RULES OF INHERITANCE - NON - MENDELIAN Flashcards

1
Q

Any pattern of inheritance in which traits do not segregate according to Mendel’s laws

A

non-mendelian genetics

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2
Q

Describes the inheritance of traits linked to single genes on chromosome in nucleus

A

non-mendelian genetics

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3
Q

these are conditions affected by several loci

A

non-mendelian genetics

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4
Q

A condition when during the heterozygous condition the dominant allele does not completely overpower the recessive allele but has blending of trait

A

incomplete dominance

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5
Q

A condition when during the heterozygous condition the dominant allele does not completely overpower the recessive allele and has no blending of trait

A

codominance

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6
Q

Dominant allele only partially mask the presence of recessive trait

A

incomplete dominance

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7
Q

Neither allele is dominant or recessive

A

codominance

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8
Q

these genes does not produce any antigen on the RBC

A

amorph/silent gene

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9
Q

what are the genotypes of blood type A?

A

AA or AO

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10
Q

what are the genotypes of blood type B?

A

BB or BO

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11
Q

what are the genotypes of blood type AB?

A

A B

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12
Q

what are the genotypes of blood type O?

A

OO

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13
Q

Inheritance pattern for traits that are controlled by more than one gene

A

polygenic inheritance

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14
Q

there is a phenotype gradient in this kind of inheritance

A

polygenic inheritance

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15
Q

Multiple genes affects the inheritance of one trait

A

polygenic inheritance

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16
Q

Genes capable of causing death of organism carrying them

A

lethal genes

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17
Q

The effect on phenotype is profoundly negative and causes the organism to exhibit many disadvantageous characteristics which can lead to death

A

lethal genes

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18
Q

Death from genetic disease can occur at any stage of development or life.

A

lethal genes

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19
Q

this disease is caused by an imitation in the enzyme hexosaminidase-Ab having a buildup of fatty acid in the cell and limit the life span to 3-5 years

A

tay-sachs disease

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20
Q

this disease is characterized with progressive breakdown of nerve cell in the brain and limits the life span from 10-25 years only

A

huntington’s disease

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21
Q

if two people with achondroplasia have children, each child has how many chances of inheriting achondroplasia?

A

2/3

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22
Q

if two people with achondroplasia have children, each child has how many chances of having a normal height?

A

1/3

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23
Q

if two people with achondroplasia have children, each child has how many chance of dying as embryos?

A

1/4

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24
Q

if one person with achondroplasia had a children with a normal person how many chances does each child inherits achondroplasia?

A

1/2

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25
if one person with achondroplasia had a children with a normal person how many chances does each child have a normal height?
1/2
26
These charts are used to display family relationships and depict which relatives have specific phenotypes and sometimes genotypes
pedigrees
27
Represents relationship and sometimes traits
pedigrees
28
Interaction between alleles in heterozygotes
patterns of inheritance
29
- one allele controls the phenotype - one parent must have the trait - does not skip generation
dominant
30
- does not control the phenotype - not expressed in heterozygous - neither parent is required to have the trait since they can be heterozygous
recessive
31
what is the exception in recessive allele for it to be expressed even in heterozygotes?
sex-link inheritance (x-link or y-link)
32
the gene in question is located on one of the numbered chromosome or non-sex chromosome
autosomal
33
what is the ratio of autosomal inheritance between men and women
50/50
34
Transmission of traits depends on the genes in sex chromosome
x-linked/sex-linked
35
what transmission is not observed in sex-link inheritance?
male-to-male transmission
36
One mutated copy of the gene in each cell is sufficient for a person to be affected
autosomal dominant
37
male & female can transmit the trait to their offspring and does not skip generation
autosomal dominant
38
both parents are affected and homozygote for dominant condition is severe
autosomal dominant
39
Need 2 mutated copies of gene for it to manifest
autosomal recessive
40
affected person can have unaffected parents (carrier)
autosomal recessive
41
in autosomal recessive, if you have heterozygous parents, what is the ratio of the progeny that will be affected?
1/4
42
this show fewer affected individual and skips generation
autosomal recessive
43
what type of inheritance is involved in huntington disease?
autosomal dominant
44
what type of inheritance is involved in neurofibromatosis?
autosomal dominant
45
what type of inheritance is involved in cystic fibrosis?
autosomal recessive
46
what type of inheritance is involved in albinism?
autosomal recessive
47
there is no male to male transmission and it is more common in female
x-linked dominant
48
in x-linked dominant, if the father is affected, which offspring will inherit the gene?
daughters only
49
in x-linked dominant, if the mother is affected, which offspring will inherit the gene?
son and daughter
50
this has severe effect in male because there is no other allele to mask its effects
x-linked dominant
51
this always manifests in males but is rarely expressed in heterozygous female; skipping of generation
x-linked recessive
52
affected sons are born to affected mother
x-linked recessive
53
there is no male-male transmission but all daughters of affected father will become carrier
x-linked recessive
54
what type of inheritance is involved in hemophilia A?
x-linked recessive
55
what type of inheritance is involved in G6PD?
x-linked recessive
56
this is also called as holandric inheritance and only males are affected
y-linked recessive
57
it is passed from father to all sons and does not skip generations
y-linked recessive
58
Mutations in mitochondrial DNA
mitochondrial inheritance
59
Inherited through the maternal line
mitochondrial inheritance
60
Only daughters can pass it to their children but can affect both male and female offspring
mitochondrial inheritance