Ch. 11-14 Genes and Chromosomes Test Review Flashcards
homologous chromosomes that are same or similar chromosomes in males and females
autosomes
how many Autosomes does a human have?
44
chromosomes that are different in males and females
sex chromosomes
how many sex chromosomes does a human have?
2
traits that are produced through the interaction of several genes
polygenic traits
only gets 1 sex chromosome (X). Appears female but sex organs do not develop at puberty
Turner Syndrome
what is a Karyotype for Turner Syndrome?
45 X or 45 X0
gets two X’s and 1 Y. Appear male but are sterile
Klinefelter Syndrome
what is a karyotype for klinefelter syndrome?
47 XXY
a gene with more than two alleles
multiple alleles
a gene located on one of the sex chromosomes
sex linked genes
both alleles are active so both are expressed
codominance
the active allele does not completely dominate over the inactive allele so the outcome is in between
incomplete dominance
a trait that is caused by a gene whose expression is different in males and females
sex influenced traits
in male patterned baldness, what does BB stand for?
normal
in male patterned baldness, what does Bb stand for?
men are bald; women are normal
in male patterned baldness, what does bb stand for?
both are bald (rare)
mistakes in gene information transfer
mutations
involve segments, whole or sets of chromosomes
chromosome mutations
part of the nonhomologous chromosome breaks off and attaches to another
translocation
mistakes that affect the reproductive cells
germ mutations
mistakes that affect body cells
somatic mutations
a segment is replaced
a. original chromosome- ab: cdefg
b. mutated chromosome- ab:cdefefg
duplication
changes that affect one single protein
point mutation
oriented in the reverse of its usual direction
original chromosome: abc:defg
mutated chromosome: aed:cbfg
inversion
the loss of a part of a chromosome
original chromosome: abc:defg
mutated chromosome: abc:deg
deletion
failure of chromosomes (Meiosis I) or chromatids (Meiosis II) to separate properly and the results are gametes with too few or too many chromosomes
nondisjunction
what is the karyotype for a person with nondisjunction?
47 XX or 47 XY
a protein is inserted or deleted so it changes the sequence completely
frameshift mutation
what is essential in sex determination?
the X chromosome
Give all the possible genotypic combinations for a person with A blood?
AA or AO
Give all the possible genotypic combinations for a person with B blood?
BB or BO
Give all the possible genotypic combinations for a person with O blood?
OO
Give all the possible genotypic combinations for a person with AB blood?
AB
a universal donor has to have what blood type?
O, because it has no antigens
SEE REVIEW GOOGLE FORM TO STUDY FOR MORE
HJK:LOPQ
deletion
HJJK:LMNOPQ
duplication
HML:KJNOPQ
inversion (MUST WORK OUT USING MODEL ON TEST)
HJK:LMNOPQ HJK:LDEOPQ
AB:CDEFG AB:CMNFG
translocation
take out the E in the first THE to make a frameshift
THE RAT SAT AND ATE THE FAT
THR ATS ATA NDA TET HEF AT