Evidence map›Paper›PMID 41701742›Full record

ArticlePloS one2026

Identification of SORCS1 as a candidate gene associated with canine behavioral traits: Insights from guide dog training outcomes.

Toshinori Omi, Chihiro Udagawa, Yuiko Kato, Shota Kawakami, Yumiko Uno, Kazuhiko Ochiai, Junzo Asano

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Toshinori OmiDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9303-2746
Chihiro UdagawaDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.
Yuiko KatoDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.
Shota KawakamiDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.
Yumiko UnoDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2857-130X
Kazuhiko OchiaiDepartment of Veterinary Hygiene, Nippon Veterinary and Life Science University, Tokyo, Japan.
Junzo AsanoDepartment of Basic Science, Nippon Veterinary and Life Science University, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although genetic factors contribute to behavioral variation in working dogs, the underlying molecular determinants remain poorly understood. The sortilin-related VPS10 domain-containing receptor 1 (SORCS1) gene is highly expressed in the central nervous system and has been implicated in neuronal signaling and synaptic regulation. A preliminary genome-wide association study suggested an association between SORCS1 variants and guide dog training outcomes. However, this result relied on only 28 dogs and lacked sufficient statistical power. In this study, we expanded the sample size and evaluated the association between SORCS1 polymorphisms and behavioral suitability in 160 dogs, using pass/fail training outcomes as behavioral trait indicators. We initially validated 12 candidate SNPs within SORCS1 using Sanger sequencing in 64 dogs, revealing significant genotype-dependent differences for eight loci located in predicted intron 3. A tagging SNP (rs23402730, C > T) was subsequently genotyped in 160 dogs (65 successful and 95 unsuccessful). The strongest association was detected under a recessive model (CC + CT vs. TT), yielding P = 4.7 × 10 ⁻ ⁵ and an odds ratio (OR) of 4.11 (95% CI: 2.07-8.18). As allele frequencies and genetic relatedness varied among dogs, we further evaluated the association using generalized linear mixed-effects models adjusting for sex, breed, and family structure. In the full dataset (n = 159), the additive genotype remained statistically significant (β = 2.20, P = 4.5 × 10 ⁻ 4; OR = 8.98, 95% CI: 2.64-30.59). Moreover, we confirmed the association in a genetically homogeneous subset of 114 Labrador retrievers, independent of breed effects (P = 0.029; OR = 4.71, 95% CI: 1.17-18.99). These results suggest that variation in SORCS1 is associated with behavioral suitability in dogs, based on an expanded cohort with guide dog training outcomes. As behavior is polygenic, SORCS1 represents one contributing locus that may be informative for future genetic studies aimed at elucidating the molecular basis of canine behavior.

Indexed as

Behavior, AnimalAnimalsDogsFemaleGenome-Wide Association StudyGenotypeMalePolymorphism, Single Nucleotide

Identifiers

PMID41701742
PMCPMC12912605

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.