Genetics Ch.1-4

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Phenotype

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76 Terms

1

Phenotype

Observable Characteristic

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2

Alleles

Alternate forms of a gene

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3

Independent Assortment

alleles of one gene separate into gametes randomly with respect to alleles of other genes

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4

Gamete

Reproductive cells containing only one copy of each gene

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5

Gene

The heritable entity that determines a trait

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Segregation

The separation of the two alleles of a gene into different gametes

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Heterozygote

An individual with two different alleles of a gene

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8

Dominant

The allele expressed in the phenotype of the heterozygote

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9

F1

Offspring of the P generation

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10

Testcross

The cross an individual of ambiguous genotype with a homozygous recessive individual

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11

Genotype

The alleles an individual has

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12

Recessive

The allele that does not contribute to the phenotype of the heterozygote

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Dihybrid Cross

A cross between individuals both heterozygous for two genes

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14

Homozygote

Having two identical alleles of a given gene

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15

Epistasis

The alleles of one gene mask the effects of alleles of another gene

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Modifier Genes

Genes who alleles alter phenotypes produced by the action of other genes

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Conditional lethal

A genotype that is lethal in some situations but viable in others (eg. high temp)

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Permissive conditon

Environmental condition that allows conditional lethals to live

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Reduced penetrance

Less than 100% of the individuals possessing a particular genotype express it in their phenotype

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Complex trait

A trait produced by the interaction of alleles of multiple genes and often also the environment

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Incomplete dominance

The heterozygote resembles neither homozygote

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Codominance

Both parental phenotypes are expressed in the F1 hybrids

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Mutation

A heritable change in a gene

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Pleiotropy

One gene affects more than one trait

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Variable expressivity

Individuals with the same genotype have related phenotypes that vary in intensity

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Meiosis

One diploid cell gives rise to four haploid cells

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Gametes

Haploid germ cells that unite at fertilization

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Karyotype

The array of chromosomes in a given cell

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Mitosis

One diploid cell gives rise to two diploid cells

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Interphase

The part of the cell cycle during which the chromosomes are not visible

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Synapsis

Pairing of homologous chromosomes

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Sex Chromsomes

X and Y

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Cytokinesis

Division of the cytoplasm

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Anaphase

The time during mitosis when sister chromatids seperate

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Chromatid

One of the two identical halves of a replicated chromosome

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36

Autosomes

Chromosomes that do not differ between the sexes

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Centromeres

The sites of the closest connections between sister chromatids

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Centrosomes

Microtubule organizing centers at the spindle points

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SRY

Y-linked gene that determines maleness

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Dosage compensation

Processes that equalize the dosage of X-linked gene products in the somatic cells of males and females

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Sex-linked

The inheritance pattern of genes on X chromosome

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Hemizygous

Describe genes present in only one copy such as those on the X in males

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Pseudoautosomal regions (PAR1/2)

The tips of X and Y chromosomes

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Nondisjunction

Failure of homolog separation in meiosis I or chromatid separation in meiosis II

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X-Chromosome inactivation

In XX cells, most genes a random X chromosome are turned off

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Klinefelter syndrome

XXY Males

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Turner syndrome

XO females

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Oogonia

Cells in the ovary that undergo mitosis

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Oocytes

Cells in the ovary that undergo meiosis

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Spermatid

Haploid cell at the end of meiosis II that will become a sperm

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Spermatocytes

Cells in the testes that undergo meiosis to create spermatid

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Epistatic

gene that is masking other gene

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Hypostatic

gene that is being masked

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Additive

Four distinct F2 phenotypes, 9:3:3:1

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Recessive Epistasis

Homozygous recessive allele of one gene masks both alleles, 9:3:4

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Reciprocal recessive epistasis

When homozygous recessive of either gene masks the dominant allele of the other gene, 9:7

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Dominant Epistasis 1

Dominant allele of one gene hides effects of both alleles of the other gene, 12:3:1

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Redundancy

Only one Dominant allele of either two genes is necessary to produce phenotype, 15:1

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Complementation

Mutations in two different genes. For example aaBB x AAbb, both have no hearing, the child will have hearing because it is heterozygous

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Noncomplementation

Mutations in the same gene. For example AAbb x AAbb, both have no hearing, the child will not have hearing.

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Penetrance

How many members of a population with a particular genotype, show the expected phenotype

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Complete Penetrance

Mendels Studies

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Incomplete Penetrance

75% percent of the people with mutant allele get the disease

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Expressivity

The degree or intensity a genotype is expressed in phenotype

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Modifier Genes

Alter the phenotype produced by alleles of other genes

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Permissive

Range of temps that allele is functional

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Restrictive

Range of temps that allele is not functional

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Conditional lethal

allele is lethal under certain conditions

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Discontinuous Trait

Two distinct phenotypes, smooth/wrinkled

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Continuous Trait

Trait that has a variation of phenotypes, height/weight

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G1

Growing and preparation for S phase

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S phase

DNA synthesis and chromosome duplication

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G2

Growth and preparation for mitosis

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Reductional vs Equational Division

reductional division reduces the number of chromosomes in a cell, while equational division does not

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Autosome

Chromosome not involved in sex determination

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Sex Chromosome

Chromosome that determine sex of an organism

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