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75 Cards in this Set

  • Front
  • Back

A diploid cell of baker's yeast has 32 chromosomes. How many chromosomes are in each of its haploid spores?

16

When do homologous chromosomes separate from one another?

during meiosis 1

In cystic fibrosis, which of the following is/are affected?

airways


digestive system


reproductive system

Every person has _____ alleles of the CFTR gene.

2

A meiotic error occurred during gamete formation resulting in an egg that has 24 chromosomes. If that egg is fertilized by a normal sperm, how many chromosomes will be in the zygote?

47

What is the genotype of a person with CF?

homozygous recessive

A woman has cystic fibrosis. Therefore:

she must have inherited a cystic fibrosis allele from both her mother and her father

In meiosis, sister chromatids separate during:

meiosis 2

A gene encodes a protein of 350 amino acids. A mutation creates an allele that only has the first 120 amino acids. What could happen to this mutant allele?

The protein encoded by the mutant allele is shorter than the one encoded by the normal allele.




The protein encoded by the mutant allele could be non-functional.




The mutant allele could be associated with disease.

`Allele A has 235 codons. Allele a (an alternative allele of the same gene) has 233 codons. When comparing the protein encoded by allele A to that encoded by allele a, protein A must be:

longer by 2 amino acids

A person has a cystic fibrosis phenotype. What does this mean about the protein encoded by the cystic fibrosis gene in their cells?

the protein is not functional

An alien species has 102 chromosomes in its diploid somatic cells. Its haploid gametes will have _____ chromosomes.

51

Mexican hairless dogs are hairless because of a dominant allele of a particular gene. Homozygous dominant dogs die in utero (before being born). What is the probability of two hairless dogs having a hairy puppy?

1/4

A person has cystic fibrosis. What does this mean about their alleles in the cystic fibrosis gene?

both are non-functional

Are all mutations harmful?

No, not all mutations change the amino acid sequence of the protein.




No, some mutations are beneficial.

Having two copies of every chromosome is referred to as being:

diploid

A mutation in the coding sequence of the CFTR gene does not change the amino acid sequence of the CFTR protein. This mutation is most likely to be _____.

neutral (has no effect)

A person inherits a functional cystic fibrosis allele from both parents. This person will have cystic fibrosis.

false

define homozygous

have two identical allelles

independent assortment

the principle that alleles of different genes are distributed independently of one another during meiosis

what are gametes

specialized reproductive cells that carry one copy of each chromosome (haploid).




ex: sperm= male gametes


egg=female gamete

what is meiosis

a specialized type of nuclear division that generates genetically unique haploid gametes

Haploid

having only one copy of every chromosome

mutation

A change in the nucleotide sequence of DNA.

homologous chromosomes

A pair of chromosomes that both contain the same genes.




In a diploid cell, one chromosome in the pair is inherited from the mother, the other from the father.

diploid

having two copies of every chromosome

embryo

An early stage of development reached when a zygote undergoes cell division to form a multicellular structure.

heterozygous?

having two different alleles

punnett square

A diagram used to determine probabilities of offspring having particular genotypes, given the genotypes of the parents.

recombination

An event in meiosis during which maternal and paternal chromosomes pair and physically exchange DNA segments.

zygote

a fertilized egg

A visual representation of the occurrence of phenotypes across generations is called a _____.

pedigree

A form of inheritance in which heterozygotes have a phenotype that is intermediate between homozygous dominant and homozygous recessive is:

incomplete dominance

The failure of chromosomes to separate accurately during cell division is called:

nondisjunction

How does an XX female inherit her two chromosomes?

one from mom and one from dad

X-linked traits are most typically inherited by _____ from their _____.

sons; mothers

A woman produces an egg with 24 chromosomes, including two copies of chromosome 21. If the egg is fertilized by a normal sperm, the zygote will have _____ chromosomes.

47

Which two people would have the most different Y chromosome?

a father and his daughter's biological son

A form of inheritance in which both alleles contribute equally to the phenotype is _____.

codominance

A pregnant woman has amniocentesis in order to:

examine the embryonic/fetal karyotype.

what kind of couple could have a boy with Duchenne Muscular Dystrophy (DMD)?

a male with DMD and a carrier female

The combination of alleles a person inherits (aabbcc, AabbCc, etc.) predicts a distinct phenotype. We call this type of inheritance:

polygenic

A person with 47 total chromosomes has a karyotype that can best be described as _____.

aneuploid

true or false:


A phenotype determined by an allele on the X chromosome is called an X-linked trait.

true

A mating of two people of medium height (where three genes control height): AaBbCc x AaBbCc produce _____ distinct phenotypes determined by the number of genes inherited.

seven

true or false:


Karyotype analysis can be used to detect trisomy 21 prenatally.

true

Which of the following most influences the development of a female fetus?

the absence of a Y chromosome

A trait with polygenic inheritance is influenced by:

alleles of multiple genes

A sperm with two copies of chromosome 15 is fertilized by a normal egg. The zygote will have a(n) _____ karyotype.

aneuploid

what are autosomes

the paired chromosomes present in both males and females.




all chromosomes except the X and Y chromosomes.

true or false:


A person with type B blood makes antibodies against the "B" antigen.

false

A shorter form of the allele for serotonin transporter protein has been linked to _____ in humans.

anxiety disorder

A liver cell of a person with Down syndrome has _____ chromosomes.

47

You have type B blood. Therefore you can accept blood donations from people with a(n) _____ genotype.

BB and BO

A black dog is bred with a brown dog, and all the puppies have patches of black and brown. The color coat alleles for black and brown are an example of:

codominance

A man with straight hair marries a woman with wavy hair. What is the chance that their first child will have wavy hair?

50%

An individual inheriting the genotype aaBbCc falls in the _____ foot phenotype.

five

A procedure that removes fluid surrounding the fetus to obtain and analyze fetal cells to diagnose genetic disorders.

AMNIOCENTESIS

An interaction between genes and the environment that contributes to a phenotype or trait.

MULTIFACTORIAL INHERITANCE

The failure of chromosomes to separate accurately during cell division;




in meiosis leads to aneuploid gametes.

nondisjunction

Variation in a population showing an unbroken range of phenotypes rather than discrete categories.

CONTINUOUS VARIATION

A form of inheritance in which heterozygotes have a phenotype that is intermediate between homozygous dominant and homozygous recessive.

incomplete dominance

An abnormal number of one or more chromosomes (either extra or missing copies).

ANEUPLOIDY

Sex organs: ovaries in females, testes in males.

GONADS

A trait whose phenotype is determined by the interaction among alleles of more than one gene.

POLYGENIC TRAITS

Carrying an extra copy of chromosome 21; also known as Down syndrome.

TRISOMY 21

A phenotype determined by an allele on an X chromosome.

x-linked traits

Comparing sequences on the Y chromosome to examine paternity and paternal ancestry.

Y-CHROMOSOME ANALYSIS

Mendel's Law of Segregation

for any diploid organism, the 2 alleles of each gene segregate separately into gametes.




---every gamete receives only one of the two alleles and the specific allele that any one gamete receives is random

Mendel's Law of Independent Assortment

two alleles of any given gene segregate independently from any two alleles of a second gene




-bc of this, offspring can display any combo of the diff traits rather than inheriting the traits together

Mexican hairless dogs are hairless because of a dominant allele of a particular gene. Homozygous dogs die in utero (before being born). What is the probability of one hairless dog having a hairy puppy?

0%

true or false:




A person inherits a functional cystic fibrosis allele from both parents. This person will have cystic fibrosis.

false

If two genes are located next to one another on the same chromosome, can you use the Punnett square to assess inheritance of the two genes?

no

Mexican hairless dogs are hairless because of a dominant allele of a particular gene. Homozygous dominant dogs die in utero (before being born). What is the probability of two hairless dogs having a hairless puppy?

2/3

Gamete:




How many chromosomes in one gamete




How many alleles of each gene present

23; 1