As one whom teaches genetics, why do we say the inheritance of hypomelanism is codominant? Codominant inheritance results in the equal expression of both alleles at the molecular level which in turn is usually expressed phenotypically, such as in blood types (e.g. AB, Ai, Bi). From the literature I have read, hypomelanism in Boa constrictors (to date) is referred to as incomplete dominance. Incomplete dominance is not as extreme as codominance, in that the phenotypic expression lay somewhere between the wild type (normal) and the mutant. I believe for our hobby/industry(breeding) to receive respect and recognition, we should clear up the language we use to describe what we do (if you are a morpher). Minimally, hypos should be described as being the result of incomplete dominance due to the array of hypos out there (i.e. evidenced by the varying degree of hypomelanism in said animals). At most, we should simply say hypomelanism is a dominant trait.
Here are some problems people will have with hypomelanism being a dominant trait: in dominance-based inheritance, the heterozygote is normally indistinguishable from the wild type and would have to go through a test cross to identify its genetics. Furthermore, how do we definitively distinguish between heterozygote and homozygote mutants (aside from the cleaner and more aberrant hypos, which does not always work out).
The hypo thing is a bit of an anomaly, but until it is fully understood (i.e. the molecular basis of the mutation) I feel it is better to say the mutation is incompletely dominant or simply dominant (with revision).
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Ron Michelotti
Class Reptilia
www.classreptilia.com

)To be honest,I think based on your information,the Salmon/Orange-tail mutation would best fit the definition of dominant,for the exact reasons you explained.I feel certain that someone with a level of experience breeding,and,assessing several hundreds of individuals over the course of time,could probably achieve the percentage level of 90/95%(like Rich,for example.) in accurately determining homozygous from heterozygous expression,maybe even higher? I also think that if I were able to view an entire litter containing both hets,and,"supers",I could probably score fairly high as well?(probably not 90% though?) however,the simple definition,for the sake of discussion,would be that with a "dominant" mutation,both heterozygous,and,homozygous forms look the same,this is why we say "possible super" in presenting an animal for sale from parents that also express the trait.(this may have been less true in the begining,but,at this stage of their production,there are an increasing number of "F1" hets,that lack melanin below the vent,and,exhibit extreme pattern reduction,(two of the primary visual ques used to differentiate between the two.)making it difficult for the average person to tell them apart with any real degree of certainty.)Something like what is currently being seen with the Jungle mutation,comes much closer to the simple definition of "co-dominant",(at least the way we are using it?)in that,the heterozygous form looks different from WT,but het,and,homozygous are dissimilar in appearence? without delving into the molecular,wouldn't the simplest,and,most straightforward definitions serve our interests best?(I'm just asking,*lol* I'm not trying to change the world here!
snip) I've seen numerous homozygotes that appeared less intensely expressive than many hets,so the fact that it can present any doubt at all in discerning between the two represents reasonable reconsideration to my way of thinking?