Evidence map›Paper›PMID 42087835›Full record

ArticleAnimal genetics2026

Straightened Small Pinnae in TRPV4 c.1024G>T Heterozygous Cats.

Yuki Matsumoto, Ryuga Ishii, Hisashi Ukawa, Saaya Hiyoshi-Kanemoto, Hinako Hayashi, Haruka Onishi, Kai Ataka, Ryo Horie

Abstract read
In one paragraph

Article in Animal genetics, 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yuki MatsumotoGenetic Testing Section, Anicom Pafe Inc, Yokohamashi-Nakaku, Kanagawa, Japan.ORCID https://orcid.org/0000-0002-9143-3498
Ryuga IshiiResearch and Development Section, Anicom Specialty Medical Institute Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Hisashi UkawaGenetic Testing Section, Anicom Pafe Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Saaya Hiyoshi-KanemotoResearch and Development Section, Anicom Specialty Medical Institute Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Hinako HayashiGenetic Testing Section, Anicom Pafe Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Haruka OnishiGenetic Testing Section, Anicom Pafe Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Kai AtakaGenetic Testing Section, Anicom Pafe Inc, Yokohamashi-Nakaku, Kanagawa, Japan.
Ryo HorieResearch and Development Section, Anicom Specialty Medical Institute Inc, Yokohamashi-Nakaku, Kanagawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The folded-ear phenotype of Scottish Fold cats results from a dominant variant of the TRPV4 gene (c.1024G>T). Producing homozygous individuals is discouraged due to severe osteochondrodysplasia and identifying heterozygous carriers is critical for breeding. Although carriers are generally expected to have folded ears, straight-eared individuals have also been suspected among them. Here, we investigated the relationship between ear phenotype and TRPV4 genotype using longitudinal photographic data and TRPV4 genotyping in 114 cats. We identified seven individuals that transitioned from folded to straight ear phenotype during maturation. Genotyping confirmed all were heterozygous carriers, with 12.7% found among heterozygous cats. Morphometric analysis of 14 cats with high-quality photographs demonstrated these "straightened" cats had smaller pinnae than genetically wild-type straight-eared cats (p < 0.05), suggesting cartilage anomalies. These findings confirm "cryptic folds"-phenotypically straight but genetically heterozygous cats. Consequently, visual inspection for breeding selection is insufficient, highlighting the necessity of TRPV4 genotyping to prevent unintentional production of homozygous offspring with severe osteochondrodysplasia.

Indexed as

TRPV Cation ChannelsAnimalsBreedingCatsFemaleGenotypeHeterozygoteMalePhenotypeTRPV Cation Channelsdomestic catfold earScottish foldsTRPV4

Identifiers

PMID42087835
PMCPMC13147223

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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.