Evidence map›Paper›PMID 40131457›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2025

The RSPO2 gene is associated with bilateral anterior amelia in Chihuahuas.

Lucie Chevallier, Marin Green, Julia Vo, Karen Vernau, Denis J Marcellin-Little, Vidhya Jagannathan, Tosso Leeb, Danika Bannasch

Abstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Lucie Chevallier *INSERM, UPEC, Ecole Nationale Vétérinaire d'Alfort, U955 - IMRB, Team 10 - Biology of the Neuromuscular System, Maisons-Alfort, France.ORCID 0000-0001-8602-1993
Marin Green *Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.
Julia VoDepartment of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.ORCID 0009-0002-6951-9524
Karen VernauDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.ORCID 0000-0002-8062-0028
Denis J Marcellin-LittleDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.ORCID 0000-0001-6596-5928
Vidhya JagannathanInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.ORCID 0000-0002-8155-0041
Tosso LeebInstitute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.ORCID 0000-0003-0553-4880
Danika BannaschDepartment of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA. dlbannasch@ucdavis.edu.ORCID 0000-0002-7614-7207

Funding

Students Training in Advanced Research (STAR) ProgramT35OD010956 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DANIKA L BANNASCH · 2012 to 2026
$1.6M
NIH HHS T35 OD010956NIH HHS T35-OD010956
6 · The paper itself

Abstract

Bilateral anterior amelia (BAA) is the congenital absence of thoracic limbs and has been reported in the Chihuahua as an autosomal recessive disorder. In some cases, the digits of the pelvic limbs can be variably affected, but otherwise, the pelvic limbs are generally spared. A GWAS performed with nine BAA affected Chihuahuas identified a significant association on chromosome 13, and homozygosity mapping delineated a 2.1 Mb chromosomal region containing the RSPO2 gene. Loss of function variants of RSPO2 in humans and cattle has been associated with the absence of all limbs. Six affected Chihuahuas were whole genome sequenced (WGS) and aligned to the CanFam4 assembly. SNVs, small indels, and structural variants within the critical interval that fitted a recessive model were investigated. Three SNVs (NC_049234.1:g.8891861C > T; NC_049234.1:g.8974204C > T and NC_049234.1:g.9789424G > A) were homozygous in five cases and absent from 3,418 genetically diverse control genome sequences, except for one Small Poodle that was heterozygous. One SNV resided in RSPO2's second intron, while the two others were intergenic. The three candidate variants were genotyped in 7 additional cases and 100 control Chihuahuas. Twelve of 13 cases were homozygous for the mutant allele, and one case was heterozygous. Controls were either homozygous for the reference allele (97%) or heterozygous (3%). Our data should facilitate genetic testing of Chihuahuas to prevent the unintentional production of BAA affected dogs. Moreover, the identification of these variants enhances understanding of RSPO2 gene function in limb development.

Indexed as

Dog DiseasesEctromeliaThrombospondinsAnimalsDogsFemaleGenome-Wide Association StudyHomozygoteHumansMalePolymorphism, Single NucleotideThrombospondins

Identifiers

PMID40131457
PMCPMC12408703

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.