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Unit 4 Vocab

Total questions: 39

Worksheet time: 20mins

Name
Class
Date
1.

Define the following: Gamete

a)

A diploid cell that is used in fertilization and reproduction

b)

A diploid body cell that reproduces via mitosis

c)

A haploid cell that is used in fertilization and reproduction

d)

A diploid body cell that reproduces via mitosis

2.

Define the following: Homologous Chromosomes

a)

Matching chromosomes from mom and dad

b)

Cells that have 2 sets of chromosomes

c)

Chromosomes that have been mutated or damaged

d)

Chromosomes that have not been copied yet

3.

Define the following: Diploid

a)

Cells with 1 set of DNA

b)

Cells with 2 sets of DNA

c)

Cells with specialized functions

d)

Single-celled organisms

4.

Define the following: Haploid

a)

Cells with 1 set of DNA

b)

Cells with 2 sets of DNA

c)

Cells with specialized functions

d)

Multi-celled organisms

5.

Define the following: Cross

a)

When a virus or illness passes from one organism to another

b)

When cells exchange genetic information

c)

A mating of 2 organisms

d)

When 2 different species produce an offspring

6.

Define the following: Gene

a)

A folded/condensed unit of DNA

b)

sections of DNA that provide instructions for making protein

c)

DNA monomer made of a phosphate, nitrogen base, and deoxyribose

d)

A 2 nucleotide sequence that codes for a certain amino acid

7.

Define the following: Genotype

a)

the actual alleles inherited

b)

the physical presentation of alleles

c)

A section of DNA that codes for a specific protein

d)

A protein that is produced via transcription and translation

8.

Define the following: Phenotype

a)

the allele inherited from your mother

b)

the actual alleles inherited

c)

the physical characteristics or traits of an organism

d)

the allele inherited from your father

9.

Define the following: Allele

a)

When 2 traits assort independently

b)

The process of crossing 2 organisms to produce offspring

c)

The physical trait that is expressed based on an organism's genetics

d)

A version of a gene

10.

Define the following: Homozygous

a)

Chromosomes that pair: 1 from mom, 1 from dad

b)

An individual inheriting 2 copies of the same allele

c)

An individual inheriting 2 different alleles

d)

Chromosomes that are joined at the centromere

11.

Define the following: Heterozugous

a)

Chromosomes that pair: 1 from mom, 1 from dad

b)

An individual inheriting 2 copies of the same allele

c)

An individual inheriting 2 different alleles

d)

Chromosomes that are joined at the centromere

12.

Define the following: Dominant

a)

Overshadows the other allele in the heterozygous state

b)

An offspring that is more fit to survive than others

c)

An allele that is only expressed in homozygous individuals

d)

An offspring that inherits traits directly from parents

13.

Define the following: Recessive

a)

An allele that will cause it's trait to always be expressed

b)

An offspring that is less fit to survive than others

c)

An allele that is only expressed when a dominant allele is not present

d)

An offspring that inherits traits its parents didn't have

14.

Define the following: Punnett square

a)

A diagram that shows the path information takes from DNA to protein

b)

A diagram that shows the probability of inheriting traits from parents with certain genes

c)

A diagram to track energy flow from parent to offspring

d)

A diagram to keep track of all of the genes expressed by an offspring

15.

Define the following: Dihybrid cross

a)

Finding probabilities of inheritance based on one gene

b)

Finding probabilities of inheritance based on 2 genes

c)

Crossing one species at a time

d)

Crossing 2 species at a time

16.

Define the following: Law of Dominance

a)

Mendel's Law saying the a dominant allele will be expressed over a recessive allele

b)

Mendel's Law saying that the most powerful offspring will survive

c)

Mendel's Law saying that only the best traits will show up in offspring

d)

Mendel's Law saying that only significant alleles will be passed on

17.

Define the following: Law of Segregation

a)

Mendel's Law saying that offspring with different traits will stay apart

b)

Mendel's Law saying that gametes will only have one chromosome from each homologous pair

c)

Mendel's Law saying that cells will split apart when they have all the genes they need

d)

Mendel's Law saying that offspring will only inherit traits their parents express

18.

Define the following: Law of Independent Assortment

a)

Mendel's Law saying that offspring will form hierarchies based on strength

b)

Mendel's Law saying that phenotypes are independent from genotypes

c)

Mendel's Law saying that the inheritance of one trait will not effect the inheritance of other traits

d)

Mendel's Law saying that parents don't decide which traits are passed onto offspring

19.

Define the following: Autosome

a)

Chromosomes 45-46 in a human, has an effect on their gender

b)

Chromosomes 1-44 in a human, does not effect their gender

c)

A disease that caused a human's immune system to attack their own body

d)

A section of a chromosome that controls the autopilot function of a cell

20.

Define the following: Sex Chromosomes

a)

Chromosomes 45-46 in a human, has an effect on their gender

b)

Chromosomes 1-44 in a human, does not effect their gender

c)

A disease that caused a human's immune system to attack their own body

d)

A section of a chromosome that controls the autopilot function of a cell

21.

Define the following: Chromosome

a)

The pinched region that separates genetic material into a short arm and a long arm

b)

The repeating DNA that protect the genetic information from damage

c)

Condensed genetic material

d)

A cylindrical organelle that developments spindle fibers for cell division

22.

Define the following: Codominance

a)

When the heterozygous genotype results in a phenotype where the two alleles are blended together

b)

When several genes influence a trait

c)

More than 2 versions of a gene (more than just a "dominant" and a "recessive")

d)

When the heterozygous genotype results in a phenotype where both alleles are fully and separately expressed

23.

Define the following: Incomplete Dominance

a)

When the heterozygous genotype results in a phenotype where the two alleles are blended together

b)

When several genes influence a trait

c)

More than 2 versions of a gene (more than just a "dominant" and a "recessive")

d)

When the heterozygous genotype results in a phenotype where both alleles are fully and separately expressed

24.

Define the following: Polygenic Inheritance

a)

When the heterozygous genotype results in a phenotype where the two alleles are blended together

b)

When several genes influence a trait

c)

More than 2 versions of a gene (more than just a "dominant" and a "recessive")

d)

When the heterozygous genotype results in a phenotype where both alleles are fully and separately expressed

25.

Define the following: Multiple Alleles

a)

When the heterozygous genotype results in a phenotype where the two alleles are blended together

b)

When several genes influence a trait

c)

More than 2 versions of a gene (more than just a "dominant" and a "recessive")

d)

When the heterozygous genotype results in a phenotype where both alleles are fully and separately expressed

26.

Define the following: Sex-Linked

a)

Genes that are likely inherited together due to the physical proximity

b)

When several genes influence a trait

c)

When one gene overshadows the other

d)

Genes that travel on the X chromosome and are not on the Y chromosome

27.

Define the following: Linked Genes

a)

Genes that are likely inherited together due to the physical proximity

b)

When several genes influence a trait

c)

Genes that are always inherited together

d)

Genes that travel on the X chromosome and are not on the Y chromosome

28.

Define the following: Epistasis

a)

When genes stop expressing their traits

b)

When several genes influence a trait

c)

When both genes blend together to make a new phenotype

d)

When one gene overshadows another

29.

Define the following: Karyotype

a)

A diagram that shows the amino acids that make up a stand of DNA

b)

A diagram that shows homologous pairs of chromosomes

c)

A diagram that shows the probability of potential offspring

d)

A diagram showing the process of meiosis

30.

Define the following: Carrier

a)

A person that has the gene for a trait or disease but doesn't show it

b)

The transfer of a gene from the DNA of one organism into another organism to produce offspring with desired trait

c)

A person with homozygous gene that does not have a trait or disease

31.

Define the following: Mutagen

a)

An alteration in the nucleotide sequence

b)

Chemicals or physical effects that can cause DNA mutations

c)

A normal cellular process that mutes your genes

d)

An alteration to your gene that causes it to work more efficiently

32.

Define the following: Mutation

a)

Any change in an organism's physical appearance

b)

Any change in an organism's ability to maintain homeostasis

c)

Any change in DNA (the order of nucleotide bases/letters)

d)

Any change in the the climate outside

33.

Define the following: Gene Mutation

a)

This happen during DNA replication; A change to the original DNA sequence

b)

This happens during meiosis; Changes the number or location of genes

34.

Define the following: Chromosome Mutation

a)

This happen during DNA replication; A change to the original DNA sequence

b)

This happens during meiosis; Changes the number or location of genes

35.

Define the following: Point Mutation

a)

The insertion of a nucleotide

ATTACC -> ACTTACC

b)

The substitution of one nucleotide for another

ATTACC -> AATACC

c)

The deletion of a nucleotide

ATTACC -> ATACC

36.

Define the following: Frameshift Mutation (select all that apply)

a)

The insertion of a nucleotide

ATTACC -> ACTTACC

b)

The substitution of one nucleotide for another

ATTACC -> AATACC

c)

The deletion of a nucleotide

ATTACC -> ATACC

37.

Define the following: Duplication

a)

Changes the size of chromosomes and results in multiple copies of a single gene

b)

Pieces of non-homolgous chromosomes exchange segments (during crossing over)

c)

Chromosomes do not separate correctly during anaphase, resulting in 1 or 3 chromosomes rather than 2 per cell

38.

Define the following: Nondisjunction

a)

Changes the size of chromosomes and results in multiple copies of a single gene

b)

Pieces of non-homolgous chromosomes exchange segments (during crossing over)

c)

Chromosomes do not separate correctly during anaphase, resulting in 1 or 3 chromosomes rather than 2 per cell

39.

Define the following: Translocation

a)

Changes the size of chromosomes and results in multiple copies of a single gene

b)

Pieces of non-homolgous chromosomes exchange segments (during crossing over)

c)

Chromosomes do not separate correctly during anaphase, resulting in 1 or 3 chromosomes rather than 2 per cell