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as92022 L1 basics
genetic terms required for understanding
| Term | Definition |
|---|---|
| Genome | The complete set of genetic material (DNA) in an organism |
| Karyotype | organized profile of a person's chromosomes/genome |
| Homologous pair of chromosomes | two chromosomes have the same genes in the same location. Alleles for the genes maybe different |
| Allele | alternate version of a gene, due to a change in the DNA base sequence. |
| DNA | A double helix shaped molecule that carries the genetic instructions for an organisms development and function, via the base code A,T,C,G. |
| Nucleotide | A building block of DNA, consisting of a sugar, phosphate group and a nitrogenous base (A,T,C,G) . |
| Complementary base pair rule | A rule that describes how nitrogen bases in DNA pair up: Adenine (A) always pairs with Thymine (T), and Guanine (G) always pairs with Cytosine (C). |
| Chromosomes | Length of DNA containing many genes, stored in the nucleus of cells |
| Gene | Sequence of DNA bases that code for a protein/trait |
| Sexual reproduction | the process where genetic material from two parents combines to form a new, unique offspring |
| Fertilisation | Genetically unique egg and sperm fuse to become a genetically unique zygote. |
| Zygote | Genetically unique first cell formed via fertilization. |
| inheritance | the process by which genetic information is passed on from parent to child. |
| phenotype | Physical expression of the genotype (and its interactions with the environment) |
| genotype | The two alleles inherited for a trait |