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Delta F508/ Delta F508

my65roses4me

New member
<span style=" font-size: x-small;">At birth I was diagnosed with
both Delta F508 genes. I know that there are differences in the
genes that cfers have. Can anyone explain the
differences?<br>
Khristina 31 yr old cfer
 

Emily65Roses

New member
I'm not quite sure what you're asking. But you specifically have the same two CF genes.

Using myself as an example, I do not. I have one DeltaF508 and one called 1898+1G>A. There are more than one thousand different CF genes out there that they're currently aware of.
 

my65roses4me

New member
<span style=" font-size: x-small;">I guess I am asking what
differnet outcomes do cfers have with different genes or is there a
difference. Does one gene make you sicker than others?
 

coltsfan715

New member
I am also not 100% on the question you are asking, but I am thinking you are asking what is the difference between the 2 Delta F508 genes you carry. Is that right?

By my understanding (if that is the question you are asking) there is no difference. You simply have to copies of the same gene mutation. Whereas Emiy has 1 copy of Delta F508 CF gene mutation and 1 copy of CF gene mutation 1898+1G>A.

If you were asking what makes the genes different in general. I think it may be the way that CF presents itself - meaning severity of symptoms, digestive problems involved, pancreatic problems, reproductive problems, respiratory and sinus problems and so on. There are some "less severe" gene mutations that led to the patient presenting few to no symptoms and there are some that led to presenting more symptoms and so on.

Hope one of those answered your question.

Also I don't personally have it but maybe someone will post the list that breaks down the different classes of CF gene mutations - that may answer your question better.

Take Care,
Lindsey
 

coltsfan715

New member
<div class="FTQUOTE"><begin quote>Also, the mutations are classified I-V, here's a summary I found:

Class I mutations lead to defects in the synthesis of stable CFTR mRNA transcripts resulting in absence of the CFTR protein. About half of all mutations in CFTR (encompassing premature termination, exon skipping, aberrant mRNA splicing, and frameshifts) are thought to fall into this class and result in complete loss of CFTR protein/function.

Class II mutations, including F508, complete protein translation but produce an abnormal protein that fails to escape the endoplasmic reticulum. Little or no CFTR reaches the plasma membrane, and the absence of all surface CFTR results in a severe phenotype. It is being increasingly recognized that mutations in unrelated genes can create defective proteins, which fail to traffic properly through the cell. Classically, missense mutations creating an abnormal protein were thought to be relatively benign or less consequential than nonsense mutations (null) or large deletions. This is no longer strictly the case because examples from CF and other inherited disorders demonstrate that a synthesized protein that fails to mature along the normal biosynthetic pathway often becomes quite destructive (7).

Class III mutations disrupt activation and regulation of CFTR at the plasma membrane. Thus biosynthesis, trafficking, and processing are undisturbed, but the channel may be defective with respect to ATP binding and hydrolysis, or phosphorylation. Mutations, such as G551D, tend to be associated with a severe phenotype.

Class IV mutations affect chloride conductance or channel gating and thus result in reduced chloride current. As might be expected, mutations in this class, such as R117H or P574H, are thought to confer a milder phenotype.

Class V mutations reduce the level of normal CFTR protein by alterations in the promoter or by altering splicing. Currently it is thought that a reduction in mRNA to less than 10% of normal results in disease in CF. Examples of Class V mutations include 3849 + 10kb CT, A455E, and 5T.

~Maria (posted as annon)</end quote></div>

That info is from another post I just did a search for, the lady I quoted was not logged in as a site member (but that is the name she signed with).

Hope that was what you were looking for.

Lindsey
 

my65roses4me

New member
<span style=" font-size: x-small;">Yes !! Thank you thats exactly
what I was looking for! Thanks for the info!!<br>
Khristina 31 yr old cfer
 
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