Glencoe Biology Chapter 11 Test

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59 Terms

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True

True or False: Most diseases and disorders are recessive disorders, which are rare, but are mostly common in certain ethnic or small groups..

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Homozygous Recessive

Fill In The Blank: In order for a recessive disorder to be expressed, it must be __________________________ ___________________.

<p>Fill In The Blank: In order for a recessive disorder to be expressed, it must be __________________________ ___________________.</p>
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Heterozygotes

Heterozygous individuals; only carry the trait - called carriers

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Cystic Fibrosis

(Recessive)Most common among Caucasians; most often lethal; mucous build-up in lungs and digestive system; poor digestion & breathing; drugs & therapy to help

<p>(Recessive)Most common among Caucasians; most often lethal; mucous build-up in lungs and digestive system; poor digestion &amp; breathing; drugs &amp; therapy to help</p>
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Cystic Fibrosis

(Recessive)Mucous build-up in the lungs and digestive system; causes poor digestion and breathing; drugs and therapy can help this

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Albanism

(Recessive)Can occur in any race (humans & animals); absence of the skin pigment, called melanin; white hair, very pale skin, and pink pupils; the eyes may be blue or pink; different types; skin causes severe problems

<p>(Recessive)Can occur in any race (humans &amp; animals); absence of the skin pigment, called melanin; white hair, very pale skin, and pink pupils; the eyes may be blue or pink; different types; skin causes severe problems</p>
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Melanin

Absence of a skin pigment

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Albanism

(Recessive)Absence of the skin pigment, called melanin; can cause white hair, very pale skin, and pink pupils (eyes may be blue or pink)

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Tay-Sachs Disease

(Recessive)Most common in Penn-Dutch in US & Jewish people with European ancestry; gene is on chromosome 15; a CNS problem; build-up of lipids in the cells due to a lack of enzymes; red spot on back of eye; blindness, loss of movement, and mental deterioration; has no treatment

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Tay-Sachs Disease

(Recessive)Build-up of lipids in the cells due to a lack of enzymes, causing a red spot on back of the eye; can lead to blindness, loss of movement, and mental deterioration; has no treatment

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PKU

(Recessive)Common among Swedish or Norwegian ancestry; caused by a missing enzyme that is need to change phenylalanine (amino acid) to tyrosine; Phenylalanine builds up in the CNS; leads to mental retardation; noticed when a baby drinks milk

<p>(Recessive)Common among Swedish or Norwegian ancestry; caused by a missing enzyme that is need to change phenylalanine (amino acid) to tyrosine; Phenylalanine builds up in the CNS; leads to mental retardation; noticed when a baby drinks milk</p>
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PKU

(Recessive)Caused by a missing enzyme that is needed to change phenylalanine (amino acid) to tyrosine; the phenylalanine builds up in the CNS; leads to mental retardation, noticed when a baby drinks milk.

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True

True or False: Mental retardation from PKU can be prevented if the baby is treated with special diet the first 7-10 days of life

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Phenylalanine

An kind of amino acid

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False (They tend to be recessive)

True or False: Disorders and diseases tend to be dominant.

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One

How many dominant alleles are needed in order for a Dominant Genetic Disorder to be expressed?

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Huntington's Disease

(Dominant)Rare, hereditary; degeneration of the nervous system; uncontrollable jerky movement of head & limbs; mental deterioration; onset 30-50

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Huntington's Disease

(Dominant)Degeneration of the nervous system, causing uncontrollable jerky movement of the head or limbs; mental deterioration

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Achondroplasia

(Dominant)Common form of dwarfism; disorder of bone growth; short limbs; height not exceeding 4 ft; 85% are result of a new mutation

<p>(Dominant)Common form of dwarfism; disorder of bone growth; short limbs; height not exceeding 4 ft; 85% are result of a new mutation</p>
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Achondroplasia

Disorder of bone growth, causing short limbs and a height not exceeding 4 feet; 85% are a result of a new mutation

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True

True or False: Not all inheritance patterns follow Mendel's Rules.

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Incomplete Dominance

Some traits have more than one dominant for a trait; traits are inherited incompletely; the phenotype of offspring between 2 homo dominant parents is intermediate (appearance of a third phenotype); neither allele is completely dominant - both produce traits; the alleles combine to give a new trait; ex- R-red + R'R'(white) = RR'(pink)

<p>Some traits have more than one dominant for a trait; traits are inherited incompletely; the phenotype of offspring between 2 homo dominant parents is intermediate (appearance of a third phenotype); neither allele is completely dominant - both produce traits; the alleles combine to give a new trait; ex- R-red + R'R'(white) = RR'(pink)</p>
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Codominance

Also occurs when there is a trait with more than one dominant form; a combination of two forms of dominance; ex- if both parents are homo dominant, both phenotype will show in offspring; the traits are expressed equally; ex- C-curly hair, S- straight hair, CC + SS=CS offspring with wavy hair (some straight, some curly sections)

<p>Also occurs when there is a trait with more than one dominant form; a combination of two forms of dominance; ex- if both parents are homo dominant, both phenotype will show in offspring; the traits are expressed equally; ex- C-curly hair, S- straight hair, CC + SS=CS offspring with wavy hair (some straight, some curly sections)</p>
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True

True or False: To differentiate from Incomplete Dominance, different letters are represented as the dominant traits (no slash).

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True

True or False: Sickle Cell Anemia is an example of codominance in humans.

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Sickle Cell Anemia

Blood disorder; affects 1 in 12 African Americans; malfunctIion (caused by a missing amino acid in the hemoglobin) of the red blood cells; clogging of the blood vessels; poor circulation; low rbc count (anemia); can cause stroke

<p>Blood disorder; affects 1 in 12 African Americans; malfunctIion (caused by a missing amino acid in the hemoglobin) of the red blood cells; clogging of the blood vessels; poor circulation; low rbc count (anemia); can cause stroke</p>
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True

True or False: Individuals who are heterozygous for Sickle Cell Anemia produce both normal and sickled cells (codominance) and have enough normal hemoglobin to prevent serious effects.

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True

True or False: Multiple Phenotypes are determined by greater than 2 alleles, such as blood groups in humans

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I^A, I^B, & i

What are the 3 alleles that are involved in blood groups in humans?

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I^A & I^B

Which 2 alleles are codominant with each other in blood groups?

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Type A

I^A I^A

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Type B

I^B I^B

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Type AB

I^A I^B

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Type O

i i

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C'

Fill In The Blank: Coat color: C-black, c-brown, C'-white spotting, c'-white

CC'-black with white spotting

Cc-black and brown for mixture

C'c-brown with white spotting

_____c'-white

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40

Fill In The Blank: Different combinations make over _______ different coat colors in rabbits.

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Autosomes

The first 22 pairs of chromosomes

<p>The first 22 pairs of chromosomes</p>
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Sex Chromosomes

The 23rd pair of chromosomes; different in males and females; control the inheritance of sex characteristics; thousands of other traits

<p>The 23rd pair of chromosomes; different in males and females; control the inheritance of sex characteristics; thousands of other traits</p>
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XX

Female

<p>Female</p>
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XY

Male

<p>Male</p>
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Sex-Linked Trait(s)

Controlled by genes on sex chromosomes; most are on the X allele in humans

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Sex-Linked Trait(s)

If a trait is X-linked, a male will pass it to a daughter, not a son. The daughter can pass it on (50/50 chance) to her children. If a son inherits it, he will show the recessive phenotype because he will not receive an X-dominant allele from his father to mask it.

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Red-Green Color Blindness

Red & green cannot be distinguished; men inherit the recessive allele on their X chromosome; rare in female; hemophilia (disease characterized by the inability to clot blood)

<p>Red &amp; green cannot be distinguished; men inherit the recessive allele on their X chromosome; rare in female; hemophilia (disease characterized by the inability to clot blood)</p>
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Hemophilia

Disease characterized by the inability to clot blood due to a lack of the clotting enzyme Factor VIII; passed on from mother to son

<p>Disease characterized by the inability to clot blood due to a lack of the clotting enzyme Factor VIII; passed on from mother to son</p>
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Polygenic Trait(s)

Traits controlled by more than one pair of genes; 3-5 pairs; include human eye, hair color, skin color, height, body shape, fingerprint patterns; skin color is controlled by three genes: A, B, C

<p>Traits controlled by more than one pair of genes; 3-5 pairs; include human eye, hair color, skin color, height, body shape, fingerprint patterns; skin color is controlled by three genes: A, B, C</p>
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True

True or False: Human eye color, hair color, skin color, height, body shape, & fingerprint patterns are polygenic traits.

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False(Capitals are not dominant over lowercase)

True or False: For polygenic traits, capitals are dominant over lowercase.

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AABBCC

Darkest shade for skin tone

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aabbcc

Lightest shade for skin tone

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AaBbCc

Intermediate shade for skin tone

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Genetic Makeup

What factor determines potential to develop and function?

<p>What factor determines potential to develop and function?</p>
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Internal Environment

Age, gender, hormones, the existence of an infection, etc.

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External Environment

Temperature, nutrition, light, chemicals, infectious agents, etc.

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Pedigree(s)

Shows family history of a particular inherited trait; diagram uses symbols for the data

<p>Shows family history of a particular inherited trait; diagram uses symbols for the data</p>
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Pedigree Symbols

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Pedigree (Abortion or Stillbirth)

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Pedigree Graph Rules

1. Always label the homo recessive FIRST

2. Give every other individual one capital letter

3. Work backwards from a homo recessive

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Heterozygous

Is #4 a Homozygous or a Heterozygous

<p>Is #4 a Homozygous or a Heterozygous</p>
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Heterozygous

Is #7 a Homozygous or a Heterozygous

<p>Is #7 a Homozygous or a Heterozygous</p>