Basic physical and functional unit of heredity, made up of DNA
Alleles
Variant form of a gene
Homozygous
2 alleles are similar
Heterozygous
2 alleles are different
Phenotype
Expression of the code or the genotype
Genotype
Genetic code of individual
PunnettSquare
Squarediagram used to predict the genotypes of a particular cross or breeding experiments
Reginald C. Punnett - based on the name of the punnett square
Monohybrid
Cross happening in the F1 generation offspring of parents differing in one trait only
Dihybrid
Cross happening to F1 generation offspring differing in two traits
GregorMendel
Father of ModernGenetics, Austrian monk and teacher who experimented with garden peas
GardenPeas
Contains pollen and pistils, producing through sexual reproduction, completeflowers with both female and male parts
Incomplete Dominance
Two alleles blend their characteristics with a trait, neither one is dominant
Codominance
Existing in both, some alleles are present but not blended, neither allele is dominant or recessive
Nucleotide (Base Pairing)
Building blocks of DNA, connected through hydrogen bonds
4 Main Nucleotides
Thymine
Adenine
Cytosine
Guanine
DNA consists of 300 to 1 millionnucleotides
Gene
Basic unit of heredity, where traits can be found, needed to produce offspring and transmitted to next generation
DNA (Deoxyribonucleic Acid)
Long chain of nucleotides, genetic material that contains information about a person, makes up chromosomes
RNA (Ribonucleic Acid)
Carrying genetic information, single stranded sugar phosphate with single set of nucleotides (Uracil, Adenine, Cytosine, Guanine)
Histones
Basic proteins found in eukaryotic cells, wrap DNA, proteins that DNA is tightly coiled around
Chromatin
Coil genetic material, package the long DNA nucleotide into more compact and dense structures
Chromatid
One of the two identical halves of a duplicated chromosome, also known as sister chromatids, connected by the centromere
Homologous Chromosomes
Two pieces of DNA within a diploid organism which carry the same genes, one from each parental source
Chromosomes
Ribbon-like structure of DNA, most compact, threadlike structure of nucleic acids carrying genetic information
We have 23 pairs of chromosomes
Genome
Full set of DNA made of chromosomes
We need to compress DNA to form chromosomes due to celldivision, and all chromosomes will be duplicated during interphase
We can count chromosomes by looking at the centromere, not all chromosomes are X-shaped, DNA in prokaryoticcells are usually circular
AutosomalChromosomes
1st and 22ndchromosomes, have genes related to eye color, height, hair structure, and traits
SexChromosomes
The 23rd chromosome, have genes that distinguish biological sex (xy=boy, xx=girl)
The sex will depend on the father, 50-51%probability of having a boy or girl depending on whether the sperm is x or y
Karyotype
Picture or image of all of a person's chromosomes, used by doctors to detect abnormalities
Things to consider in Karyotyping
Number of chromosomes, sizes of chromosomes, shapes or structure of chromosomes
Trisomy21 (DownSyndrome)
Extrafull or partialcopy of chromosome 21, causes mild to moderate cognitiveimpairment, language delay, and memoryissues
Common features of Trisomy21
Flattened face, small head, short neck, protruding tongue, upward slanting eye lids, short fingers and small hands and feet, short height
45X (TurnerSyndrome)
45 chromosomes instead of 46, partially or completely missing chromosomes, only happens in females
Signs of 45 X
Wide or weblike neck, low set ears, broad chest with widely spaced nipples, swelling of hands and feet, slowed growth, failure to begin sexual changes in puberty, early end to menstrual cycles