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Cognitive Traits

Discover the Power of Your Mind

These reports provide valuable insights into your genetic predispositions related to cognitive traits such as attention span, memory performance, productivity, and stress response.

Warrior vs Worrier

Night Time Productivity

Dealing with memory Tasks

Caffeine Affecting Focus

Workaholic traits

Attention Span

Reports

Attention Span

Genes of Interest: DTNBP1, COMT, DRD4, BDNF, OXTR

Attention span is a complex trait that is influenced by various genetic and environmental factors. Studies have shown that several genes are involved in regulating attention span, including DTNBP1, COMT, DRD4, BDNF, and OXTR.

DTNBP1 is a gene that codes for dysbindin, a protein that plays a role in regulating neurotransmitter release and synaptic plasticity. Variations in DTNBP1 have been linked to attention deficit hyperactivity disorder (ADHD), a condition characterized by inattention, impulsiveness, and hyperactivity.

COMT is a gene that codes for catechol-O-methyltransferase, an enzyme involved in the breakdown of neurotransmitters such as dopamine and norepinephrine. Variations in COMT have been associated with different levels of neurotransmitter breakdown, which can affect attention span.

DRD4 is a gene that codes for the dopamine D4 receptor, which is involved in regulating the release of dopamine in the brain. Variations in DRD4 have been linked to attention deficit hyperactivity disorder (ADHD) and attention span.

BDNF is a gene that codes for brain-derived neurotrophic factor, a protein that promotes the survival and growth of neurons. Variations in BDNF have been linked to attention deficit hyperactivity disorder (ADHD) and other neurological disorders that can affect attention span.

OXTR is a gene that codes for the oxytocin receptor, which is involved in regulating social behavior and stress response. Variations in OXTR have been linked to attention deficit hyperactivity disorder (ADHD) and other neurological disorders that can affect attention span.

Caffeine Affecting Focus

Genes of Interest: ADORA2A, CYP1A2

The genes ADORA2A and CYP1A2 play a role in how an individual's body processes caffeine, which can in turn affect their focus. ADORA2A is a gene that codes for an adenosine receptor, which is a type of protein that helps regulate the release of certain neurotransmitters like dopamine and norepinephrine. CYP1A2 is a gene that codes for a cytochrome P450 enzyme, which is involved in the metabolism of many different substances, including caffeine.

Studies have shown that variations in these genes can affect an individual's ability to metabolize caffeine and the speed at which they metabolize it. This can result in differences in the effect that caffeine has on an individual's focus. For example, individuals with a slow-acting version of the CYP1A2 gene may experience a greater impact on their focus from consuming caffeine, compared to those with a fast-acting version of the gene.

It's important to note that genetics is only one factor that influences how an individual's body processes caffeine. Other factors such as diet, lifestyle, and overall health can also play a role.

Dealing with memory Tasks

Genes of Interest: ADTNBP1, CHRNA4, DRD2, BDNF

Memory tasks refer to various cognitive activities that require the ability to store, retrieve, and manipulate information. There are several genes that have been found to play a role in how we deal with memory tasks, including DTNBP1, CHRNA4, DRD2, and BDNF.

DTNBP1, also known as dysbindin, is a gene that has been linked to memory performance, especially in individuals with a history of psychiatric disorders. A study published in the Journal of Psychiatric Research found that carriers of a specific DTNBP1 variant had lower working memory capacity compared to non-carriers.

CHRNA4 is a gene that encodes the alpha-4 subunit of the nicotinic acetylcholine receptor, a type of neurotransmitter receptor that is involved in various cognitive processes, including memory formation and recall. A study published in the Journal of Alzheimer's Disease found that carriers of a specific CHRNA4 variant had poorer performance on memory tests compared to non-carriers.

DRD2 is a gene that encodes the dopamine D2 receptor, which is involved in regulating the release of dopamine in the brain. Dopamine is a neurotransmitter that plays a role in motivation, reinforcement, and reward-seeking behavior, as well as in the regulation of learning and memory processes. A study published in the Journal of Neural Transmission found that carriers of a specific DRD2 variant had lower memory performance compared to non-carriers.

BDNF, or brain-derived neurotrophic factor, is a protein that is involved in the growth and survival of neurons, as well as in the regulation of synaptic plasticity and memory formation. A study published in the Journal of Neurochemistry found that carriers of a specific BDNF variant had lower memory performance compared to non-carriers.

Night Time Productivity

Genes of Interest: AANAT, CRY1, PER3, COMT

The genes AANAT, CRY1, PER3, and COMT have been linked to cognitive abilities during nighttime tasks. The gene AANAT, which encodes for the enzyme arylalkylamine N-acetyltransferase, is involved in regulating the circadian rhythm, which helps dictate the sleep-wake cycle. A variation in the AANAT gene has been shown to affect the timing of the circadian rhythm and sleep quality.

The gene CRY1 encodes for the protein cryptochrome 1, which is also involved in regulating the circadian rhythm. A study found that individuals with a variation in the CRY1 gene had altered sleep patterns and decreased cognitive ability during nighttime tasks.

The gene PER3 encodes for the protein period 3, which is a component of the circadian rhythm-regulating machinery in the brain. Variations in the PER3 gene have been associated with decreased cognitive ability during nighttime tasks and sleep disturbances.

The gene COMT encodes for the catechol-O-methyltransferase enzyme, which is involved in the degradation of neurotransmitters such as dopamine and norepinephrine. Studies have shown that variations in the COMT gene can affect cognitive abilities, including working memory, especially during nighttime tasks.

In conclusion, the genes AANAT, CRY1, PER3, and COMT play important roles in regulating the circadian rhythm and neurotransmitter degradation, which can impact cognitive ability during nighttime tasks. However, more research is needed to fully understand the interactions between these genes and their effects on cognitive function.

Warrior vs Worrier

Genes of Interest: COMT

The gene COMT plays a role in our response to stress, specifically in whether we tend to worry or fight during stressful situations. This gene encodes for the catechol-O-methyltransferase enzyme, which is involved in the breakdown of neurotransmitters such as dopamine, norepinephrine, and epinephrine.

Variants in the COMT gene can affect the activity of the enzyme, leading to different levels of neurotransmitter breakdown. Those with the "worrier" allele tend to have lower activity of the COMT enzyme, leading to higher levels of neurotransmitters in the brain. This can result in a more anxious and fearful response to stress. On the other hand, those with the "warrior" allele tend to have higher activity of the COMT enzyme, leading to lower levels of neurotransmitters and a more proactive, problem-solving response to stress.

It's important to note that genetics is just one factor influencing our response to stress and that our environment, life experiences, and other genetic factors also play a role. Additionally, while research has shown a correlation between certain COMT variants and stress response, it is not a definitive predictor of behavior.

Workaholic traits

Genes of Interest: SLC6A4, COMT, TPH2

The genes SLC6A4, COMT, and TPH2 are thought to play a role in regulating workaholic traits. The SLC6A4 gene, also known as the serotonin transporter gene, is involved in the regulation of serotonin levels in the brain. Serotonin is a neurotransmitter that is believed to play a role in regulating mood, motivation, and stress response. Some studies have found a link between the SLC6A4 gene and higher levels of workaholism, suggesting that people with certain variants of the gene may be more prone to working excessively.

COMT, or catechol-O-methyltransferase, is a gene that helps to break down neurotransmitters like dopamine, norepinephrine, and epinephrine. Variations in the COMT gene have been linked to differences in cognitive ability, including executive function and decision making. Some research has suggested that people with certain variants of the COMT gene may be more prone to workaholism, as they may have a greater ability to focus and are less easily distracted.

TPH2, or tryptophan hydroxylase 2, is a gene that helps to produce serotonin. Variations in the TPH2 gene have been linked to differences in serotonin levels in the brain, which can impact mood and behavior. Some studies have suggested that people with certain variants of the TPH2 gene may be more prone to workaholism, as they may have a greater need for achievement and may be less likely to feel satisfied with their work.

Overall, the relationship between genes and workaholic traits is complex and not fully understood. However, research into these genes has provided some insight into the biological factors that may contribute to a tendency towards excessive work.

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