Question

In autosomal recessive inheritance, if both parents are carriers of a gene mutation, there will be...

In autosomal recessive inheritance, if both parents are carriers of a gene mutation, there will be a____ % of disease manifestation in offspring

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answer :

in autosomal recessive inheritance , if both parents are carrier of a gene mutation , there will be a 25% chance of disease manifestation in offspring

Add a comment
Know the answer?
Add Answer to:
In autosomal recessive inheritance, if both parents are carriers of a gene mutation, there will be...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Cystic fibrosis is an autosomal recessive disease caused by a mutation in a single gene with...

    Cystic fibrosis is an autosomal recessive disease caused by a mutation in a single gene with two alleles. Suppose the frequency of cystic fibrosis in a population is 3%. Assuming the gene is in HW equilibrium, calculate the allele and genotype frequencies. If the population consists of 100 individuals, how many are carriers (but unaffected) for the cystic fibrosis allele?

  • A disease that is autosomal recessive, like Cystic Fibrosis, is called autosomal recessive because A.The gene...

    A disease that is autosomal recessive, like Cystic Fibrosis, is called autosomal recessive because A.The gene mutations giving rise to a disease phenotype are located only in offspring and not in parents B.The gene mutations giving rise to a disease phenotype are located on an automatically expressed area in the genome C.The gene mutations giving rise to a disease phenotype are located on sex chromosomes X and/or Y D.The gene mutations giving rise to a disease phenotype are located on...

  • In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance:...

    In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...

  • QUESTION 31 "Both parents are carriers of the allele for Albinism, or lack of the pigment...

    QUESTION 31 "Both parents are carriers of the allele for Albinism, or lack of the pigment melanin in skin or eyes. The equal probability of having male or female offspring with Albinism is 1 afflicted out of every 4 children. This suggests the condition is autosomal recessive X-linked recessive autosomal dominant X-linked dominant

  • 3A) If both parents are heterozygous carriers of a mutant allele, what is the chance that...

    3A) If both parents are heterozygous carriers of a mutant allele, what is the chance that their first child will be homozygous recessive for the mutation? 3B) Parents who are each heterozygous carriers for a recessive mutant allele have a child who does not have the condition. What is the chance this child is a heterozygous carrier of the condition? 3C) If the first child of parents who are both heterozygous carriers of a recessive mutant allele is homozygous recessive,...

  • 4) Cystic fibrosis is a human disease caused by an autosomal recessive mutation. About 1 in...

    4) Cystic fibrosis is a human disease caused by an autosomal recessive mutation. About 1 in 22 people in the human population are heterozygous carriers and have no symptoms of the disease. A woman who has a brother with CF marries a man who has no history of CF in his family a) What are the possible genotypes of the woman? b) What is the most likely genotype of the man? c) What is the percentage of offspring that would...

  • The possible modes of inheritance are autosomal dominant autosomal recessive X-linked recessive mitochondrial inheritance || ITQ...

    The possible modes of inheritance are autosomal dominant autosomal recessive X-linked recessive mitochondrial inheritance || ITQ ? 11 2 3 4 23 TO O | 1 2 3 | | O ■ 2 3 2 3 4 5 Question 1 (12 marks) For the following pedigrees i. identify the most likely mode of inheritance, and ii. describe 2 features that fit with that mode of inheritance. 1 mark each 2 marks each The possible modes of inheritance are autosomal dominant...

  • (10 points) ominant-recessive inheritance pattern, what percentage of the offspring would be homozygous oth parents are...

    (10 points) ominant-recessive inheritance pattern, what percentage of the offspring would be homozygous oth parents are heterozygous for the gene?

  • Hemophilia A is a genetic disorder of recessive X chromosome mutation of the Factor VIII gene...

    Hemophilia A is a genetic disorder of recessive X chromosome mutation of the Factor VIII gene that causes a blood clotting protein Factor VIII missing or deficient. If a person with XY chromosomes is affected by Hemophilia A and a person with XX chromosomes is an unaffected person, what is the probability that their male offspring might be hemophilic and what is the probability that their female offspring might be carriers of the mutated gene?

  • Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked...

    Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked 2) indicate whether the transmission appears dominant or recessive 3) provide at least two characteristics for each that support your conclusion. In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT