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Biology~DNA, Inheritance & cell division
Genetic variation and inheritance~
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A gene is a section of
DNA
on a
chromosome
, codes for a particular
sequence
or
amino acid.
Most of our
characteristics
are controlled by
multiple
genes.
An allele is a
different
form of the same
gene.
Chromosomes
occur in pairs.
Most genes come in
pairs.
Each
allele
comes from the
parents
in
sexual reproduction.
If a person has two alleles that are the same they are called
homozygous.
(You can either be
Dominant
or
Recessive
)
If a person has two alleles that are different they are
heterozygous.
(have both a
dominant
and
recessive
allele)
The stronger allele is referred to as
dominant.
The weaker allele is referred to as
recessive.
A
genotype
is a set of alleles that an organism has, expressed as the
phenotype.
3 possible genotypes:
-BB
-Bb
-bb
A
phenotype
is the
visible
characteristic of an
organism.
2 possible phenotypes:
-Black
-Yellow
To determine the characteristic that an
offspring
may have we use a
punnet square.
The famous scientist that is known for his work on inheritance is
Mendel.
The dominant allele is written
first.
The first generation of a cross is referred to as the F1.
The definition of
self-pollinating
/
selfing
is when the
f1
genotype is
crossed
with itself.
The second generation is referred to as the
F2.
Chromosome pair number
23
determines the
sex
of an offspring.
If the
sex chromosomes
are the same the gender of a human would be a
female.
If the chromosomes are different the gender of a human would be a
male.
The female sex chromosomes are
XX.
The male sex chromosomes are
XY.
The possible number of sex chromosomes that a female can put into her egg is
1.
The possible number of sex chromosomes that a male can put into his sperm is
2.
The females is
X.
The
males
is X and Y.
The
father's sperm
determines the sex of the offspring.
Every time fertilisation happens, the probability of having a girl is
50
%.
Every time fertilisation happens, the probability of having a boy is
50
%.