Dominant trait is the trait that shows through,masks others.
Recessive trait is the trait that is being masked by the dominant.
Traits are expressed characteristics.
Alleles are different forms of each gene.
Gregor Mendel, named the father of genetics in 1851, that breaded pea plants and discovered Mendel discovered the basic principles of heredity and laid the mathematical foundation for genetics.
Gregor found out that there was 7 characteristics in pea plants.
Phenotype is the physical thing being seen.
Genotype is the genetic thing you consist of.
Example of a Homozygous parent is RR or rr
Example of a Heterozygous parent is Rr
F1 generation consists of all dominant phenotypes.
F1 generation + F1 generation= F2 generation
Gregor Mendel had 3 major laws that consisted of-
Law of dominance
For each trait, one version is dominant to the other (recessive)
Law of segregation
When an individual makes gametes (sex cells), The alleles separate from each other
Law of independant assortment
one had nothing to do with the other
Monohybrid cross is the crossing of 1 trait.
Steps for punt square-
Write/identify parent alleles
do punnit square
write phenotype/genotype
Karyotype is a full image of your chromosomes before meiosis and during cell division.
Sex chromosomes have 23 pairs.
Male= XY
Female= XX
Test cross is a way to define whether a organism that expresses a dominant trait is homo or hetero.
Co-dominance is where there are ATLEAST two dominant alleles and one recessive.
Incomplete dominance is when one is missing.
Blood types-
A
B
AB
O
Only way to be one type of blood is for both parents to give the same blood.
Genotype for Blood type- A : Homo(Ia,Ia) + Hetero(Ia, i)
Genotype for blood type- B: Homo(Ib,Ib) + Hetero(Ib, i)
Genotype for blood type- AB: (Ia,Ib)
Genotype for blood type- O: (ii)
Which blood type is the universal donor? - O
What type of blood can type AB get?- All blood
Male
XY= normal
Xc Y= affected
Female
XX= normal
X Xc= carrier
Xc Xc= Both affected
Examples of sex linked trait deformity-
hemophilia
red-green color blindness
congenital night blindness
some high blood pressure genes
Duchenne muscular dystrophy
Fragile X syndrome.
Dihybrid cross is cross of two traits
Nondisjunction is when chromosomes fail to separate properly.
What affects does nondisjunction have on people?
extra chromosomes
disorders
meiosis cycle interference
Chromosomal mutations happen in the gametes
Point mutations happen in the somatic cells
Chromosomal mutations affect the OFFSPRING
Point mutations affect YOU
Chromosomal mutations result in an addition or deletion of genes
These mutations can lead to various genetic disorders or developmental issues depending on the genes involved.
Nondisjunction is the only thing that can change the number of chromosomes added or lost
Trisome is when there are 3 chromosomes in one cell when there should be 2
Monosome is when there are 1 chromosome in a cell when there should be 2
Nondisjunction happens in meiosis 1 and 2
Nondisjunction disorders due to chromosomes include:
turners syndrome- monosomy
down syndrome- trisomy of 21st pair
Kleinfelds syndrome- trisomy of 23rd pair
triple x syndrome- trisomy of 23rd pair
Jacobs syndrome- trisomy of 23rd pair
Edwards syndrome- extra 18th pair
Patav syndrome- extra 13th pair
Karyotype is a picture of your chromosomes that can only be taken during cell division.
Male shape
Full square- affected
Empty square- unaffected
Female shape
Full circle- affected
Empty circle- unaffected
Symbols and rules
Married= Full square connected to full circle
Incest marriage= full square half connected to a full circle
Siblings= two full squares connected by two lines
Dead= line through full square or full circle