Evidence map›Paper›PMID 36047852›Full record

ArticleG3 (Bethesda, Md.)2022

An SNN retrocopy insertion upstream of GPR22 is associated with dark red coat color in Poodles.

Kevin Batcher, Scarlett Varney, Verena K Affolter, Steven G Friedenberg, Danika Bannasch

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 36% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Absence ofVeterinary sciences · 2025
    Article
  2. Article
  3. 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

5 authors at 2 institutions in 1 country.

Kevin BatcherDepartment of Population Health and Reproduction, University of California, Davis, Davis, CA 95616, USA.ORCID 0000-0002-1048-1130
Scarlett VarneyDepartment of Population Health and Reproduction, University of California, Davis, Davis, CA 95616, USA.ORCID 0000-0001-9028-1114
Verena K AffolterDepartment of Pathology, Microbiology, & Immunology, University of California, Davis, Davis, CA 95616, USA.ORCID 0000-0003-1118-9016
Steven G FriedenbergDepartment of Veterinary Clinical Sciences, University of Minnesota, St Paul, MN 55455, USA.ORCID 0000-0002-7510-2322
Danika BannaschDepartment of Population Health and Reproduction, University of California, Davis, Davis, CA 95616, USA.ORCID 0000-0002-7614-7207
University of California, Davis · USUniversity of Minnesota · US

Funding

Immunological Basis of Autoimmune Addison's Disease in a Novel Canine Model SystemK01OD027058 · OD · UNIVERSITY OF MINNESOTA · PI FRIEDENBERG, STEVEN GENE · 2019 to 2023
$724k
NIH HHS K01 OD027058
6 · The paper itself

Abstract

Pigment production and distribution is controlled through multiple genes, resulting in a wide range of coat color phenotypes in dogs. Dogs that produce only the pheomelanin pigment vary in intensity from white to deep red. The Poodle breed has a wide range of officially recognized coat colors, including the pheomelanin-based white, cream, apricot, and red coat colors, which are not fully explained by the previously identified genetic variants involved in pigment intensity. Here, a genome-wide association study for pheomelanin intensity was performed in Poodles which identified an association on canine chromosome 18. Whole-genome sequencing data revealed an SNN retrocopy insertion (SNNL1) in apricot and red Poodles within the associated region on chromosome 18. While equal numbers of melanocytes were observed in all Poodle skin hair bulbs, higher melanin content was observed in the darker Poodles. Several genes involved in melanogenesis were also identified as highly overexpressed in red Poodle skin. The most differentially expressed gene however was GPR22, which was highly expressed in red Poodle skin while unexpressed in white Poodle skin (log2 fold change in expression 6.1, P < 0.001). GPR22 is an orphan G-protein-coupled receptor normally expressed exclusively in the brain and heart. The SNNL1 retrocopy inserted 2.8 kb upstream of GPR22 and is likely disrupting regulation of the gene, resulting in atypical expression in the skin. Thus, we identify the SNNL1 insertion as a candidate variant for the CFA18 pheomelanin intensity locus in red Poodles.

Indexed as

Genome-Wide Association StudyPigmentationAnimalsDogsPhenotypeWhole Genome Sequencingcaninecoat colordogGWASinheritedpheomelaninretrogene

Identifiers

PMID36047852
PMCPMC9635648
OpenAlexW4294011881

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.