Evidence map›Paper›PMID 41021661›Full record

ArticlePLoS genetics2025

Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screen.

Janine M Wotton, Mark P Krebs, Riccardo Sangermano, Jessica K Wong, Cynthia Smith, Amelia M Willett, Douglas Howell, Abby Jones, Catherine Witmeyer, Jacob P Lowy and 9 more

Abstract read
In one paragraph

Article in PLoS genetics, 2025. 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

19 authors.

Janine M WottonCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.ORCID https://orcid.org/0000-0002-1899-9452
Mark P KrebsMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.ORCID https://orcid.org/0000-0001-9017-6066
Riccardo SangermanoOcular Genomics Institute, Massachusetts Eye and Ear, Boston, Massachusetts, United States of America.
Jessica K WongPathology Services, The Jackson Laboratory, Sacramento, California, United States of America.ORCID https://orcid.org/0000-0003-1709-3357
Cynthia SmithMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Amelia M WillettCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Douglas HowellCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Abby JonesCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Catherine WitmeyerCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Jacob P LowyCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.ORCID https://orcid.org/0000-0001-8504-7518
Michael McFarlandMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Stephan A MurrayMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Robert E BraunMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Patsy M NishinaMammalian Genetics, The Jackson Laboratory, Bar Harbor, Maine, United States of America.
Eric A PierceOcular Genomics Institute, Massachusetts Eye and Ear, Boston, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-2354-4102
Emily M PlaceOcular Genomics Institute, Massachusetts Eye and Ear, Boston, Massachusetts, United States of America.
Kinga M BujakowskaOcular Genomics Institute, Massachusetts Eye and Ear, Boston, Massachusetts, United States of America.
Neal S PeacheyOphthalmic Research, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
Jacqueline K WhiteCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, Maine, United States of America.ORCID https://orcid.org/0000-0001-6268-2826

Funding

The Jackson Laboratory Knockout Mouse Production and Phenotyping Project (JAX KOMP2)UM1OD023222 · OD · JACKSON LABORATORY · PI ROBERT E BRAUN, Stephen A Murray · 2016 to 2026
$47.2M
Precision Medicine for Inherited Retinal DegenerationsR01EY012910 · NEI · UNIVERSITY OF PENNSYLVANIA · PI Eric A Pierce · 1999 to 2026
$15.9M
P30 Core Grant for Vision ResearchP30EY014104 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Janey L Wiggs · 2002 to 2026
$15.1M
RESOURCE/SERVICE CORE C - MOLECULAR INFORMATICS MODULEP30EY025585 · NEI · CLEVELAND CLINIC LERNER COM-CWRU · PI BELA ANAND-APTE · 2016 to 2026
$7.7M
Genetic Modifiers of Retinal DiseaseR01EY027305 · NEI · JACKSON LABORATORY · PI Patsy M Nishina · 2017 to 2026
$5.2M
Finding Missing Genetic Causality of Inherited Retinal DegenerationsR01EY035717 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Kinga Bujakowska · 2024 to 2026
$2.1M
BLRD VA IK6 BX005233NEI NIH HHS P30 EY014104NEI NIH HHS P30 EY025585NEI NIH HHS R01 EY012910NEI NIH HHS R01 EY027305NEI NIH HHS R01 EY035717NIH HHS UM1 OD023222
6 · The paper itself

Abstract

Electroretinography (ERG) provides a noninvasive functional measure of multiple cell types of the outer retina. We conducted an ERG-based screen of 530 single-gene knockout mouse strains generated as part of the International Mouse Phenotyping Consortium, representing 2.5% of all protein-coding genes, to identify genetic variants affecting retinal function. We identified 30 strains with significantly altered ERG amplitudes. Two of the genes identified, Cfap418 and Syne2, have been previously reported with outer retinal dysfunction, thereby serving as internal controls that validate our screening protocol. Of the remaining 28 genes newly associated with altered retinal function, the majority lacked a contemporaneous histopathology correlate, highlighting the importance of ERG in early detection of functional abnormalities. A rare homozygous missense variant in FCHSD2, the human orthologue of one of the 28 genes identified, was found in a patient presenting with retinal degeneration that lacked a molecular diagnosis. This report represents a useful resource for future investigations into the molecular mechanisms driving inherited retinal diseases and demonstrates the power of large-scale ERG screening in identifying novel genetic determinants of retinal function.

Indexed as

RetinaRetinal DegenerationAnimalsElectroretinographyHumansMiceMice, KnockoutNerve Tissue ProteinsNerve Tissue Proteins

Identifiers

PMID41021661
PMCPMC12503315

What OpenQuestion holds

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Registered trials

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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.