod mutant allele (ichabodl+), and a tank of F1 fish derived from a cross between a heterozygous male and heterozygous female (ichabodl+). Which of the following would be a way to identify females that are homozygous mutant, i.e. ichabodlichabod? Select all answers that would work. Cross F1 females to F1 males and observe their offspring. Crosses that produce headless offspring came from a homozygous female. a. Cross F1 males to females from the parental tank and observe their offspring. 25% of these crosses should produce headless offspring. b. Cross F1 females to F1 males to make the F2 generation. Cross F2 females to F2 males and…arrow_forwardwhat is linkage in geneticsarrow_forwardGenes on one gene that affect the expression of genes at different locations are said to be alleles epistatic continuous linkedarrow_forward
- A wrinkle-seeded plant (rr) is crossed with round-seeded (Rr).arrow_forwardHow are alleles of particular gene differ from each other?explain its significance?arrow_forwardThe following normal human sister chromosomes DO NOT necessarily have in common with each other: Same Genes, Same Size, Same Alleles, Same Banding Pattern.arrow_forward
- In case of the human blood type, the gene that produces the enzyme responsible for attaching the A carbohydrate is equally dominant to the gene that produces the enzyme that attaches to B carbohydrate what is this called?arrow_forwardPhenylketonuria is one of the most common recessive genetic disorders in humans. Infants with PKU are missing an enzyme called phenylalanine hydroxylase, needed to break down an amino acid called phenylalanine. If a strict diet that minimizes the amount of phenylalanine in the diet is not followed, a severe nervous disorder may result. If two heterozygous parents have a child, hah is the possible genotype and phenotype for this individual?arrow_forwardExplain the reason whether the genetic information from two sister chromatids is passed from a single parent or both the parents.arrow_forward
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