Red-green color blindness is caused by a mutation in the gene coding for one the Ospin proteins which are needed for color Vision the diagram in the image shows the inheritance of red-green color blindness in one family.  person 12 is pregnant with her forth child, what is the probability that this child will be a male with red-green color blindness explain the answer by drawing a genetic diagram using the following symbols in the second image.

Q: The picture below represents a G1 cell from a newly discovered species that uses the X/Y sex…

A: The cell is in G1 phase and hence it undergoes the S phase to duplicate the DNA. Thus, homologous…

Q: X-linked, recessive disorder in which muscles waste away early in life, resulting in death in the…

A: X linked inheritance is a type of sex linked inheritance in which mutation occurs in one of the X…

Q: Using a particular family as a model, how do you distinguish nuclear from extrachromosomal…

A: Distinguish nuclear inheritance from extrachromosomal inheritance.

Q: A defective gene on chromosome 15 causes Tay-Sachs disease. It is a central nervous system…

A: Given: A pedigree. A defective gene on chromosome 15 causes Tay-Sachs disease. Individual III - 1 -…

Q: (A) Which of the above offspring are recombinant? (B) What is the map distance between the genes?

A: ANSWER1. Recombinants: These are those offspring that have traits different from their parents.…

Q: estions below all refer to the following pedigree. The locus for allele D/d determines how cilia on…

A: It is evident that the trait is not sex-linked because:-   In the case of Y-linked disorders, only…

Q: What are the possible genotypes for the following wizards for the MC1R gene? I:…

A: Genetic Inheritance: The genes from parents regulating different traits are passed down to offspring…

Q: 1 2 3 4 5 i、月 6 8 9 10 11 12 13 14 15 16 17 18 19 20 Y 21 22

A: Karyotyping is the process by which photographs of chromosomes are taken in order to determine the…

Q: The questions below all refer to the following pedigree. The locus for allele D/d determines how…

A:

Q: Give the phenotypic effects and chromosomal aberrations of the following syndromes/disorders: Down…

A: DOWN SYNDROME. Down syndrome is the most common chromosomal disorder due to the autosomal trisomy of…

Q: The following pedigree shows a pattern of inheritance that is found in which of the following…

A:

Q: As shown in the Punnett square below, one variety of deafness is caused by an autosomal recessive…

A: An autosomal recessive disorder is defined as a condition or state in which two copies of an…

Q: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a disorder that affects the normal function…

A: Note : As per Bartleby Guidelines, For Remaining Answers Please Repost The Question. Introduction:…

Q: Pedigree information regarding the incidence of Tay-Sachs within a family is depicted above. The row…

A: Human beings are diploid organisms, i.e., hey have two sets of chromosomes. Humans carry 22 pairs of…

Q: A possible explanation for the increased incidence of Tay-Sachs disease among Ashkenazi Jews is

A: Tay Sachs is a rare autosomal recessive disorder that causes mental and physical disabilities…

Q: Explore chromosomal defects among humans in Ensembl at…

A: Defects in the structure or quantity of chromosomes in a person's cells are referred to as…

Q: A defective gene on chromosome 15 causes Tay-Sachs disease. It is a central nervous system…

A: Tay-Sachs disease is an inherited disorder that results in progressive destruction of nerve cells in…

Q: Draw a Punnett square for the dihybrid cross. There are two known alleles of gene occupying a…

A: Dihybrid cross involves two genes in a cross. That's why the two traits are involved in this cross.

Q: The pedigree below shows the inheritance pattern of a rare X-linked allele for one family. The…

A: Pedigree is a family chart where genetic councillor put some symbol for easy description of a…

Q: The orange coat color allele in cats is located on the X chromosome and is one of two genes…

A: The two variants of coat color found in cats are orange and black. The alleles responsible for these…

Q: If the mutation occurred in Jonathan's somatic cells when he was in his 30's, what type of alleles…

A: A neurodegenerative condition that is primarily inherited is Huntington's disease (HD), also known…

Q: Which statement about the relationship between genetic map and physical map is FALSE? The…

A: Genetic Map: A genetic map, also referred to as a linkage map, illustrates the relative positions of…

Q: Jeff's spermatogonium (precursor sperm cell before meiosis) looks like the cell on the left (only…

A: The improper separation of the sister chromatids or the homologous chromosomes during meiosis leads…

Q: Please answer question (a) (b) and (e)

A: Crossing over increases variations.

Q: 1 In humans, red-green colorblindness is a sex-linked recessive condition. Show a cross between a…

A: Note - Since you have asked multiple questions, we will solve the first question for you. If you…

Q: One of the people on the chart is labeled with the letter A. Which of the following statements…

A: The genes located on the nuclear chromosomes obey the Mendelian law of inheritance. In the human…

Q: Look at the pedigree below and answer the following questions related to the human genetic trait…

A: A pedigree or family tree is made up of symbols and lines that indicates or represents genetic…

Q: A child with the genes for PKU (a recessive disorder that leads to brain damage because proteins…

A: Phenylketonuria (PKU) is a genetic disorder. In this condition the gene for the enzyme phenylalanine…

Q: An organism has the genotype a"g*/a"g*;qt"/qtt;rth*/rth+. Indicate the correct genes/ alleles at all…

A: Chromosome X 1:a- 2:g+ 3:a- 4:g+

Q: An extra finger in humans is rare but is due to a dominant gene. When one parent is normal and the…

A: Polydactyly, which is having an additional finger, is controlled by a dominant gene. This implies…

Q: Consult Figure 1, which shows a human karyotype with chromosomes arranged in order of decreasing…

A: Eukaryotes usually have their genetic material packed and condensed into chromosomes and stored…

Q: CIUSS Out An organism has the genotype a"g*/a"g* ; q"f"/g+f";r+h+/r+h+. Indicate the correct genes/…

A: The alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: Below is a pedigree chart for a family that has a history of Alkaptonuria.   Individuals infected…

A: Pedigree analysis is a method to identify the inheritance of a genetic trait across generations.…

Q: Duchenne Muscular Dystrophy (DMD) is a disease that manifests in muscle weakness. It exhibits…

A: The mutation is the change in the nucleotide sequence that codes for the phenotype in an organism.…

Q: L, R, P and D are four genes located on the same chromosome in a diploid organism. Map distances…

A: Genetic mapping is a technique to determine the relative position of genes on a chromosome and their…

Q: An abnormality of the large intestine called intestinal polyposis (IP) is dependent on dominant gene…

A: Genes, the hereditary units of genetic material can exist in two versions called alleles which are…

Q: harcot-Marie-Tooth disease (CMT)causes motor and sensory europathies of the peripheral nervous…

A: Mitofusin protein which is encoded by  MFN and play a very important role in regulations of…

Q: his area of the chromosome iIS 5%.

A: Introduction  Linkage disequilibrium (LD) is the nonrandom relationship of alleles of various loci.…

Q: Part of the karyotype of a diploid individual who is heterozygous for one chromosomal rearrangement…

A: Chromosomal rearrangements are structural changes to chromosomes that affect how the genetic…

Q: A defective gene on chromosome 15 causes Tay-Sachs disease. It is a central nervous system…

A: Many genetic disorders are inherited in different patterns. They can be Autosomal or sex-linked.…

Q: The picture below represents a G1 cell from a newly discovered species that uses the X/Y sex…

A: Meiosis results in the formation of four haploid cells from one diploid cell.

Q: A 43-year-old (gravida 2, para 2) pregnant woman requests chorionic villus sampling (CVS) and a…

A: The correct answer is b. Klinefelter syndrome is a diagnosis for a boy with mild to moderate…

Q: Uniparental disomy (UPD) occurs when both chromosomes of a pair or areas from one chromosome in any…

A: The question pertains to the concept of genetic mosaicism, which is a phenomenon that occurs when…

Communication

Communication is a method of transferring information between two persons or organisms. Communication is possible using mutually understood behaviors such as signs, symbols, or language. In the year 1980, S. F. Scudder proposed communication theory. According to his ideas, all living beings on the earth communicate, but the methods of communication differ. Communication skills are now part of soft skills.