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Cards (26)
law of segregation
parent cell Pp yields
gametes
P and p,
homozygous
:
identical
alleles,
heterozygous
: two
different
alleles
law of independent assortment
during
gamete formation
, each pair of
alleles
separates
independently
dihybrid cross
cross
that looks at
2 traits
instead of just
1
rule of multiplication
determines the chance that
2 or more independent events will occur together in a specific combo
codominance
2 alleles affect the
visible appearance
of an organism in
separate
,
distinguishable
ways (
heterozygotes
express both alleles)
incomplete dominance
neither gene is completely dominant
;
heterozygotes
show a
distinct intermediate phenotype
(
traits
appear to be
combined
)
multiple alleles
gene
that codes for a
trait
can exist in more than
2 allelic forms
ex:
ABO blood types
(
3
options of a gene for
blood type
)
blood type A
AA
or
Ai
,
Anti-B
antibodies
blood type
B
BB
or
Bi
,
Anti-A
antibodies
blood type AB
AB
,
no antibodies
,
universal recipient
blood type
O
ii
,
Anti-A
and
Anti-B
,
universal donor
environmental impact
phenotype
depends on
genes
AND
environment
,
product
of a
genotype
is not a
rigidly defined phenotype
, but a range of
possibilities
ex:
hydrangeas
and
soil pH
multifactorial
many factors, both
genetic
and
environmental
, collectively influence
phenotype
polygenic inheritance
2
or more genes affect a single
phenotype
characteristic
quantitative characters
characters vary along a
continuum
(in a
gradient
)
chromosomal inheritance
genes located
near
each
other
on the same chromosome tend to be
inherited
together
; these are called
linked genes
offspring with a phenotype matching one of the parental phenotypes are called...
parental types
chromosomes are passed along as units meaning...
genes are inherited together
crossing over
occasionally breaks the
physical
connection
between specific alleles on the
same
chromosome
the farther that genes are...
the
higher
probability that a
crossing over event
will occur =
higher recombinant frequency
map units
one map unit equals to
1% recombination frequency
sex linked inheritance
genes
located on either
sex-chromosome
(mostly
X-linked
)
wild type
most commonly observed phenotype in nature
X-inactivation in female mammals
females inherit
2 X chromosomes
, but one of them is
randomly
inactivated
in
each cell
during
embryonic development
Barr body
inactive
X in each cell
condenses
into a
compact
object, occur
randomly
in an
embryo
, so females have a
mosaic
of
two
types of cells
ex:
tortoise shell cats
on a pedigree, if more males/females are affected, then...
the trait is
sex linked
(usually male because they only have
one X
)