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Akita

Life expectancy
11.4 years
95% CI 11.1 to 11.6 · McMillan 2024, n=3,828
Highest allele frequency
Cystinuria Type I-A
15% of gene copies · 992 dogs tested · Donner 2023
Behind this page
22 dogs
behind the atlas figures · an early sketch · 992 tested for variants

Akitas have a cited life expectancy of 11.4 years (McMillan 2024 / VetCompass, n=3,828, 95% CI 11.1 to 11.6). The tested variant with the highest allele frequency is Cystinuria Type I-A, at 15% among the 992 Akitas tested (Donner 2023; gene copies, not dogs). 22 dogs stand behind the atlas figures here, so treat this page as an early sketch.

Akita
Photo: Peter Theakston; Keetanii; Melodorakitas; Sevenfatdogs · CC BY 3.0 · Wikimedia

Also known as Akita Inu, Akita Ken, American Akita, and Great Japanese Dog.

Mendelian-disease genetics

Which disease variants turn up in Akitas?

From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), 9 turn up in Akitas at observable frequency. The figure beside each is its allele frequency. Of the gene copies tested in this breed, the share that carry the variant. Every dog carries two copies, so this is not the share of dogs. It is not clinical risk. Most recessive variants require two copies for disease expression; many dominant variants show incomplete penetrance. Read this as a population fingerprint of what's in the gene pool, not a per-dog prediction.

moderate frequency band 15.2%
n = 992 dogs · 3 variants tested · OMIA:000256-9615 · omia.org →
SLC3A1what this gene does

SLC3A1 is a gene that helps transport certain amino acids in the kidneys. It plays a key role in preventing the buildup of cystine, which can form stones.

For your dog: If your dog is from a breed known to carry SLC3A1 variants, it’s worth discussing cystinuria risks with your vet, especially if urinary issues arise.

low frequency band 0.10%
n = 990 dogs · 1 variant tested · OMIA:001432-9615 · omia.org →
RPGRIP1what this gene does

RPGRIP1 is a gene involved in the function of photoreceptor cells in the eye, which help dogs see in different light conditions.

For your dog: If your dog belongs to a breed known to carry RPGRIP1 mutations, it’s worth discussing with your vet to understand the risks and monitor eye health.

n = 987 dogs · 1 variant tested · OMIA:001970-9615 · omia.org →
RAB3GAP1what this gene does

RAB3GAP1 is a gene involved in nerve cell function, particularly in how cells communicate and maintain their structure.

For your dog: If your dog is one of the breeds known to carry this gene variant, it's worth discussing genetic testing with your vet to understand any potential risks.

low frequency band <0.1%
n = 989 dogs · 1 variant tested · OMIA:000157-9615 · omia.org →
FGF4what this gene does

FGF4 influences leg length by affecting bone growth, leading to shorter legs in certain breeds.

For your dog: If your dog is from a breed known to carry this gene, it's worth discussing spinal health with your vet, but being a carrier doesn’t guarantee problems.

low frequency band <0.1%
n = 992 dogs · 1 variant tested · OMIA:001444-9615 · omia.org →
BEST1what this gene does

BEST1 is a gene that helps maintain the health of the retina, the light-sensitive layer at the back of the eye. It plays a role in keeping the cells in the retina functioning properly.

For your dog: If your dog is from a breed known to carry BEST1 variants, it’s worth discussing retinal health with your vet, especially if you notice any vision changes.

Cystinuria Type I-B (SLC7A9 p.A217T)
Autosomal dominant (OMIA); Autosomal recessive (Incomplete penetrance) (Donner 2023)
marker disputed <0.1%
n = 992 dogs · 2 variants tested · OMIA:001880-9615 · omia.org →
SLC7A9what this gene does

SLC7A9 is a gene that helps transport certain amino acids in the kidneys. It plays a role in how the body handles cystine, an amino acid that can form crystals.

For your dog: If your dog is a carrier, it’s worth discussing with your vet to monitor urinary health and catch any issues early.

Dilated Cardiomyopathy risk factor (PDK4-related)
Multifactorial (OMIA); Autosomal dominant (Incomplete penetrance) (Donner 2023)
marker disputed <0.1%
n = 992 dogs · 2 variants tested · OMIA:000162-9615 · omia.org →
PDK4what this gene does

PDK4 helps regulate how cells use energy, especially in the heart muscle.

For your dog: If your dog is one of the breeds known to carry this gene, it’s worth discussing heart health with your vet, but being a carrier doesn’t mean your dog will develop disease.

Hyperuricosuria (HUU)
Autosomal recessive
low frequency band <0.1%
n = 992 dogs · 1 variant tested · OMIA:001033-9615 · omia.org →
SLC2A9what this gene does

SLC2A9 is a gene that helps regulate uric acid levels in a dog's body. It plays a role in how the kidneys handle this substance.

For your dog: If your dog is one of the breeds known to carry this gene variant, it’s worth discussing with your vet to understand any potential urinary health concerns.

low frequency band <0.1%
n = 992 dogs · 1 variant tested · OMIA:001984-9615 · omia.org →
Source: Donner J et al. 2023. Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651 · Evidence: Limited (DTC ascertainment, tag-SNP proxy) · Confounding MEDIUM · License CC-BY-4.0 · Phene IDs from OMIA (Sydney School of Veterinary Science, The University of Sydney; DOI 10.25910/2AMR-PV70).
Sample size in this breed: 992 dogs from the Donner 2023 cohort.
In plain terms

What these results mean for a Akita

About 15 in every 100 copies of this gene in the 992 Akitas tested carry this change (Donner 2023).

  • The kidneys can't hold on to cystine, one of the building blocks of protein. It can form crystals and stones that block the flow of urine.
    OMIA 000256-9615

    “Cystinuria, type 1 - A is an inherited defect that causes failure of reabsorption of cystine in the proximal renal tubule, leading to cystine precipitation in the urine. Formation of crystals and calculi lead to urolithiasis and urinary tract obstruction.” OMIA 000256-9615

What to do
If your dog is straining to pee, or passing little or none, see a vet the same day.

Not tested, or a mix
Without a test, no one can tell how many copies your dog has.

Which Mendelian variants matter most for Akitas?

The Mendelian-disease table above lists nine variants screened in 992 Akitas (Donner 2023). One matters decisively by allele frequency. The rest are vanishingly rare in the breed.

Cone-Rod Dystrophy (cord1-PRA/crd4)

Cone-Rod Dystrophy in Akitas is an autosomal-recessive retinal degeneration with incomplete penetrance. The disease causes progressive vision loss beginning in the cone cells and progressing to the rods. How far it goes varies: some affected dogs keep useful vision late into life.

The cord1-PRA/crd4 variant is rare in Akitas at 0.10% allele frequency (n=990). At that frequency, affected dogs are extraordinarily uncommon. Testing is available, though the low frequency makes it a secondary priority for most breeders.

How should I test my Akita?

For breeding stock, the high-yield test is SLC3A1 (cystinuria Type I-A). It is the most common disease variant in tested Akitas. Cone-rod dystrophy testing is available through the same labs if breeders wish to run a broader panel, but the frequencies are low enough that carrier-to-carrier pairings happen rarely by chance alone.

What does the cystinuria variant mean for an Akita?

The SLC3A1 variant for cystinuria Type I-A is the most common disease variant in tested Akitas, at 15.2% allele frequency (Donner 2023, n=992). The trait is autosomal recessive. A dog needs two copies for the kidneys to lose cystine into the urine, where it can form crystals and stones. A dog with one copy is a carrier and is clinically normal (OMIA 000256-9615).

OMIA’s record for this variant names Bulldogs and Newfoundlands, not Akitas. No study has yet measured how often Akitas with two copies form stones, so this page gives the variant’s frequency and not a rate of disease.

The sign to know: if your dog is straining to pee, or passing little or none, see a vet the same day.

What we don’t know

The published Akita health literature is sparse. No breed-specific survey has documented how often Akitas form cystine stones, or how common other conditions are. The atlas sits at 22 dogs, which is small enough that longevity outliers and sub-population structure cannot be reliably estimated. Life expectancy is 11.4 years (McMillan 2024 / VetCompass, n=3,828); we do not know how closely that UK cohort matches Akitas elsewhere.

Hip dysplasia has been reported anecdotally in the breed, but no breed-club or OFA-aggregated epidemiology is published. Nobody has yet published the data to say whether hip dysplasia is common, rare, or typical for a large breed in Akitas.

Frequently asked questions about Akitas

What is the most common genetic variant in Akitas? The SLC3A1 variant for cystinuria Type I-A. Its allele frequency among tested Akitas is 15.2% (Donner 2023, n=992). Carriers, with one copy, are clinically normal. When two carriers are paired, each puppy has a one-in-four chance of being homozygous-affected. Carrier-by-carrier pairings are avoidable with pre-breeding DNA testing.

Should I do a DNA test on my Akita? For breeding stock, yes. Testing for SLC3A1 (cystinuria) is the high-yield screen and is widely available through commercial DNA labs.

How long do Akitas live? Cited life expectancy is 11.4 years (McMillan 2024 / VetCompass, n=3,828, 95% CI 11.1 to 11.6). Some breed-club surveys suggest slightly longer averages. Large-breed lifespan is variable, and individual dogs often exceed or fall short of these medians.

Are Akitas prone to hip dysplasia? Hip dysplasia is reported anecdotally in the breed, but no published epidemiology exists. Akita breeders are encouraged to have breeding stock hips evaluated by the OFA.

What is the best diet for an Akita? Nothing in the breed’s genetics calls for a special diet for a carrier or a clear dog. A dog with cystine stones is managed by its vet, and diet is part of that plan. Fresh water should always be available.

Can cystinuria in Akitas be managed without surgery? Often, yes. Vets manage cystine stones with diet, more water and medicine that changes the urine, and remove a stone surgically when that fails or a stone blocks the flow. Carriers need no management; they are clinically normal.

Are Akitas good with children? Akitas are large, protective dogs bred historically for guarding. Early socialization and consistent training are essential. Supervision with small children is important given the breed’s size and strength.

What health issues should I watch for in an Akita? Monitor for signs of cystinuria (straining to urinate, blood in urine, abdominal pain) and seek veterinary evaluation if these appear. Hip and elbow screening in breeding stock is recommended. Regular ear cleaning helps prevent infections given the breed’s ear carriage.

Names & origins

Other names

The Akita is also recorded as Akita Inu, Akita Ken, American Akita, Great Japanese Dog, and Japanese Akita.

Identified as Akita (VBO:0200010) in the Vertebrate Breed Ontology (Mullen et al. 2025, CC-BY 4.0) · registry IDs FCI 255 · iDog 4 · VeNom 13638.

For researchers Population genetics, disease models and every recorded condition Open the research detail for the Akita
What the atlas says about Akita

In the atlas, the Akita clusters consistently as Akita (100% of the 22 dogs here). Dogs here sit in a relatively sparse region of the atlas, fewer close neighbors than typical.

Only 22 dogs of this breed in the atlas, modestly sampled.

Genetic dimensions · CanVAS atlas

What the atlas genotypes say about Akita

Computed from the 14,478 CanVAS dogs in the Atlas, on an imputed genotype backbone: 77,215 directly typed sites per dog, imputed to 9.67 million variants.

The confidence below counts dogs, not reads: it is the size of the sample, and it is separate from how the genotypes were measured.

Dogs behind these figures
22Founders
12 from Hayward2016, 10 from Spatola
Genetic diversity
0.29Moderate
Mean heterozygosity across the breed. Its place among 107 ranked populations is not settled: with 22 atlas dogs, resampling them moves it across 40 places.
What does genetic diversity mean?

How varied a breed's gene pool is — the share of gene spots where a typical dog of the breed carries two different versions rather than two identical ones.

How to read it: Higher = more diverse. Among well-sampled breeds it ranges roughly 0.22 (least diverse) to 0.33 (most diverse).

Diversity is a strength, not a verdict on any individual dog. Lower diversity means it's worth paying attention to recessive-risk testing — not that a dog is doomed.

Cluster structure
Single tight cluster
Intra-breed RMS distance: 25.51
What does within-breed variation mean?

How much individual dogs within the breed differ from each other genetically.

How to read it: Higher = more internal variety among individuals of the breed.

Sensitive to how many dogs of the breed we've sampled.

Related breeds
Built from
Distant kin · one shared founding ancestor
In the Working group
Explore the full lineage map →
VBO foundation stock (breeding records) · AKC breed group
Relatedness is documented lineage + kennel family. Genetic-ancestry distance measures diversity, not kinship, so it isn't used here.
How long they live
11.4years (life expectancy)
95% CI 11.1–11.6 · VetCompass, McMillan 2024, n=3,828. source
What does typical lifespan mean?

The median age dogs of the breed tend to reach.

How to read it: Higher = longer-lived. Compare to longevity-for-size to see whether it's just a size effect.

Drawn from population lifespan records; individual dogs vary widely with care, genetics, and luck.

n = 22 dogs · moderate sample · CanVAS (Brundage 2026) · Sniff Atlas
A gift to human medicine

Akitas are a natural model for human disease

Because the same genes cause the same conditions across species, the inherited conditions documented in Akitas help researchers understand, and work toward treating, the human diseases they model. This is the dog advancing human medicine. The breed models the human disease; it does not have it, and this is not a prediction for your dog.

Human equivalents via OMIA → Mondo / OMIM. Model-of, not identity. The named gene is the canine locus, not a claim that a pet has the human disease.
Documented in OMIA

Every condition recorded in the Akita

Beyond the testable carriers above, OMIA's literature catalogue records 4 genetic conditions in the Akita, 3 of which have a known human equivalent. This is the documented landscape across all Akitas ever studied, not a prediction for any one dog.

Online Mendelian Inheritance in Animals (OMIA); Nicholas, Tammen & Sydney Informatics Hub, DOI 10.25910/2AMR-PV70
Documented in the breed's literature is not carrier status and not a forecast for an individual dog. Human equivalents are mapped via Mondo/OMIM. Allele frequencies (above) are the separately-measured testable subset (Donner 2023).
The data behind this page

Where every number on this page came from.

This page draws on three primary data sources. Allele frequencies for the Mendelian section come from Donner et al. 2023 (CC-BY-4.0). We grade these data at evidence Limited because the cohort is a direct-to-consumer ascertainment, which biases toward owners who chose to test their dogs. The panel also uses tag-SNP proxies for some variants rather than direct causal-variant assays. Limited is a study-design grade, not a quality grade: the Donner cohort is the largest open canine-genotype dataset in existence and we are grateful for it. We rate the confounding MEDIUM.

Population-genetic dimensions (heterozygosity, intra-breed PCA distance, nearest neighbors, trait-locus frequencies) come from CanVAS (Brundage 2026), harmonized through the Sniff Atlas. The exact release date and verification commit are pinned at the bottom of the page so a researcher can trace a number back to a specific snapshot. The disease-gene-variant graph comes from OMIA (Online Mendelian Inheritance in Animals; Nicholas, Tammen, and the Sydney Informatics Hub at the Sydney School of Veterinary Science, The University of Sydney; retrieved April 2026, DOI 10.25910/2AMR-PV70).

What this page does not yet have. Inheritance modes and per-disease penetrance evidence from Donner 2023 are in the structured data for every variant the panel covers. Mondo, OMIM, Ensembl, and HGNC cross-references live on the gene and disease pages this page links to, rather than being repeated here. What is still absent from this breed page is anything not in the cited panel, and each such gap carries its cause where it appears.

How to cite this page. The computed dimensions on this page are derived from the open Sniff Atlas v1.0.2 (Gehring 2026, doi:10.5281/zenodo.20566358, CC-BY 4.0). Full citation formats including BibTeX, RIS, and CITATION.cff at sniff.world/cite.

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References
  1. Donner J, Freyer J, Davison S, Anderson H, Blades M, Honkanen L, et al. (2023). Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651. doi:10.1371/journal.pgen.1010651
  2. Brundage DM (2026). CanVAS: A Harmonized and Imputed Canine Variant Atlas. bioRxiv. doi:10.64898/2026.04.13.718238
  3. Nicholas, F.W., Tammen, I., & Sydney Informatics Hub. (2026). Online Mendelian Inheritance in Animals (OMIA) [dataset]. The University of Sydney. https://omia.org. doi:10.25910/2AMR-PV70 (retrieved April 2026).
Last updated
Sources: CanVAS (Brundage 2026) · Donner 2023 · OMIA