Studies have found ~10–20% of human genes are orphans.
Some are tied to distinctly human traits, such as brain development and speech.
Example: SRGAP2C is a gene copy unique to humans that influences brain neuron development. It’s not present in chimps or gorillas, yet it plays a role in the very thing that makes us “human.”
Evolutionary Problem: if humans only split from chimps a few million years ago, where did these entirely new genes come from in such a short time?
In fruit flies, ~12–15% of the genes are orphans.
What makes it worse: many orphan genes in flies are essential for survival.
Example: some orphans regulate embryonic development and fertility.
Evolutionary Problem: how could essential, never-before-seen genes just appear by chance without precursors?
Yeast genomes contain hundreds of orphan genes.
Several are linked to stress response and survival under harsh conditions.
Evolutionary Problem: yeast supposedly evolved slowly over billions of years — but these unique, functional genes appear with no ancestry.
In some plants (like rice), up to 40% of the genes are orphans.
Many regulate flowering, photosynthesis, and adaptation to environment.
Evolutionary Problem: nearly half a plant’s genome with no detectable relatives? That doesn’t look like “gradual modification” — it looks like new information injected.
Octopuses have a ton of orphan genes (hundreds). Many are tied to their unique nervous system and camouflage.
Kangaroo rats and other mammals also show dozens of lineage-specific orphans.
These often align with unique adaptations that distinguish the species.
Sheer Volume: up to 40% in some organisms (plants).
Essential Functions: many orphan genes aren’t just extras — they’re crucial to survival and uniqueness of the species.
No Precursors: no evolutionary trail of “broken” or “half-built” versions leading up to them.
Timing: many appear in relatively recent lineages (humans, flies), when evolution shouldn’t have had much time to invent totally new genes.
Plants → Fungi, Fungi → Plants
Some plants carry genes that appear to come from fungi, and vice versa.
Example: genes for digesting cellulose and detoxifying soil compounds.
Problem: morphologically, these groups are incredibly distant, with no plausible shared ancestor recently enough to account for it.
Aphids (tiny insects) have carotenoid-producing genes that don’t exist in other insects — they’re bacterial.
Carotenoids are pigments usually made by plants, fungi, or bacteria.
No evolutionary “bridge” insect lineages exist.
Looks like the aphids just leapfrogged time and lineage, acquiring a complex biochemical pathway wholesale.
Segments of viral DNA are embedded in mammalian genomes.
Evolutionists claim they “prove common ancestry” when shared.
But: sometimes ERV insertions appear in species that supposedly diverged long before the virus existed.
In other words, the “descendant” species seems to have the viral DNA before the virus is thought to have appeared.
This is usually hand-waved as “independent insertions” — but that strains probability.
Certain sea slugs (e.g., Elysia chlorotica) can photosynthesize because they contain genes from algae.
These photosynthesis-related genes don’t exist in other mollusks.
Problem: The gene transfer requires not just one enzyme but an entire suite of machinery, which seems to have “skipped” millions of years of divergence and morphological constraints.
Some HGT cases create what’s called time paradoxes: genes appear in species that, according to the fossil record and evolutionary tree, branched off before the gene supposedly evolved.
Example:
Certain metabolic genes in microbes appear in ancient lineages that should not have had them yet, if the standard tree is correct.
To fix this, scientists often propose multiple independent origins (unlikely) or HGT “backwards in time.”
Morphological Defiance: Genes appear in organisms that show no physical or developmental pathway to having them.
Time Defiance: Genes show up “too early” — before the ancestor that supposedly evolved them.
Tree Collapse: Instead of a clean lineage, you get a messy web that looks more like code being patched in across unrelated platforms.
Mammals separated by ~50 million years and vastly different morphologies.
Both evolved echolocation systems involving:
Specialized larynx/nose structures (bats) or nasal sacs (dolphins).
Unique ear structures tuned to ultrasonic frequencies.
Brain regions dedicated to sonar processing.
Identical mutations in the Prestin gene (linked to high-frequency hearing).
So it’s not just “similar function” — it’s convergent morphology + neurobiology + genetics.
Squids and octopuses vs. mammals/birds.
Eyes evolved “independently” with:
Cornea, lens, iris, retina.
Complex neural circuitry.
Even shared developmental genes (Pax6) turning on eye formation.
These groups are separated by ~500 million years and radically different body plans.
The “camera eye” supposedly evolved twice — with massive interdependent systems.
Evolved independently in at least six lineages of fish (e.g., electric eels, rays, catfish).
Requires:
Muscle cells transformed into electrocytes.
Complex ion channel arrangements.
Neural control systems.
And yet they all ended up with similar functional systems for shock and navigation.
Four separate groups, separated by hundreds of millions of years.
Each evolved:
Lightweight skeletal adaptations.
Aerodynamically functional wings.
Complex muscle and metabolic adaptations.
Neural systems for flight control.
These are deeply integrated systems, not one-off traits.
Venoms evolved multiple times independently in snakes, spiders, cone snails, jellyfish, and even some mammals (like shrews).
Requires:
Specialized glands.
Delivery systems (fangs, stingers, spines).
Complex biochemical cocktails of toxins.
Convergence here means whole biochemistry pathways emerged multiple times.
Appeared independently in:
Saber-toothed cats (true felids).
Thylacosmilus (a marsupial predator).
Even in some earlier synapsids.
All had the same suite of adaptations: elongated canines, jaw mechanics, neck muscles.
Morphologically and temporally distant, yet “the same design” shows up repeatedly.
Multi-system convergence: It’s not just one trait, but clusters of interdependent systems evolving “by chance” multiple times.
Morphological gulf: These organisms are separated by massive differences in form, ancestry, and ecology.
Genetic convergence: Sometimes even the same genes or mutations are reused (like Prestin in bats/dolphins), which is extremely unlikely under random mutation.
Time separation: Many convergences occur across tens or even hundreds of millions of years.
“Convergent evolution doesn’t just explain one-off traits. It claims bats and dolphins independently evolved sonar, squids and humans independently evolved camera eyes, and fish invented electric organs six times. That’s multiple interdependent systems — morphologically and genetically — converging across vast gulfs of time. That looks a lot less like blind trial and error, and a lot more like common design.”
Traits don’t just evolve, vanish, and stay gone… in many cases they supposedly evolve, disappear completely, and then re-evolve again later in unrelated lineages. Evolutionary biologists call this “trait re-evolution” or “character reversal.”
Here are some of the most eyebrow-raising cases:
Most frogs lost teeth on the lower jaw over 200 million years ago.
But one species (Gastrotheca guentheri) mysteriously has them again.
That means the trait supposedly went extinct in the entire frog lineage… then re-evolved in a single branch.
Birds lost teeth ~100 million years ago, evolving beaks instead.
But experiments show that bird embryos still retain suppressed genetic pathways that can make teeth.
This suggests the trait was “lost” then partially reactivated — a case of re-evolution buried in their genome.
Wingless stick insects (Phasmatodea) supposedly lost wings, then later re-evolved fully functional wings in multiple lineages.
A 2011 Nature paper even titled its finding: “Resurrection of a lost trait in stick insects.”
Problem: wings are extremely complex, requiring dozens of integrated traits.
Some lizards that evolved limblessness (like snakes) show partial re-evolution of limbs in certain fossil lineages.
Example: Bipes (a mole lizard) has forelimbs but no hindlimbs, suggesting reversal of limb loss.
Axolotls also show “atavistic” limb structures under certain conditions.
Some extinct turtle lineages lost shells, only to re-develop them later.
A re-emergence of a highly complex, integrated structure after its disappearance.
Eyes, shells, and even flight have supposedly been “lost” and “regained” multiple times in different lineages.
Example: Certain cavefish lost eyes, and related lineages re-evolved them when re-exposed to light environments.
Dollo’s Law (longstanding evolutionary principle): Once a complex trait is lost, it cannot be regained.
Yet these cases repeatedly violate Dollo’s Law.
Extreme Improbability: The odds of rebuilding a multi-part system (like wings, teeth, or eyes) from scratch are astronomically small.
Genetic “Resurrection”: Sometimes it’s argued the genetic pathways were “kept dormant” — but why would useless genetic material be preserved for millions of years without being eliminated by mutation and drift?
Design Angle: Much easier explained if organisms are designed with flexible/deployable genetic toolkits that can activate or deactivate traits when needed.
“Evolutionists once held Dollo’s Law: complex traits don’t re-evolve once lost. But frogs supposedly lost teeth for 200 million years — then grew them again. Wingless stick insects re-evolved wings. Birds lost teeth, but embryonic birds still show the capacity to regrow them. This isn’t random trial and error — it looks like latent design blueprints being switched on and off.”