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Genetics
The study of how
genes
bring about
characteristics
, or traits, in living things and how those characteristics are inherited
Genes
Specific sequences of
nucleotides
that code for particular
proteins
Meiosis
The process where the
diploid
number of chromosomes is
reduced
to a haploid number
Sexual reproduction
The process where haploid gametes come together to
reestablish
the
diploid
condition
Gregor Mendel
Augustinian monk who developed the science of
genetics
Mendel
performed his experiments in the 1860s and 1870s, but the scientific community did not accept his work until early in the
twentieth
century
Mendelian
genetics
The science of genetics based on the
principles
established by Mendel
Molecular genetics
Another branch of biology distinct from classical
Mendelian
genetics
Diploid
cells
Cells that have a
double
set of
chromosomes
, one from each parent
Haploid cells
Cells that have a single set of
chromosomes
, formed through
meiosis
Gametes
Haploid
sex cells formed through
meiosis
Alleles
The different
forms
of a
gene
Genome
The set of all genes that specify an organism's
traits
Genotype
The
gene
composition of a living
organism
Phenotype
The expression of the genes
Homozygous
When two
identical
alleles are present for a particular
characteristic
Heterozygous
When two
different
alleles are present for a particular
characteristic
Dominant
allele
The allele that expresses itself when present with a
recessive
allele
Recessive
allele
The allele that is "overshadowed" and only expresses itself when two
recessive
alleles exist together
Pure
lines
Populations of
homozygous
individuals for particular
characteristics
Parent generation
Pure-line
pea plants that are
cross-pollinated
F1 generation
The offspring of the
parent
generation
cross
F2
generation
The offspring of the
F1
generation cross
Mendel's laws of genetics
Law of
dominance
2. Law of
segregation
3. Law of
independent assortment
Genetic cross
Also called a
Mendelian cross
, a way to predict the probability of
inherited traits
in offspring
Punnett
square
A
boxed
figure used to determine the probability of genotypes and
phenotypes
in the offspring of a genetic cross
Incomplete dominance
When two characteristics are equally
expressed
, rather than one dominating the other
Multiple alleles
When more than
two
alleles exist for a particular
characteristic
in a population
Polygenic inheritance
When a characteristic is determined by an
interaction
of
genes
on several chromosomes or at several places on one chromosome
Gene
linkage
When genes that are located close together on a
chromosome
are
inherited
together
Sex linkage
When a gene occurs on a
sex
chromosome, usually the
X
chromosome
DNA
Deoxyribonucleic
acid, consisting of two long nucleotide chains in a
double helix
structure
Colorblindness
Expresses itself in the
male
Hemophilia
Blood disease where
blood
does not clot normally because an important
blood-clotting protein
is missing
The gene for
hemophilia
occurs on the
X chromosome
Females
May be a carrier of
hemophilia
but normally do
not
express it
Males
Have no offsetting gene on the
Y
chromosome, so the gene for
hemophilia
expresses itself
Most cases of hemophilia occur in
males
DNA
Consists of two long
nucleotide
chains that twist around one another to form a
double helix
Nucleotide
Consists of a
nitrogenous
base, a
phosphate
group, and a molecule of deoxyribose
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