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Genetics
is the scientific study of genes
and heredity—of how certain qualities or
traits are passed from parents to offspring
because of changes in DNA sequence.
Mendel's
pea
plant experiments conducted
between 1856 and 1863 established many
of the rules of heredity, now referred to as
the laws of Mendelian inheritance.
Mendel worked with seven characteristics of pea plants:
plant height
, pod shape and color, seed shape and color, and
flower position and color.
An
allele
is one of a pair of genes that
appear at a particular location on a particular
chromosome and control the same characteristic,
such as blood type or color blindness.
Dominant alleles
are seen
as an uppercase of a letter.
Recessive alleles
are seen as a lower
case of a letter.
Homozygous-
You inherit the same version
of the gene from each parent, so you have
two matching genes.
Codominance
- When you have two copies
of the alleles that are both dominant.
Heterozygous-
You inherit a different
version of a gene from each parent. They do
not match.
Genotype-
A person's genotype is their
unique sequence of DNA. More specifically,
this term is used to refer to the two alleles a
person has inherited for a particular gene.
Phenotype
is the detectable
expression
Genotype
– a patient's clinical presentation
A
Punnett square
is a chart that allows
you to easily determine the expected
percentage of different genotypes in the
offspring of two parents.
Transcription
converts DNA into messenger RNA (mRNA).
Translation
then decodes mRNA into amino acids