HerpZillA said:
Ok, this is the first I have heard of the diffusion portion being proven to 1 locus.
Yep, this is where all the pewters, granites, fires, plasmas, avalanches, whiteouts, cow plops :grin01: , etc etc come from.
As for co dom/incomplete dom,, I have a good friend that ALWAYS tells me there are no co dom, in corns the way there are in boas or pythons.
There are, I'm sure. They have tens of thousands of genes.
I think the reason we don't have a pile of them yet is because of the way they are discovered. In corns we are working with a mostly closed population and finding things through inbreeding, which will bring recessive genes to the surface. The way we'd find a dominant or codominant gene is to have a spontaneous mutation occur within the captive population.
In boas/pythons they seem to be discovering new genes by simply mass-importing thousands of specimens, or at least by picking through thousands (or tens of thousands?) of WC specimens. Obviously the only thing you're going to find is something that is het for a codominant or dominant mutant, or something that's homo for a recessive mutant. Then if it's a non-recessive on/off gene, all it takes is one breeding to make a good case that it's heritable (half the clutch is mutants, the other half is normal) and you've got a new "proven" gene. (I find it interesting though that they don't then go about breeding them to each other to determine if it's codominant or fully dominant... they finally figured that out with motley in boas after something like ten years... ?)
In corns the closest we have is diffusion. It's still a possibility that caramel, lavender, and hypo are not as completely recessive as we think. And I'm not convinced that motley always has zero effect in hets. But these are a far cry from salmon, pastel, etc.
