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Gene
Section of DNA on a chromosome that controls a feature of one or more specific polypeptides or a functional RNA (rRNA and tRNA).
Locus
The specific linear position of a particular gene on a certain chromosome.
Allele
Alternative forms of a particular gene with different base sequences, and therefore different codes.
Homozygous
Situation or organism in which paired alleles are the same.
Heterozygous
Situation of organism in which paired alleles are different.
Dominant Allele
An allele that expressed itself in the phenotype in heterozygous organisms.
Recessive Allele
An allele that does not express itself in the phenotype in heterozygous organisms.
Co-dominance
Alleles which both contribute to the phenotype (i.e produce a blended effect) in the heterozygous condition.
Multiple alleles
if there are more than two alleles for each gene in the gene in the gene pool. NB. Only 2 chromosomes in a homologous pair so only 2 of the three or more alleles can be present in asingle organism.
Pure Breeding Strain
Group of organisms in which a certain characteristic is unaltered for generations, indicating that organisms are homozygous for that feature.
Monohybrid
Inheritance of a single pair of alleles.
Dihybrid
Inheritance of two pairs of alleles.
Haploid
Cell or nucleus containing single, unpaired chromosomes.
Diploid
Cell or nucleus containing pairs of homologous chromosomes.
Phenotype
The observable or biochemical characteristics of an organism, resulting from both its genotype and the effects of the environment.
Genotype
The combination of alleles present within the cells of an organism.
Heritable
Features determined by genes (rather than the environment) and therefore passed onto offspring.
Homologous
A pair of chromosomes, one maternal and one paternal, that have the same gene loci and therefore determine the same features. They are not necessarily identical as they may have different alleles. They are capable of pairing during meiosis.
Ratio
A measure of the relative size of two classes that is expressed as a proportion.
Sex-linked
Any gene that is carried on either the X or Y chromosome.
Autosomal linkage
The situation where two or more genes are carried on the same autosome.
Autosome
A chromosome which is not a sex chromosome.
Epistasis
This arises when the allele of one gene affects or masks the expression of another in the phenotype.
How many alleles per gene do diploid organisms carry
two
What is the phenotypic ratio of monohybrid inheritance between to heterozygotes
3:1
What is the phenotypic ratio of monohybrid inheritance between two heterozygotes
2:1:1
What is the Phenotypic ratio within a dihybrid cross between two parents who are heterozygous for both traits?
9:3:3:1
Why are males more likely to express a recessive sex-linked allele
Most sex-linked alleles are located on the X chromosome.
Therefore males only get one copy of the allele and will therefore express this characteristic even if it’s recessive
What is an example of polygenic inheritance
(One of the below answers), Eye colour, Height, hair colour
What are two examples of sex linked diseases
Colour blindness and haemophilia
What are the different blood types
IA, IB, IAB and IO
Which is the recessive blood type
IO
Which blood type is the universal donor
IO
Why is IO blood type the universal donor
As it has neither A nor B antigens on its cell surface membrane, it will not trigger an immune response from either blood groups
Which blood type is the universal acceptor
IAB
Why is IAB The universal acceptor
as it has both A and B antigens on its cell surface membrane it can accept blood donations from any blood group as they would not trigger an immune response
what are the two types of epistasis
Recessive and dominant