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describe
describe

... combination of sex chromosomes in the zygote dictates the sex of the child: a zygote that inherits an X chromosome from both the mother and father will be female (XX). A zygote that receives an X chromosome from the mother and a Y chromosome from the father will be male (XY). In humans,Y carries the ...
Mutations and Disorders worksheet-ANS
Mutations and Disorders worksheet-ANS

... Use the following symbols to identify the genetic disease below; symbols may be used once, more than once or not at all. ...
1. Introduction 2. Fact or Fiction?
1. Introduction 2. Fact or Fiction?

... cell of the human body contains and that, together, contain all the genes. Other species have more or fewer chromosomes. ...
Slides on chromosomal changes
Slides on chromosomal changes

... Monosomy 2n-1 (lethal in humans with exception of X0) X0 – Turner syndrome – phenotypic effects including some level of congitive impairment Trisomy 2n+1 XXY – Klinefelter syndrome, Males, lower IQ, sterile XYY – once thought to have enhanced violence. Not clear XXX – females normal Trisomy 21 – Dow ...
Nature vs. Nurture - Elizabeth School District
Nature vs. Nurture - Elizabeth School District

... Answer True or False for the following questions  1. Even complex human traits are determined by a single gene  2. People’s divorce risks are about 50% attributable to genetic factors  3. Adoptees’ traits bear more similar to their adoptive parents than to their biological parents  4. Two differ ...
NAME CHAPTER 14 QUESTIONS Human Genome MULTIPLE
NAME CHAPTER 14 QUESTIONS Human Genome MULTIPLE

... A person that has ONE copy of an AUTOSOMAL RECESSIVE allele and does not express the trait, but can pass it along to his/her offspring is called a __________________. A. mutant B. carrier C. gene marker The failure of homologous chromosomes to separate during meiosis is called ____________________ A ...
Patterns of Inheritance
Patterns of Inheritance

... M. Explain what is meant by a vector. How were vectors expected to cure cystic fibrosis? What problems occurred, and what is the current outlook in using gene therapy? 13.3 Genes On Chromosomes N. The chromosomal theory of inheritance states that it is on chromosomes that Mendel’s “factors” reside. ...
3.3.1: How is DNA Passed Through the Generations?
3.3.1: How is DNA Passed Through the Generations?

... o Both cells split into two, with the resulting cells each containing a single chromosome set. (Half the chromosomes of the parent cell. This is how each egg cell and sperm cell contains half the chromosomes of body cells. Therefore, when the sperm and egg combine, they contain the correct number of ...
Chromosomal Inheritance
Chromosomal Inheritance

... • Because hermaphrodites have two Xs, they also have a double dose of every gene on the X, even the ones that have nothing to do with sex. • Genes make proteins, so hermaphrodites stand to produce twice as much X-encoded protein as males. • Such genetic imbalance can be harmful in any organism: Down ...
Chromosomal Aberrations
Chromosomal Aberrations

... • About 40% of conceptions with Klinefelter syndrome survive the fetal period. • In general, severity of somatic malformations in Klinefelter syndrome is proportional to the number of additional X chromosomes; mental retardation and hypogonadism are more severe in 49,XXXXY than in 48,XXXY. • Mortali ...
Genetic Disease
Genetic Disease

... 12) Twin studies show that pairs of identical (monozygotic) twins, with their identical genes, have a higher-than-average chance of sharing the same orientation compared to pairs of randomly selected individuals; the average (or "background") rate of the trait in any given population is just under 8 ...
Slide 1 - Brookwood High School
Slide 1 - Brookwood High School

... the sex chromosomes  Y chromosome much smaller than X so many genes only found on X  Males express all X-linked alleles since they have only one X chromosome – even recessives  Ex. Color blindness, hemophilia ...
Notes - MyWeb
Notes - MyWeb

... Gene locus with alleles B or b determines coat color Which allele at each locus is dominant? ...
Multiple Alleles and Polygenic Inheritance
Multiple Alleles and Polygenic Inheritance

... The human Y chromosome is much smaller and appears to contain only few genes. Father determines the sex of the offspring The chance is always 50-50 for either sex A recessive gene has no matching gene on the Y More Sex linked disorders are found in males ...
Chapter 14 Reading Guide
Chapter 14 Reading Guide

... What scientist was particularly important to understanding biological inheritance? What kind of plants did the scientist above use to conduct his studies? What is fertilization? What does “true-breeding” mean? What are hybrids? What was Mendel’s first conclusion from his experiment? What are the che ...
LAB 10-A - BrainMass
LAB 10-A - BrainMass

... The resulting cell contains one chromosome of each pair There is pairing of homologous chromosomes Each chromosome duplicates itself Each daughter cell contains the same kind and number of chromosomes as the parent cell. e. Haploid cells are formed from diploid cells f. The nuclear membrane disinteg ...
Cellular Reproduction
Cellular Reproduction

... Of the 23 pairs of chromosomes in human somatic cells, 22 pairs are the same. These chromosomes are called autosomes-not directly involved in determining the sex. The Sex Chromosomes, X,Y, determine the sex of the organism. These chromosomes are called sex chromosomes. A combination of XX is a fema ...
Section 6-1 Chromosomes
Section 6-1 Chromosomes

... as X (female) and Y (male). • Genes that cause a fertilized egg to develop into a male are on the Y chromosome. • XX – female; XY – male • The mother always gives an X chromosome. The father will give either an X or Y chromosome, so he determines the offspring’s gender. • Some species have no Y chro ...
BIOL
BIOL

... 1. They are identical. 2. In each cell there are two pairs of homologous chromosomes--one pair from each parent. 3. The homologous pairs of chromosomes pair up and undergo recombination during prophase of mitosis. 4. They contain all of the same genes but not necessarily the same alleles. ...
BUILT-IN BIOSAFETY DESIGN Ollie Wright - 29/04/13
BUILT-IN BIOSAFETY DESIGN Ollie Wright - 29/04/13

... per cell generation ...
X Chromosome
X Chromosome

... • The expression of genes on the sex chromosomes differs from the expression of autosomal genes. • Genes located on the sex chromosomes are called sex- linked genes or X-linked genes. • Males express all of the alleles on both sex chromosomes. • In females one of the two X chromosomes is randomly tu ...
Name - O. Henry Science
Name - O. Henry Science

... Each chromosome is divided into small sections called genes. Genes are the basic units of heredity. They carry codes that control the individual traits that the offspring inherit. Traits in humans such as eye color, height, skin color, face shape, shape of ear lobes, hairlines, and tongue rolling ar ...
Bacteria
Bacteria

... * No nucleus, chromosome is found in dense area, nucleoid * May also have xtra DNA in smaller circles, plasmids. * Division- DNA copies itself in both directions until entire circle has been replicated. - Then divides by binary fission. * Divide very quickly under good conditions. * E. coli divides ...
Drosophila - mccombsscience
Drosophila - mccombsscience

... Reddish-orange eyes and miniature wings almost always inherited together Observed this trend in many genes Grouped all the fly’s genes into four linkage groups Drosophila has four linkage groups and four pairs of chromosomes ...
Genetics Notes HONORS
Genetics Notes HONORS

... adult tissues and does NOT get passed down to future offspring • Usually not expressed in the adult • Cancer is the exception, it is expressed in the adult tissues, but still does not get passed down to offspring ...
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Y chromosome



The Y chromosome is one of two sex chromosomes (allosomes) in mammals, including humans, and many other animals. The other is the X chromosome. Y is the sex-determining chromosome in many species, since it is the presence or absence of Y that determines the male or female sex of offspring produced in sexual reproduction. In mammals, the Y chromosome contains the gene SRY, which triggers testis development. The DNA in the human Y chromosome is composed of about 59 million base pairs. The Y chromosome is passed only from father to son. With a 30% difference between humans and chimpanzees, the Y chromosome is one of the fastest evolving parts of the human genome. To date, over 200 Y-linked genes have been identified. All Y-linked genes are expressed and (apart from duplicated genes) hemizygous (present on only one chromosome) except in the cases of aneuploidy such as XYY syndrome or XXYY syndrome. (See Y linkage.)
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