The child since they don't inherit
dddd (they only get dd)
unless we are talking two genes
one gene = 1:8 chance of recessiveness
Two genes = 1:16
look at "V. Studying Two Traits at once: (Dihybrid Cross) " on this page
http://www.biology.iupui.edu/biocourses/N100/2k4ch10genetics.html

in which case the nomenclature is AaBb

The problem is that this can't be directly extrapolated to a population.... 
punnett squares only work when you consider only the parents and the offspring.

On the other hand, I wouldn't go with a mendelian inheritance scheme at all. 
I'd probably decide to go with an Alzheimer's type  pattern in which it seems 
that multiple copies of a specific portion of a gene (copies of a motif) lead 
to an increase in how early in life you get the disease. So for magery I'd say 
X copies = magery 1, Y copies = magery 2, and Z copies = magery 3.
So most people have 2 copies and no magery. But rare people have 4 copies (2 on 
each chromosome) and those get magery 1, or occasionally a duplication will 
arise randomly and a person will have 2 copies on one chromosome and one on the 
other.... which =no magery. But if that person marries a mage level 1 then they 
have a 1:2 chance of having a mage child. If a mage level 1 marries a mage 
level 1 then their childern are mage level one, but there is again a chance of 
duplication which would result in a 1:2 chance of having a mage level 2 
child....

The chance of duplication is really really low and you can always declare a 
higher number of copies to get magery 1 - (One form of inheritable Alzheimers 
that doesn't show an effect until you have 20+ repeats of a CAG motif in your 
genetics)... this means it's a really really low percentage of the population 
that gets Alzheimers from this change.
That way you can have a rare trait that becomes more intense if two people with 
the same trait get together... and yet it still stays rare with in the 
population.

-Sue

----- Original Message ----
From: "[EMAIL PROTECTED]" <[EMAIL PROTECTED]>
To: The GURPSnet mailing list <[email protected]>
Sent: Monday, April 30, 2007 12:01:36 PM
Subject: Re: [gurps] Fake scientific genetics for Magery...


At 09:59 AM 4/30/2007 -0700, you wrote:
>[EMAIL PROTECTED] wrote:
>> Ok, after seeing some of the comments made thus far - the question I have
>> is, were my numbers more or less on the money, and if so, does it make for
>> a reasonable explanation?
>
>No, your numbers were not on the money. You're making the assumption 
>that there's a 50% chance of having each of the specific genes, and the 
>real chance can range anywhere from 0 to 100%, depending mostly on 
>evolutionary advantage.
>
>If you want to have a constant low rate of a trait, it implies that 
>either the trait is not significantly evolutionarily favored (seems 
>unlikely for magery) or that the trait is one which results in 
>evolutionary disadvantages if it becomes too prevalent in the breeding 
>pool (e.g. the gene for sickle-cell anemia gives resistance to malaria 
>if you have one copy, but is likely to kill you if you have two copies).
>
>A dominant gene that produces negative effects if it occurs twice is 
>pretty easy to recognize, however, and would just mean that mages always 
>breed with non-mages. Some combination of multiple genes is probably 
>more reasonable.


Ok, in saying I was off the mark, you made me re-evaluate what my
assumptions where rather than plot them out.  A simple Dominant/Recessive
trait scheme would result in the following mendel square:

Mother: DD
Mother: dD
Mother: Dd
MOther: dd

Father: DD
Father: Dd
Father: dD
Father: dd

The odds of having the traits required where the child born has both dd is
actually 1 in 4, rather than 1 in 2.  I used the reciprocal of 2^n where n
= number of gene sites required to produce a magery of a given level.

The actual odds of achieving a given trait where both are recessive depends
on both parents giving the child the recessive gene.  When you increase the
number of gene sites to 2, the odds of a child getting recessives at both
sites becomes 1 in 16.

Which means, that instead of the formula being the reciprocal of 2^N where
N = number of genes involved, it looks like I should have used the
reciprocal of 4^N where N = number of sites.

Can anyone confirm?
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