Transcript Pedigree
Patterns of Heredity and Human
Genetics
Pedigree – made up
of a set of symbols
that identify males
and females, the
individuals affected
by a trait being
studied and family
relationships
(Family Tree)
Pedigree
Cystic Fibrosis (CF)
Lethal genetic
disorder among
whites
Thick mucus in
lungs and
digestive tract
Defective protein
in the plasma
membrane
Tay Sachs Disease
Missing enzymes
that breaks down
lipids
Causes blindness,
progressive loss
of movement and
mental
deterioration
Phenylketonuria (PKU)
Missing enzyme
needed to break
down amino acid
phenylalanine to a
different amino acid
tyrosine
Damages central
nervous system
Cannot break down
milk, results in
retardation
Tongue Rolling
Hapsburg Lip - The lower lip and chin
protrude, sometimes forcing the mouth
open.
Earlobe (Free-hanging)
Hitchhiker’s Thumb
Thick Lips
Huntingtons Disease
Double Jointedness
Lethal, appears between ages 30 – 50
Breakdown of portions of the brain
Incomplete
Dominance
Inheritance
pattern where the
phenotype of a
heterozygote is
intermediate
between those of
the 2
homozygotes
Ex.
RR (Red
Flowers) x
R’R’ (white
flowers) = F1
offspring are
pink
R
R
R'
RR'
RR'
R'
RR'
RR'
With codominance, a cross
between organisms with two
different phenotypes produces
offspring with a third phenotype
in which both of the parental
traits appear together. .
All organisms have:
Autosomes – non-sex
chromosomes that carry all
characteristics except sex
Sex Chromosomes – two
chromosomes that determine sex
XX – Female, X is rod shaped
XY – Male, Y is J or hook shaped
Humans – 46 chromosomes
Autosomes – 44 chromosomes
Sex Chromosomes – 2 chromosomes
Drosophila – 8 chromosomes
Autosomes – 6 chromosomes
Sex Chromosomes – 2 chromosomes
Traits controlled by genes located on
sex chromosomes
Those carried on the X and Y chromosome
1. Hemophilia – free bleeders (X chromosome)
Person lacks the gene needed for clotting of
the blood
2. Colorblindness – not being able to determine
the difference between colors, usually red and
green, usually found in males, caused by
recessive gene on X chromosome
Both conditions are recessive and appear most
often in males. A pedigree chart is used to trace
genetic traits in families