Morph breeding · July 5, 2026 · 8 min read

Morph odds without the hand-waving

Recessive, co-dominant, incomplete dominant, polygenic and line-bred traits behave differently in a pairing. Here is how each one is inherited and where breeders most often get the maths wrong.

Pairing decisions get made on odds, and the odds get quoted wrong constantly. The categories matter because each one produces a completely different clutch distribution.

Recessive traits

Two copies are needed for the animal to look different. Visual × visual gives all visuals. Visual × het gives half visual, half het. Het × het gives one in four visual — and, importantly, two thirds of the normal-looking siblings are hets, which is where '66% het' comes from.

'100% het' means proven by parentage. '50% het' is a probability, not a description of the animal. Sell it labelled honestly, and note that only breeding or genetic testing converts a possible het into a known one.

Co-dominant and incomplete dominant traits

One copy shows, two copies show differently — the 'super' form. A single-gene animal bred to a normal gives half single-gene, half normal. Two single-gene animals give one super, two single-gene, one normal.

This is where the super form matters most: in some lines the super is a lethal or severely compromised animal, and the pairing is a decision about welfare, not just about odds. Know what the super of your gene does before you set the pairing.

Dominant traits

One copy shows and a second copy adds nothing visible, so a dominant animal bred to a normal produces roughly half showing the trait. Because the super is indistinguishable, you cannot tell a homozygous animal from a heterozygous one by looking.

Polygenic and line-bred traits

Structure, pattern quality, white coverage in many crested gecko lines, colour saturation — these are not single genes. They respond to selection over generations, not to a Punnett square, and they are heavily influenced by husbandry and age.

A common and costly mistake is treating a line-bred appearance as if it were a simple dominant gene. Buying a 'high white' animal does not buy you a gene; it buys you a place in someone's selection programme, which you then have to continue.

Where the maths goes wrong

  • Averaging odds across a clutch. Every egg is an independent roll — a four-egg clutch at 25% odds very often produces zero hits.
  • Stacking traits without multiplying. Two independent 1-in-4 outcomes together is 1 in 16, not 1 in 8.
  • Ignoring known lethal or deleterious super combinations.
  • Compounding relatedness. Odds say nothing about inbreeding; track a coefficient of inbreeding separately and set a ceiling you will not cross.

Next steps

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