Evidence map›Paper›PMID 42575711›Full record

ArticleAnimal genetics2026

SOAT1 Nonsense Variant in a Cat With Sebaceous Gland Dysplasia.

Lia Kammermann, Joanne K Mansell, Barbara G McMahill, Verena K Affolter, Vidhya Jagannathan, Tosso Leeb

Abstract readCase Reports
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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

6 authors.

Lia KammermannInstitute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0009-0003-5658-6493
Joanne K MansellDermatopathology Specialty Service, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas, USA.ORCID https://orcid.org/0000-0001-6426-9867
Barbara G McMahillPathology Services, IDEXX Reference Laboratories Inc., Lander, Wyoming, USA.ORCID https://orcid.org/0000-0003-2010-8038
Verena K AffolterDepartment of Pathology, Microbiology, Immunology, School of Veterinary Medicine, University California Davis, Davis, California, USA.ORCID https://orcid.org/0000-0003-1118-9016
Vidhya JagannathanInstitute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0002-8155-0041
Tosso LeebInstitute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland.ORCID https://orcid.org/0000-0003-0553-4880

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated a random-bred cat with sebaceous gland dysplasia. The cat presented with hypotrichosis and dark crusts on the skin. Histopathologically, sebaceous glands were enlarged and had an abnormal morphology with an increased number of undifferentiated reserve cells. Whole genome sequence analysis of the affected cat and comparison to 106 genomes of genetically diverse cats revealed a private homozygous nonsense variant in the functional candidate gene SOAT1 encoding sterol O-acyltransferase 1, XM_011291017.4:c.1221G>A or XP_011289319.1:p.(Trp407*). Based on the known role of SOAT1 in sebaceous gland function, the identified variant most likely represents the cause for the phenotype. To the best of our knowledge, we report the second pathogenic SOAT1 variant in cats. These results enable diagnostic genetic testing should any new cases come under veterinary care, detection of unaffected carrier animals, and strengthen the gene-phenotype relationship between SOAT1 and sebaceous gland dysplasias.

Indexed as

Cat DiseasesCodon, NonsenseSebaceous Gland DiseasesSebaceous GlandsSterol O-AcyltransferaseAnimalsCatsFemalePhenotypeCodon, NonsenseSterol O-Acyltransferasesterol O-acyltransferase 1animal modeldermatologyFelis catusprecision medicineveterinary medicine

Identifiers

PMID42575711
PMCPMC13456967

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Registered trials

None linked

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.