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“Cait”
Nuphar's Connect The Dots NJK JW'16 W'16 BJS'16 EJS'17 DEJK BNLW NL'17 BNLW L'17 BS'17

Barbet

“Outdoors Asterix x MBIS BISS MCh. Nuphar's Deep In A Dream. Hips FCI A. Eyes ECVO clear (17/2/2017).”

This dog has been viewed 162 times and been given 0 wags

Registration

NHSB: 3030599

Genetic Breed Result

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Barbet

Barbet Barbet
A native of France, this agile, wooly sporting dog is fun-loving and smart. They were bred for retrieving waterfowl and even have webbed feet to help with their swimming.
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Genetic Stats

Predicted Adult Weight: 30 lbs Learn More
Genetic Age: 33 human years Learn More

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Health

Traits

Maternal Haplotype

Paternal Haplotype

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Summary

0
AT RISK
0
CARRIER
165
CLEAR
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Clinical Traits

These clinical traits are valuable to your veterinarian and can inform the clinical decisions and diagnoses they make.

Alanine Aminotransferase (ALT) Activity result: Low Normal

Nuphar's Connect The Dots has two copies of a mutation associated with reduced ALT activity. Please inform your veterinarian that Nuphar's Connect The Dots has this genotype, as ALT is often used as an indicator of liver health and Nuphar's Connect The Dots is likely to have a lower than average resting ALT activity. As such, an increase in Nuphar's Connect The Dots’s ALT activity could be evidence of liver damage, even if it is within normal limits by standard ALT reference ranges.

Genetic Health Conditions

A genetic health condition indicates a genetic mutation that increases the risk that an animal develops a specific disease.

Not At Risk

Good news! Cait did not test positive for any of the genetic diseases that Embark screens for.

It is still important to let your veterinarian know these results because they could help guide Cait’s diagnosis and treatment if she gets sick in the future.

Not A Carrier

Good news! Cait is not a carrier for any of the genetic diseases that Embark tests for.

Common Conditions

Good news! Cait tested clear for 1 genetic conditions that are common in her breed.
Condition List

Progressive Retinal Atrophy - prcd
Progressive rod-cone degeneration (PRCD Exon 1)
Eyes

This retinal disease causes progressive, non-painful vision loss. The retina contains the cells, photoreceptors, that collect information about light: that is, they are t…

Other Conditions:
Clear of 164

Cait is clear of 164 other genetic diseases that Embark tests for.

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Traits

Maternal Haplotype

Paternal Haplotype

Explore the genetics behind your dog’s appearance, size, and genetic diversity.

Coat Color

E Locus (MC1R)
No dark mask or grizzle (Ee)
K Locus (CBD103)
More likely to have a mostly solid black or brown coat (KBKB)
A Locus (ASIP)
Not expressed (aya)
D Locus (MLPH)
Dark areas of hair and skin are not lightened (DD)
B Locus (TYRP1)
Black or gray hair and skin (Bb)

Other Coat Traits

Furnishings (RSPO2) LINKAGE
Likely furnished (mustache, beard, and/or eyebrows) (FF)
Coat Length (FGF5)
Likely long coat (TT)
Shedding (MC5R)
Likely light shedding (CC)
Coat Texture (KRT71)
Likely curly coat (TT)
Hairlessness (FOXI3) LINKAGE
Very unlikely to be hairless (NN)
Oculocutaneous Albinism Type 2 (SLC45A2) LINKAGE
Likely not albino (NN)

Other Body Features

Muzzle Length (BMP3)
Likely medium or long muzzle (CC)
Tail Length (T)
Likely normal-length tail (CC)
Hind Dewclaws (LMBR1)
Unlikely to have hind dew claws (CC)
Blue Eye Color (ALX4) LINKAGE
Less likely to have blue eyes (NN)

Body Size

Body Size (IGF1)
Smaller (II)
Body Size (IGFR1)
Larger (GG)
Body Size (STC2)
Intermediate (TA)
Body Size (GHR - E195K)
Larger (GG)
Body Size (GHR - P177L)
Larger (CC)

Performance

Altitude Adaptation (EPAS1)
Normal altitude tolerance (GG)

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Health

Maternal Haplotype

Paternal Haplotype

Through Cait’s mitochondrial DNA we can trace her mother’s ancestry back to where dogs and people first became friends. This map helps you visualize the routes that her ancestors took to your home. Their story is described below the map.

Haplogroup

C2

Haplotype

C3/14

Map

C2

Nuphar's Connect The Dots’s Haplogroup

C2 is a very old female lineage found more commonly among English Setters, English Bulldogs, and American Eskimo Dogs. We also see C2 in village dogs in South Asia. Rather than having a few characteristic breeds representing this lineage particularly well, it is present in a few uncommon individuals of many different breeds. Unlike some European breed lineages that have seen skyrocketing popularity along the path to the modern dogs we see today, C2 tends to reflect the deep history of man's best friend.

C3/14

Nuphar's Connect The Dots’s Haplotype

Part of the C2 haplogroup, this common haplotype occurs most often in English Setters, Cairn Terriers, Labrador Retrievers, and village dogs in Peru, Fiji, and across Africa.

Some other Embark dogs with this haplotype:

You can often find his haplogroup in the lovable English Bulldog.

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Health

Traits

Paternal Haplotype

This 'Paternal Haplotype' tab is for deep ancestral lineage going back thousands of years.

For recent ancestry—"What breeds did my dog inherit from her mom and dad?"—please refer to the Breed, Family Tree, or Summary tab.

The Paternal Haplotype refers to a dog’s deep ancestral lineage stretching back thousands of years, before there were any distinct breeds of dog. We determine the Paternal Haplotype by looking at a dog’s Y-chromosome—but not all dogs have Y-chromosomes!

Why can’t we show Paternal Haplotype results for female dogs?

All dogs have two sex chromosomes. Female dogs have two X-chromosomes (XX) and male dogs have one X-chromosome and one Y-chromosome (XY). When having offspring, female (XX) dogs always pass an X-chromosome to their puppy. Male (XY) dogs can pass either an X or a Y-chromosome—if the puppy receives an X-chromosome from its father then it will be a female (XX) puppy and if it receives a Y-chromosome then it will be a male (XY) puppy. As you can see, Y-chromosomes are passed down from a male dog only to its male offspring.

Since Cait is a female (XX) dog, she has no Y-chromosome for us to analyze and determine a paternal haplotype.

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Health

Traits

Maternal Haplotype