In humans, the glucose-6-phosphate dehydrogenase (G6PD) gene involved in sugar metabolism is X-linked. The dominant allele (G) codes for fast enzymes for normal cell functioning while the recessive allele (g) codes for slow enzymes, which are responsible for the reduced enzymatic activity of cells. However, the presence of slow enzymes has minimal effect in the overall functioning of heterozygotes, thus normal. Recessives, however, are more prone to oxidative reactions that speed up the cell damaging process, thus weak (but not lethal). If random inactivation occurs during dosage compensation, what would be the genotypes and phenotypes of the children of a heterozygous mother and a recessive father? Show the complete cross.

In humans, the glucose-6-phosphate dehydrogenase (G6PD) gene involved in sugar metabolism is X-linked. The dominant allele (G) codes for fast enzymes for normal cell functioning while the recessive allele (g) codes for slow enzymes, which are responsible for the reduced enzymatic activity of cells. However, the presence of slow enzymes has minimal effect in the overall functioning of heterozygotes, thus normal. Recessives, however, are more prone to oxidative reactions that speed up the cell damaging process, thus weak (but not lethal). If random inactivation occurs during dosage compensation, what would be the genotypes and phenotypes of the children of a heterozygous mother and a recessive father? Show the complete cross.

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter11: Genome Alterations: Mutation And Epigenetics

Section: Chapter Questions

Problem 16QP: Familial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior...

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In humans, the glucose-6-phosphate dehydrogenase (G6PD) gene involved in sugar metabolismis X-linked. The dominant allele (G) codes for fast enzymes for normal cell functioning while the recessiveallele (g) codes for slow enzymes, which are responsible for the reduced enzymatic activity of cells.However, the presence of slow enzymes has minimal effect in the overall functioning of heterozygotes,thus normal. Recessives, however, are more prone to oxidative reactions that speed up the celldamaging process, thus weak (but not lethal). If random inactivation occurs during dosage compensation,what would be the genotypes and phenotypes of the children of a heterozygous mother and a recessivefather?
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Anhidrotic ectodermal dysplasia is an X-linked recessive disorder in humans characterized by small teeth, no sweat glands, and sparse body hair. This trait is usually seen in men, but women who are heterozygous carriers of the trait often have irregular patches of skin with few or no sweat glands (see the illustration below). Q. Explain why women who are heterozygous carriers of a recessive gene for anhidrotic ectodermal dysplasia have irregular patches of skin lacking sweat glands.
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Anhidrotic ectodermal dysplasia is an X-linked recessive disorder in humans characterized by small teeth, no sweat glands, and sparse body hair. This trait is usually seen in men, but women who are heterozygous carriers of the trait often have irregular patches of skin with few or no sweat glands (see the illustration below). a. Explain why women who are heterozygous carriers of a recessive gene for anhidrotic ectodermal dysplasia have irregular patches of skin lacking sweat glands. b. Why does the distribution of the patches of skin lacking sweat glands differ among the females depicted in the illustration, even between the identical twins?
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Let’s suppose that two different X-linked genes exist in mice,designated with the letters N and L. Gene N exists in a dominant,normal allele and in a recessive allele, n, that is lethal. Similarly,gene L exists in a dominant, normal allele and in a recessive allele,l, that is lethal. Heterozygous females are normal, but males thatcarry either recessive allele are born dead. Explain whether or notit would be possible to map the distance between these two genesby making crosses and analyzing the number of living and deadoffspring. You may assume that you have strains of mice in whichfemales are heterozygous for one or both genes.
The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red eyes, miniature wings are recessiveto long wings, and sable body is recessive to gray body. A cross wasmade between wild-type males with red eyes, long wings, and graybodies and females with vermilion eyes, miniature wings, and sablebodies. The heterozygous female offspring from this cross, whichhad red eyes, long wings, and gray bodies, were then crossed tomales with vermilion eyes, miniature wings, and sable bodies. Thefollowing data were obtained for the F2 generation (including bothmales and females):1320 vermilion eyes, miniature wings, sable body1346 red eyes, long wings, gray body102 vermilion eyes, miniature wings, gray body90 red eyes, long wings, sable body42 vermilion eyes, long wings, gray body48 red eyes, miniature wings, sable body2 vermilion eyes, long wings, sable body1 red eyes, miniature wings, gray bodyAnalyze data. Make a drawing. Make a calculation.
The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red eyes, miniature wings are recessiveto long wings, and sable body is recessive to gray body. A cross wasmade between wild-type males with red eyes, long wings, and graybodies and females with vermilion eyes, miniature wings, and sablebodies. The heterozygous female offspring from this cross, whichhad red eyes, long wings, and gray bodies, were then crossed tomales with vermilion eyes, miniature wings, and sable bodies. Thefollowing data were obtained for the F2 generation (including bothmales and females):1320 vermilion eyes, miniature wings, sable body1346 red eyes, long wings, gray body102 vermilion eyes, miniature wings, gray body90 red eyes, long wings, sable body42 vermilion eyes, long wings, gray body48 red eyes, miniature wings, sable body2 vermilion eyes, long wings, sable body1 red eyes, miniature wings, gray bodyWhat topic in genetics does this question address?
The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red eyes, miniature wings are recessiveto long wings, and sable body is recessive to gray body. A cross wasmade between wild-type males with red eyes, long wings, and graybodies and females with vermilion eyes, miniature wings, and sablebodies. The heterozygous female offspring from this cross, whichhad red eyes, long wings, and gray bodies, were then crossed tomales with vermilion eyes, miniature wings, and sable bodies. Thefollowing data were obtained for the F2 generation (including bothmales and females):1320 vermilion eyes, miniature wings, sable body1346 red eyes, long wings, gray body102 vermilion eyes, miniature wings, gray body90 red eyes, long wings, sable body42 vermilion eyes, long wings, gray body48 red eyes, miniature wings, sable body2 vermilion eyes, long wings, sable body1 red eyes, miniature wings, gray bodyA. Calculate the map distances separating the three genes.B. Is…
In Drosophila, the X-linked recessive mutation vermilion (v) causes bright red eyes, in contrast to the brick-red eyes of wild type. A separate autosomal recessive mutation, suppressor of vermilion (su-v), causes flies homozygous or hemizygous for v to have wildtype eyes. In the absence of vermilion alleles, su-v has no effect on eye color. Determine the F1 and F2 phenotypic ratios from a cross between a female with wild-type alleles at the vermilion locus, but who is homozygous for su-v, with a vermilion male who has wildtype alleles at the su-v locus