Evidence map›Paper›PMID 41805112›Full record

ArticleJournal of cell science2026

The EH-binding protein EHBP1 operates in a ciliary functional module affected by INPP5E dysfunction.

Kae R Whiting, Mariam Aslanyan, Imke Peters, Stef Letteboer, Ideke J C Lamers, Mohamed-Ali Jarboui, Tina Beyer, Katrin Dahlke, Karsten Boldt, Ronald Roepman

Abstract read
In one paragraph

Article in Journal of cell science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Kae R WhitingDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.ORCID 0000-0002-2100-6597
Mariam AslanyanDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.ORCID 0000-0001-5675-2031
Imke PetersDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.
Stef LetteboerDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.ORCID 0000-0003-2089-5000
Ideke J C LamersDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.
Mohamed-Ali JarbouiEberhard Karls University of Tübingen, Core Facility for Medical Proteomics, 72074 Tübingen, Germany.ORCID 0000-0002-5203-235X
Tina BeyerEberhard Karls University of Tübingen, Institute for Ophthalmic Research, 72074 Tübingen, Germany.ORCID 0000-0002-6302-8997
Katrin DahlkeEberhard Karls University of Tübingen, Core Facility for Medical Proteomics, 72074 Tübingen, Germany.ORCID 0000-0001-9681-2908
Karsten BoldtEberhard Karls University of Tübingen, Core Facility for Medical Proteomics, 72074 Tübingen, Germany.ORCID 0000-0002-2693-689X
Ronald RoepmanDepartment of Human Genetics, Research Institute for Medical Innovation, Radboud University Medical Center, 6525 GA, Nijmegen, Netherlands.ORCID 0000-0002-5178-8163

Funding

Dutch ministry of Education, Culture and Sciences 02.006.034H2020 Marie Sklodowska-Curie Actions 861329H2020 Marie Skłodowska-Curie Actions 861329Landelijke Stichting voor Blinden en SlechtziendenMinisterie van Onderwijs, Cultuur en Wetenschap gravitation grant 024.006.034 Lifelong VISIONOogfonds Uitzicht 2023-32Radboud UniversityStichting BlindenhulpStichting tot Verbetering van het Lot der BlindenStichting Usher SyndroomStichting voor gehandicapte kinderen DowilvoTistou and Charlotte Kerstan StiftungUitzicht 2023-32
6 · The paper itself

Abstract

Inositol polyphosphate-5-phosphatase E (INPP5E) encodes the ciliary protein INPP5E, which plays an important role in regulating the phospholipid membrane makeup of the primary cilium. Here, we utilize proximity labeled proteomics of INPP5E to broaden the number of known functional modules that work in close proximity to the protein. In doing so, we identified the EH-binding protein EHBP1 as a ciliary protein that localizes to the basal body and ciliary compartment of the primary cilium in human-derived fibroblasts and RPE cells. Additionally, we show that EHBP1 localizes to the rudimentary outer segment membrane of developing photoreceptors in retinal organoids. Dysfunction of INPP5E - either due to pathogenic variants in human fibroblasts or CRISPR/Cas9-generated loss-of-function variants in human retinal organoids - causes the localization of EHBP1 to be altered. Our data suggest that EHBP1 functions at the primary cilium and photoreceptors, where it is regulated by INPP5E. This provides further insights into the disease pathogenesis of retinal ciliopathies caused by pathogenic variants in INPP5E, and suggests that EHBP1 might be a candidate gene for retinal ciliopathies.

Indexed as

Carrier ProteinsCiliaPhosphoric Monoester HydrolasesAnimalsFibroblastsHumansPhosphoinositide 5-PhosphatasesCarrier ProteinsPhosphoinositide 5-PhosphatasesPhosphoric Monoester HydrolasesBioIDEHBP1INPP5EPrimary ciliumProximity proteomics

Identifiers

PMID41805112
PMCPMC13450894

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.