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GENETICS
SLHS UNIT 4 GENETICS
| Question | Answer |
|---|---|
| the father of genetics | Gregor Mendel |
| discovered the shape of DNA | Watson & Crick |
| a characteristic that is determined by genes | trait |
| the passing of traits from parents to offspring | heredity |
| part of the DNA that is used to make a protien | gene |
| different versions of a gene | allele |
| an organism's inherited physical appearance | phenotype |
| an organism's inherited combination of genes | genotype |
| the mathematical chance that an event will occur | probability |
| differences amongst organisms | variation |
| a molecule that determines the traits a living thing inherits and needs to survive | DNA |
| a copy of DNA used to make proteins | RNA |
| an organelle that makes proteins | ribosomes |
| the organelle that stores and protects DNA | nucleus |
| coiled structure of DNA during cell division | chromosome |
| a molecule used to build and repair cells and regulate chemical reactions in living things | protein |
| cell division that results in cells with half the original number of chromosomes | meiosis |
| a tool used to predict the genotypes and phenotypes of the offspring of a mating pair | punnett Square |
| the process of putting the genes from one organism into the DNA of another organism | genetic engineering |
| an organism with two different alleles for a trait | heterozygous |
| the scientific study of heredity | genetics |
| graphic representation of genetic inheritance used by geneticists to map genetic traits | pedigree |
| In humans, the 23rd pair of chromosomes; determine the sex of an individual and carry sex-linked characteristics | sex chromosome |
| traits controlled by genes located on sex chromosomes | sex-linked trait |
| chart of metaphase chromosome pairs arranged according to length and location of the centromere; used to pinpoint unusual chromosome numbers in cells | karyotype |
| genetically identical copies of an organism or gene | clone |
| insertion of normal genes into human cells to correct genetic disorders | gene therapy |
| an individual heterozygous for a specific trait | carrier |
| a trait that is always xpressed when present | dominant trait |
| a trait that is only expressed if a dominant allele is not present. | recessive trait |
| percent chance of having an albino child from a cross with 2 people who are both heterozygous for albinism. | 25 percent |
| an organism that has two identical alleles for a trait | homozygous |
| genotype of an organism that is homozygous dominant for the tongue rolling trait | TT |
| genotype of an organism that is homozygous recessive for the tongue rolling trait | tt |
| genotype of an organism that is heterozygous for the tongue rolling trait | Tt |
| karyotype description for a male with Down's Syndrome | 47XY + 21 |
| karyotype description for a female with Trisomy 18 | 47XX + 18 |
| shape on a pedigree that represents a male | square |
| shape on a pedigree that represents a female | circle |
| Chromosomal abnormality that occurs when one chromosome is attached to another and can not be removed | translocation |
| chromosomal abnormality that occurs when a cell divides in meiosis and two of the same chromosome go into one sex cell | non-disjunction |