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Genetic Code
consists of DNA, chromosomes, and genes
Phenotype
directly observable characteristics of an individual, affected by both genetics and environment
Genotype
the complex blend of genetic information that determines our species and influences all our unique characteristics
Chromosomes
rodlike structures within the cell nucleus that store and transmit genetic information; humans have 23 pairs (46 total)
DNA
long, double-stranded molecules that make up chromosomes and carry genetic instructions
Gene
a segment of DNA along the length of the chromosome that contains instructions for making proteins
Gametes
s*x cells (sperm in males, ova in females) containing 23 individual chromosomes
Meiosis
the cell division process through which gametes are formed, halving the number of chromosomes so that offspring receive 23 from each parent
Zygote
the single cell formed when a sperm and ovum unite at conception
0-2 weeks
Autosomes
the matching pairs of chromosomes that are not s*x chromosomes
S*X chromosomes
the 23rd pair of chromosomes that determines the genetic sx of the individual
xx in females, xy in males
Fraternal twins (Dizygotic)
twins resulting from the release and fertilization of two separate ova; genetically no more alike than ordinary siblings
Identical twins (Monozygotic)
twins created when a single zygote duplicates and separates into two clusters of cells, resulting in identical genetic makeup
Allele
each of two or more alternative forms of a gene located at the same place on parallel chromosomes
Homozygous
having two identical alleles at the same locus on a pair of chromosomes
Heterozygous
having two different alleles at the same locus on a pair of chromosomes
Dominant-Recessive inheritance
a pattern in which only one allele (dominant) affects the child’s traits, while the second allele (recessive) has no effect
Carrier
a heterozygous individual who can pass a recessive trait to offspring without expressing the trait themseleves
Incomplete dominance
a pattern of inheritance in which both alleles are expressed in the phenotype, resulting in a combined trait or intermediate phenotype (ex. sickle cell trait)
X-linked intheritance
a pattern of inheritance where a harmful allele is carried on the X chromosome; males are more likely to be affected because they have only one X chromosome
Genomic imprinting
a pattern of inheritance in which alleles are chemically marked so that one pair member, either father or mother, is activated, regardless of its makeup
Mutation
a sudden, permanent change in a segment of DNA
Polygenic inheritance
a pattern of inheritance in which many genes affect the characteristic in question (ex. intelligence, personality)
Socioeconomic status (SES)
a measure of a person’s or family’s social position and economic well-being, combining years of education, prestige/skill of job, and income
Collectivist societies
cultures in which people define themselves as part of a group and prioritize group goals over individual goals
Individualistic societies
cultures in which people think of themselves as separate entities and are largely concerned with personal needs and goals
Epigenesis
development resulting from ongoing, bidirectional exchanges between heredity and all levels of the environment
Epigenetics
the study of environmental influences that modify gene expression without altering the underlying DNA sequence
Niche picking
a type of active gene environment correlation in which individuals actively choose environments that complement their hereditary
Down syndrome (Trisomy 21)
caused by an extra 21st chromosome; results in intellectual disability, distinct physical features, and health risks
Gene-Environment interaction
the concept that individuals, because of their unique genetic makeups, respond differently to identical environmental conditions
Gene-Environment correlation
the idea that our genes influence the environments to which we are exposed (includes passive, evocative, and active/niche picking correlations)
Heritability estimates
measures obtained from kinship studies that estimate the proportion of individual differences in complex traits due to genetic factors
Kinship studies
studies comparing the characteristics of family members to determine genetic influences