Evidence map›Paper›PMID 34945726›Full record

ArticleJournal of personalized medicine2021

Identification of a Rare Novel KMT2C Mutation That Presents with Schizophrenia in a Multiplex Family.

Chia-Hsiang Chen, Ailing Huang, Yu-Shu Huang, Ting-Hsuan Fang

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Biomolecules · 2025
    Article
  2. Article
  3. Novel germline variants inFrontiers in neurology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. KMT2C knockout generates ASD-like behaviors in mice.Frontiers in cell and developmental biology · 2023
    Article
  8. 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

4 authors at 3 institutions in 1 country.

Chia-Hsiang ChenDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.ORCID 0000-0002-8232-2403
Ailing HuangDepartment of Psychiatry, Yuli Branch, Taipei Veterans General Hospital, Hualien 981, Taiwan.
Yu-Shu HuangDepartment of Psychiatry, Chang Gung Memorial Hospital-Linkou, Taoyuan 333, Taiwan.ORCID 0000-0002-4015-5942
Ting-Hsuan FangDepartment and Institute of Biomedical Sciences, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
Chang Gung University · TWChang Gung Memorial Hospital · TWTaipei Veterans General Hospital · TW

Funding

Linkou Chang Gung Memorial Hospital CMRP3G1911, CORPG3J0311, CORPG3J0312, CORPG3J0313Ministry of Science and Technology, Taiwan 107-2314-B-182-057-MY2
6 · The paper itself

Abstract

Schizophrenia is a complex genetic disorder involving many common variants with modest effects and rare mutations with high penetrance. Rare mutations associated with schizophrenia are highly heterogeneous and private for affected individuals and families. Identifying such mutations can help establish the molecular diagnosis, elucidate the pathogenesis, and provide helpful genetic counseling for affected patients and families. We performed a whole-exome sequencing analysis to search for rare pathogenic mutations co-segregating with schizophrenia transmitted in a dominant inheritance in a two-generation multiplex family. We identified a rare missense mutation H1574R (Histidine1574Arginine, rs199796552) of KMT2C (lysine methyltransferase 2C) co-segregating with affected members in this family. The mutation is a novel deleterious mutation of KMT2C, not reported before in the literature. The KMT2C encodes a histone 3 lysine 4 (H3K4)-specific methyltransferase and involves epigenetic regulation of brain gene expression. Mutations of KMT2C have been found in neurodevelopmental disorders, such as Kleefstra syndrome, intellectual disability, and autism spectrum disorders. Our finding suggests that schizophrenia might be one of the clinical phenotype spectra of KMT2C mutations, and KMT2C might be a novel risk gene for schizophrenia. Nevertheless, the co-segregation of this mutation with schizophrenia in this family might also be due to chance; functional assays of this mutation are needed to address this issue.

Indexed as

histone 3 lysine 4KMT2Cmethylationrare mutationschizophreniawhole-genome sequencing

Identifiers

PMID34945726
PMCPMC8707139
OpenAlexW3216878880

What OpenQuestion holds

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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.