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genetic terms

Terms

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Polymerase
any enzyme that catalyzes the formation of DNA or RNA from deoxyribonucleotides or ribonucleotides
Autosome
a nuclear chromosome other than the X- and Y-chromosomes.
Gamete
a haploid cell.gel electrophoresis the process by which nucleic acids (DNA or RNA) or proteins are separated by size according to movement of the charged molecules in an electrical field
Recessive
A genetic disorder that appears only in patients who have received two copies of a mutant gene, one from each parent
Crossovers
the exchange of genetic material between two paired chromosome during meiosis.
Clone
genetically engineered replicas of DNA sequences
Ribosomal protein
one of the ribonucleoprotein particles that are the sites of translation.
Mutation
A permanent structural alteration in DNA.
Genotype
The genetic identity of an individual that does not show as outward characteristics
Genome
All the DNA contained in an organism or a cell, which includes both the chromosomes within the nucleus and the DNA in mitochondria
Prognosis
prediction of the course and probable outcome of a disease
Cell
The basic unit of any living organism
Deletion
the loss of a segment of the genetic material from a chromosome
Imprinting
a chemical modification of a gene allele which can be used to identify maternal or paternal origin of chromosome
Cytogenetics
the study of chromosomes.
Enzyme
A protein that encourages a biochemical reaction, usually speeding it up
Sickle cell anemia
an hereditary, chronic form of hemolytic anemia characterized by breakdown of the red blood cells; red blood cells undergo a reversible alteration in shape when the oxygen tension of the plasma falls slightly and a sickle-like shape forms
Phenotype
observable characteristics of an organism produced by the organism's genotype interacting with the environment
Chromosome
One of the threadlike "packages" of genes and other DNA in the nucleus of a cell.
Bacteria
A single-celled organism that can be found throughout nature and can be beneficial or pathogenic.
Human Genome Project
An international research project to map each human gene and to completely sequence human DNA
Dominant
A gene that almost always results in a specific physical characteristic, for example, a disease, even though the patient's genome possesses only one copy
Disease
any deviation from the normal structure or function of any part, organ, or system of the body that is manifested by a characteristic set of symptoms and signs whose pathology and prognosis may be known or unknown.
Linkage
the greater association in inheritance of two or more nonallelic genes than is to be expected from independent assortment; genes are linked because they reside on the same chromosome.
Genetic map
a chromosome map of a species that shows the position of its known genes and/or markers relative to each other

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