Genetic diagnosis 1 (Lucy) Flashcards

1
Q

What ar ethe 4 types of genetic diseases that can arise from point mutations?

A
  • Cystic fibrosis
  • Phenylketonuria
  • Achrondoplasia
  • Osteogenesis imperfecta
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2
Q

What type of disease is cystic fibrosis?

A

Loss of function, recessive

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3
Q

What type of disease is phenylketonuria?

A

Loss of function, recessive

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4
Q

What type of disease is Achrondoplasia?

A

Gain of function, dominant

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5
Q

What type of disease is osteogenesis imperfecta?

A

Loss of function, dominant negative

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6
Q

What are the main clinical symptoms of CF?

A
  • Chronic pulmonary disease
  • Pancreatic exocrine insufficiency
  • Hepatic disease (liver)
  • Intestinal abnormalities
  • Infertility (urogenital abnormalities in males)
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7
Q

Why so much focus on CF?

A

Most common life threatening disease in the UK

1 in 23 carry mutated CFTR gene (>2 million ppl)

Affects over 8000 ppl in the UK

43% of ppl w CF have diabetes

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8
Q

What is the most common mutation in CF?

A

ΔF508

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9
Q

What is ΔF508?

A

3bp deletion –> maintains fram but removes phenylalanine

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10
Q

How many reported mutations are there in the CFTR gene?

A

Over 1000

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11
Q

What is the mutation in PKU?

A

Splice site IVS12+G>A

Or missense = F39L or I65T

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12
Q

What is affected in PKU?

A

The PAH enzyme

Has 21 exons over 80kb

Recessive disease - 2 mutations needed for phenotype

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13
Q

What is the mutation called in ACH?

A

1138G>A

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14
Q

What gene is affected in achondroplasia (ACH)?

A

FGFR3 gene

Occurs at a CpG site (G to A mutation)

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15
Q

What is the amino acid change in ACH?

A

Gly380Arg

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16
Q

What sort of disease is Alpha-thalassamia

A

Loss of function –> recessive

17
Q

What does the muation in Osteogenesis imperfect affect?

A

Collagen production

It is a dominant negative effect

18
Q

What is the genes affected in Osteogenesis imperfecta?

A

COL1A1 & COL1A2

(These code for type 1 procollagen)

19
Q

What is type 1 procollagen?

A

Made up of 3 amino acid chains encoded by COL1A1 and COL1A2

20
Q

What does a null mutation in either COL1A1 or COL1A2 cause?

A

Mild osteogenesis imperfecta

21
Q

What does a missense mutation in either COL1A1 or COL1A2 cause?

A

Severe osteogenesis imperfecta

22
Q

What sort of disease is CMT1A (charcot marie tooth) and PMP22 (pulmonary disease)?

A

Duplication, gain of function, dominant

23
Q

What sort of disease is Haemophillia A?

A

Loss of function, X-linked recessive

24
Q

What type of disease is duchenne muscular dystrophy (DMD)?

A

loss of function, X-linked recessive

25
Q

What type of disease are VCFS and WBS?

A

deltions, loss of function