Unit 6.2- Patterns of Inheritance Flashcards
Types of chromosome mutations:
- Deletion
- Inversion
- Translocation
- Duplication
- Non-disjunction
Translocation chromosomal mutation definition:
A piece of a chromosome breaks off and then becomes attached to another chromosome
Duplication chromosomal mutation definition:
Part of a chromosome may be duplicated
Non-disjunction chromosomal mutation definition:
One pair of chromosomes or chromatids fails to separate, leaving one gamete with an extra chromosome. When fertilised with a normal haploid gamete, the resulting zygote has one extra chromosome
Aneuplody defintion:
The chromosome number is not an exact multiple of the haploid number for that organism. Sometimes chromosomes or chromatids fail to separate during meiosis
Polyploidy definition:
If a diploid gamete is fertilised by a haploid gamete, resulting in a zygote that will be triploid
When does genetic variation occur in meiosis?
- Allele shuffling/ crossing over in prophase 1
- Independent assortment in anaphase 1 and 2
Heterozygous definition:
Not true-breeding; having different alleles at a particular gene locus on a pair of homologous chromosomes
Homozygrous definition:
True-breeding; having identical alleles at a particular gene locus on a pair of homologous chromosomes
Monogenic definition:
Determined by a single gene
Dyhybrid definition:
Involving two gene loci
Codominance definition:
Where both alleles present in the genotype of a heterozygous individual contribute to the individual’s phenotype
Sex-linked definition:
Gene present on one of the sex chromosomes
Autosomal linkage definition:
Gene loci present on the same autosome (non- sex chromosome) that are often inherited together
What genes form as a result of crossing over of autosomal genes?
Recombiant genes