Non-Mendelian Genetics: Non-Mendelian Genetics and Heredity Flashcards
Codominance
two dominant alleles are expressed at the same time
Incomplete Dominance
no allele is completely dominant. BLENDING of phenotypes occurs to make a 3rd phenotype.
–> Only assume heterozygous genotype represents blending if told so. Otherwise, always assume the heterozygous genotype shows for the same dominant phenotype as homozygous dominant.
Sex-linked Traits
traits found on a sex chromosome (X or Y), usually refers to X traits (because only males have Y)
Sex-linked Traits
Relationships between Parents and Children
- Fathers cannot pass sex-linked traits to their sons because males receive their X-chromosome from their mothers.
- Mothers can pass sex-linked alleles to both sons and daughters.
Sex-Linked Traits
Relationships between X and Y Chromosomes
- Most X-linked genes have no homologous loci on the Y chromosome.
- Most genes on the Y chromosome not only have no X counterparts, but they encode traits found only in males
- The X chromosome is larger than the Y chromosome, therefore there are more traits present on the X chromosome.
Pedigrees
tracks a specific trait within family history, squares represent males, circles represent females, unshaded (white) are unaffected, and shaded (black) are affected.
Autosomal Recessive Pedigrees
recognized because the trait skips a generation but is still equally shown in both genders.
Sex-linked Recessive Pedigrees
recognized by the trait skipping a generation and recognition that the trait is much more common in males. Specifically with this pattern, any affected female must have an affected father.
Pedigrees
Complicated Information about Pedigrees
- If the trait is identified as autosomal dominant, all unaffected individuals must be homozygous recessive
- All affected individuals must have at least one dominant allele
- People who marry into the families can either be identified as homozygous recessive or known with only one dominant trait (the other trait is unknown).
Carriers
FEMALES who has inherited a recessive allele of a gene that is linked to a genetic condition. However, she doesn’t show traits or symptoms of the condition because her second allele for that gene is normal.