Heredity Flash cards

1
Q

Allele

A

different forms of a gene.

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2
Q

Genotype

A

the combination of genes for one or morevtraits.

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3
Q

Phenotype

A

an organisms apperance or other detectable.characteristic

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4
Q

Homozygous

A

having identical pairs of genes for any given pair of hereditary characteristics.

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5
Q

Heterozygous

A

having dissimilar pairs of genes for any hereditary characteristic.

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6
Q

Dominant trait

A

In genetics, a trait that will appear in the offspring if one of the parents contributes it.

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7
Q

Recessive Trait

A

In genetics, a trait that must be contributed by both parents in order to appear in the offspring.

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8
Q

`Mitosis

A

the usual method of cell division, characterized typically by the resolving of the chromatin of the nucleus into a threadlike form, which condenses into chromosomes, each of which separates longitudinally into two parts, one part of each chromosome being retained in each of two new cells resulting from the original cell.

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9
Q

Meiosis

A

part of the process of gamete formation, consisting of chromosome conjugation and two cell divisions

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10
Q

identical twins

A

one of a pair of twins who develop from a single fertilized ovum and therefore have the same genotype, are of the same sex, and usually resemble each other closely.

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11
Q

Fraternal twins

A

one of a pair of twins, not necessarily resembling each other, or of the same sex, that develop from two separately fertilized ova.

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12
Q

Sex-linked disorder

A

a genetic disorder that is found on the x chromosome.

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13
Q

Chromosome

A

any of several threadlike bodies, consisting of chromatin, that carry the genes in a linear order: the human species has 23 pairs

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14
Q

Gene

A

the basic physical unit of heredity; a linear sequence of nucleotides along a segment of DNA that provides the coded instructions for synthesis of RNA, which, when translated into protein, leads to the expression of hereditary character.

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15
Q

DNA

A

Genetics. deoxyribonucleic acid: an extremely long macromolecule that is the main component of chromosomes and is the material that transfers genetic characteristics in all life forms, constructed of two nucleotide strands coiled around each other in a ladderlike arrangement with the sidepieces composed of alternating phosphate and deoxyribose units and the rungs composed of the purine and pyrimidine bases adenine, guanine, cytosine, and thymine: the genetic information of DNA is encoded in the sequence of the bases and is transcribed as the strands unwind and replicate.
Compare base pair, gene, genetic code, RNA.

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16
Q

DNA replication

A

DNA replication is the process of producing two identical replicas from one original DNA molecule. This biological process occurs in all living organisms and is the basis for biological inheritance.

17
Q

Double helix

A

the spiral arrangement of the two complementary strands of DNA.

18
Q

Chargaff’s rule

A

Found that the amount of Adenine equals the amount of thymine

19
Q

Mutation

A

a sudden departure from the parent type in one or more heritable characteristics, caused by a change in a gene or a chromosome.

20
Q

Deletion

A

a type of chromosomal aberration in which a segment of the chromosome is removed or lost.

21
Q

Insertion

A

addition of one or more nucleotide base pairs into a DNA sequence. This can often happen in microsatellite regions due to the DNA polymerase slipping.

22
Q

Substitution

A

s the evolutionary substitution of one base for another in an exon of a gene coding for a protein, such that the produced amino acid sequence is not modified.