Evidence map›Paper›PMID 33767456›Full record

ArticleEuropean journal of human genetics : EJHG2021

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.

Nikolay A Barashkov, Fedor A Konovalov, Tuyara V Borisova, Fedor M Teryutin, Aisen V Solovyev, Vera G Pshennikova, Nadejda V Sapojnikova, Lyubov S Vychuzhina, Georgii P Romanov, Nyurgun N Gotovtsev and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Exploiting autophagy and related pathways: pioneering new horizons in cataract therapy.Apoptosis : an international journal on programmed cell death · 2025
    Review
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  8. Genes · 2022
    Article
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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

17 authors at 4 institutions in 2 countries.

Nikolay A BarashkovLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation. barashkov2004@mail.ru.ORCID http://orcid.org/0000-0002-6984-7934
Fedor A KonovalovGenomed Ltd, Moscow, Russian Federation.
Tuyara V BorisovaLaboratory of Molecular Biology, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation.
Fedor M TeryutinLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.
Aisen V SolovyevLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.
Vera G PshennikovaLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.
Nadejda V SapojnikovaDepartment of Ophthalmology, Republican Hospital #1 - National Centre of Medicine, Yakutsk, Russian Federation.
Lyubov S VychuzhinaDepartment of Ophthalmology, Republican Hospital #1 - National Centre of Medicine, Yakutsk, Russian Federation.
Georgii P RomanovLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.ORCID http://orcid.org/0000-0002-2936-5818
Nyurgun N GotovtsevLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.
Igor V MorozovSB RAS Genomics Core Facility, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation.ORCID http://orcid.org/0000-0002-0307-4203
Alexander A BondarSB RAS Genomics Core Facility, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation.ORCID http://orcid.org/0000-0001-9181-0487
Fedor A PlatonovMedical Institute, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation.
Tatiana E BurtsevaMedical Institute, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation.
Elza K KhusnutdinovaLaboratory of Molecular Biology, M.K. Ammosov North-Eastern Federal University, Yakutsk, Russian Federation.ORCID http://orcid.org/0000-0003-2987-3334
Olga L PosukhNovosibirsk State University, Novosibirsk, Russian Federation.
Sardana A FedorovaLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yakutsk, Russian Federation.
North-Eastern Federal University · RUNational Hospital · INNovosibirsk State University · RUInstitute of Chemical Biology and Fundamental Medicine · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital autosomal recessive cataract with unknown genetic etiology is one of the most common Mendelian diseases among the Turkic-speaking Yakut population (Eastern Siberia, Russia). To identify the genetic cause of congenital cataract spread in this population, we performed whole-exome sequencing (Illumina NextSeq 500) in one Yakut family with three affected siblings whose parents had preserved vision. We have revealed the novel homozygous c.1621C>T transition leading to premature stop codon p.(Gln541*) in exon 8 of the FYCO1 gene (NM_024513.4). Subsequent screening of c.1621C>T p.(Gln541*) revealed this variant in a homozygous state in 25 out of 29 Yakut families with congenital cataract (86%). Among 424 healthy individuals from seven populations of Eastern Siberia (Russians, Yakuts, Evenks, Evens, Dolgans, Chukchi, and Yukaghirs), the highest carrier frequency of c.1621C>T p.(Gln541*) was found in the Yakut population (7.9%). DNA samples of 25 homozygous for c.1621C>T p.(Gln541*) patients with congenital cataract and 114 unaffected unrelated individuals without this variant were used for a haplotype analysis based on the genotyping of six STR markers (D3S3512, D3S3685, D3S3582, D3S3561, D3S1289, and D3S3698). The structure of the identified haplotypes indicates a common origin for all of the studied mutant chromosomes bearing c.1621C>T p.(Gln541*). The age of the с.1621C>T p.(Gln541*) founder haplotype was estimated to be approximately 260 ± 65 years (10 generations). These findings characterize Eastern Siberia as the region of the world with the most extensive accumulation of the unique variant c.1621C>T p.(Gln541*) in the FYCO1 gene as a result of the founder effect.

Indexed as

Founder EffectCataractChildCodon, TerminatorGene FrequencyGenes, RecessiveHomozygoteHumansIndigenous PeoplesMicrotubule-Associated ProteinsMutationSiberiaCodon, TerminatorFYCO1 protein, humanMicrotubule-Associated Proteins

Identifiers

PMID33767456
PMCPMC8187664
OpenAlexW3136689014

What OpenQuestion holds

Textmetadata
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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.