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Millie

Boykin Spaniel

“Millie is 110% enthusiastic about every second of every day. She is a blast to be with and brings so much sweetness, life, and joy to our family. She is an incredible swimmer and great waterfowl retriever and upland flusher. We got her as a puppy as a hunting companion from Upstate Gun Dogs in Abbeville, SC.”

Place of Birth

Abbeville, SC, USA

Current Location

Athens, Georgia, USA

From

Abbeville, SC, USA

This dog has been viewed and been given 7 wags

Genetic Breed Result

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Boykin Spaniel

The Boykin Spaniel is a compact hunter that hails from South Carolina. This is a relatively new breed that excels at retrieving on land and in water. These guys are very intelligent and compassionate, and they make wonderful pets.

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Here’s what Millie’s family tree may have looked like.
While there may be other possible configurations of her family’s relationships, this is the most likely family tree to explain Millie’s breed mix.
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Health Summary

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Millie is at increased risk for one genetic health condition.

And inherited one variant that you should learn more about.

Intervertebral Disc Disease (Type I)

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Millie inherited both copies of the variant we tested

What does this result mean?

Our research indicates that this genetic variant is likely to increase the risk that Millie will develop this disease.

Scientific Basis

Research studies for this variant have been based on dogs of other breeds. While dogs with similar breeds to Millie have not yet been the focus of research studies, our data indicates that Millie is likely to be at increased risk.

What is Intervertebral Disc Disease (Type I)?

Type I Intervertebral Disc Disease (IVDD) is a back/spine issue that refers to a health condition affecting the discs that act as cushions between vertebrae. With Type I IVDD, affected dogs can have a disc event where it ruptures or herniates towards the spinal cord. This pressure on the spinal cord causes neurologic signs which can range from a wobbly gait to impairment of movement. Chondrodystrophy (CDDY) refers to the relative proportion between a dog’s legs and body, wherein the legs are shorter and the body longer. There are multiple different variants that can cause a markedly chondrodystrophic appearance as observed in Dachshunds and Corgis. However, this particular variant is the only one known to also increase the risk for IVDD.

Collie Eye Anomaly

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Millie inherited one copy of the variant we tested

What does this result mean?

This variant should not impact Millie’s health. This variant is inherited in an autosomal recessive manner, meaning that a dog needs two copies of the variant to show signs of this condition. Millie is unlikely to develop this condition due to this variant because she only has one copy of the variant.

What is Collie Eye Anomaly?

Named for its high prevalence in Collie dogs, Collie Eye Anomaly (CEA) is more correctly termed choroidal hypoplasia. The choroid anchors the retina to the underlying structures and supplies it with oxygen and nourishment. CEA is a developmental disease of the choroid.

Breed-Relevant Genetic Conditions

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Progressive Retinal Atrophy, prcd

Identified in Boykin Spaniels

Progressive Retinal Atrophy, crd4/cord1

Identified in Boykin Spaniels

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency

Identified in Boykin Spaniels

Degenerative Myelopathy, DM

Identified in Boykin Spaniels

Exercise-Induced Collapse, EIC

Identified in Boykin Spaniels

Additional Genetic Conditions

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Traits

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

Base Coat Color

Base Coat Color

Coat Color Modifiers

Coat Color Modifiers

Other Coat Traits

Other Coat Traits

Other Body Features

Other Body Features

Body Size

Body Size

Performance

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Through Millie’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

A1b

Haplotype

A414/643

Map

A1b

Millie’s Haplogroup

This female lineage was very likely one of the original lineages in the wolves that were first domesticated into dogs in Central Asia about 15,000 years ago. Since then, the lineage has been very successful and travelled the globe! Dogs from this group are found in ancient Bronze Age fossils in the Middle East and southern Europe. By the end of the Bronze Age, it became exceedingly common in Europe. These dogs later became many of the dogs that started some of today's most popular breeds, like German Shepherds, Pugs, Whippets, English Sheepdogs and Miniature Schnauzers. During the period of European colonization, the lineage became even more widespread as European dogs followed their owners to far-flung places like South America and Oceania. It's now found in many popular breeds as well as village dogs across the world!

A414/643

Millie’s Haplotype

Part of the A1b haplogroup, this haplotype occurs most frequently in the English Springer Spaniels.

A1b is the most common haplogroup found in German Shepherds.

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The Paternal Haplotype reveals a dog’s deep ancestral lineage, stretching back thousands of years to the original domestication of dogs.

Are you looking for information on the breeds that Millie inherited from her mom and dad? Check out her breed breakdown and family tree.

Paternal Haplotype is determined 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 Millie is a female (XX) dog, she has no Y-chromosome for us to analyze and determine a paternal haplotype.

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