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CHAPTER 12 GENETICS
CHAPTER 12 GENETICS

... • The chromosomes carry the genetic information. • Eukaryotic chromosomes contain DNA and protein • The chromosomes are so named because they may be stained by certain dyes • When cells are not dividing, the genetic material is decondensed and is called chromatin • When cells are dividing, the genet ...
Genetics
Genetics

... an_Genome/posters/chromosome/chooser. shtml ...
Class - Educast
Class - Educast

... shades of red and green (usually blue-green). Their visual acuity (ability to see) is normal. There are no serious complications; however, affected individuals may not be considered for certain occupations involving transportation or the Armed Forces where color recognition is required. Males are af ...
Genetics Slides
Genetics Slides

... usual 24 or fewer, resulting in an abnormal form of protein known as huntingtin • If there are >60 CAGs, symptoms appear earlier • If just 36-38, symps may not occur until old age • CAG repeats in genes also occur in several other neurodegenerative conditions. ...
Genetics Table Simplified
Genetics Table Simplified

... Skin color is determined by three sets of genes on chromosomes #'s 1, 2, and 4. The dominant genetic code, gene "A" translates into a protein called melanin. This dark pigment is like a natural UV blocker. The greater the number of dominant genes one has, the greater the amount of melanin, the darke ...
1 - Webcourse
1 - Webcourse

... b) What are the genotypes of each of the 3 phenotypic classes amongst their children? c) Could the elliptocytosis and Rh loci be on the same chromosome? If so, estimate the map distance between them. d) Suppose, for the sake of argument that the parents of the mother (maternal grandparents of the 1 ...
Mitosis Prelab
Mitosis Prelab

... Watch the animations (there are 10 of them) read the info and answer the following questions; (not in order) Cell division consists of what two processes?. Mitosis is divided into what four phases? What is cytokinesis? What do motor proteins do to the daughter chromosomes during anaphase? What is a ...
The F plasmid and conjugation
The F plasmid and conjugation

Genetics Unit 2 – Transmission Genetics
Genetics Unit 2 – Transmission Genetics

... A) Sickle Cell Anemia B) Familial Hypercholesterolemia 3. _______________________ – both alleles are expressed A) AB blood type 4. Epistasis – one _______________ or affects the expression of a different gene. A) Bombay phenotype – some people have Type ___ blood, but not genotype ___ due to __ and ...
Gene-and-Chromosome-Mutations
Gene-and-Chromosome-Mutations

... and therefore the rest of the amino acid sequence ...
Multiple alleles
Multiple alleles

... Summing It Up: Mendel’s Principles 1. Parents pass on characteristics, sexually, through genes to their offspring 2. When there are multiple alleles (appearances) for one gene, some are dominant & some are recessive 3. During formation of parental gametes, alleles are segregated into separate gamet ...
1a.Genetics Key Terms
1a.Genetics Key Terms

... The allele that masks the effect of the recessive allele. An individual only needs one copy of this allele for it to be expressed (see in the phenotype) ...
Word file
Word file

... interactions between expanded genes (intervening steps are not shown). Green arrows represent the proposed pathway by which metabolism of hormones may influence physiology. It is not assumed that all of these genes will influence physiology or behaviour at any one time point. The diagram represents ...
lecture notes
lecture notes

...  Eukaryotes : ‘diploid’ having pairs of attached chromosomes. Each is the same except having possibly different versions of genes (alleles)  One allele may dominate over other (for example, black hair over blonde) or may work together (for example, blood group A & B giving rise to AB) Eukaryotes  ...
Homologous chromosomes
Homologous chromosomes

... two alleles that are the same at a specific locus. Ex: (RR or rr) – Heterozygous describes two alleles that are different at a specific locus.Ex: (Rr) – A dominant allele is expressed as a phenotype (visible trait) when at least one allele is dominant. – A recessive allele is expressed as a phenotyp ...
Document
Document

...  Usually must use a wheelchair by age 12  Death, age ~20 from respiratory infection or cardiac failure ...
Date Monday 5/5 Tuesday 5/6 Wednesday 5/7 Thursday 5/8 Friday
Date Monday 5/5 Tuesday 5/6 Wednesday 5/7 Thursday 5/8 Friday

... About 1 in 150 babies is born with a chromosomal abnormality. These abnormalities are caused by errors in the number or structure of chromosomes. There are many different chromosomal abnormalities. Many children with a chromosomal abnormality have mental and/or physical birth defects. Understanding ...
Relating Mendel`s Laws to Meiosis Name
Relating Mendel`s Laws to Meiosis Name

... 4. Each time we add a gene it doubles what we had. So 2 genes were 2 x 2 = 22 = 4, 3 genes is 4 x 2 = 23 = 8 and so on until we get to 22 genes. That’s 222= 4, 194,304 unique combinations. That’s just possible sperm or eggs. Combine those and you get a possible 17 trillion unique children from one c ...
Achondroplasia Β-Thalassemia Cystic Fibrosis
Achondroplasia Β-Thalassemia Cystic Fibrosis

... absorption by regulating the interaction of the transferrin receptor with transferrin. The most common HFE gene mutation in patients with HH is C282Y, followed by H63D. Up to 90% of HH patients are either homozygotes (C282Y/C282Y) or compound heterozygotes (C282Y/H63D), with the proportion varying d ...
The Story of pRB
The Story of pRB

... c. In hereditary RB, one mutation is inherited through the germ cells, and one mutation occurs in somatic cells (e.g. the retina) In sporadic RB, both mutations occur in somatic cells This fit the idea of a recessive tumor suppressor gene i.e. +/- cells are normal, and -/- cells become cancerous d. ...
DNA methylation
DNA methylation

... • Imprinted vs. random (TE vs. ICM) • Xist non-coding RNA (~15kb - mouse)– in cis („way-stations“?) • Xist regulated by antisense transcript Tsix • Inactive X form „Barr Body“ – H3K27-3Me, macroH2A, Ub-H2A, promoter hypermethylation, general transcriptional silencing … 46 XX ...
$doc.title

... During  meiosis,  two  chromosomes,  one  from  mom  and  one  from  dad,   twist  around  each  other     Large  segments  of  DNA  are  exchanged  and  recombined   Gamete  is  formed,  each  carries  copies  from  both  sides  of ...
Cell Growth and Genetics review on PDF File
Cell Growth and Genetics review on PDF File

... when chromosomes would most likely fail to separate. • Most likely chromosomes would fair to separate during anaphase I or Anaphase II. In anaphase, chromosomes (anaphase I) or sister chromatids (anaphase II) are supposed to separate, or move AWAY from each other. This is called Nondisjunction. • Pa ...
Study Guide: Lecture 1 1. What does “GMO” stand for and what does
Study Guide: Lecture 1 1. What does “GMO” stand for and what does

... 1. What does “GMO” stand for and what does it mean? 2. What is the meaning of a formula such as 2n = 2x = 18? a. How many chromosomes are there in a pollen grain of a plant with this formula? b. How many chromosomes are there in a leaf cell of a plant with this formula? c. What ploidy level is a pla ...
gene linkage probs
gene linkage probs

... Chapter 12.2 - Gene Linkage Different alleles exist because any gene is subject to mutation Wild type is a term used for the most common allele in the population. (+) Other alleles, often called mutant alleles, may produce a different phenotype An alternate form of designating alleles. Alleles that ...
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X-inactivation



X-inactivation (also called lyonization) is a process by which one of the two copies of the X chromosome present in female mammals is inactivated. The inactive X chromosome is silenced by its being packaged in such a way that it has a transcriptionally inactive structure called heterochromatin. As nearly all female mammals have two X chromosomes, X-inactivation prevents them from having twice as many X chromosome gene products as males, who only possess a single copy of the X chromosome (see dosage compensation). The choice of which X chromosome will be inactivated is random in placental mammals such as humans, but once an X chromosome is inactivated it will remain inactive throughout the lifetime of the cell and its descendants in the organism. Unlike the random X-inactivation in placental mammals, inactivation in marsupials applies exclusively to the paternally derived X chromosome.
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