Evidence map›Paper›PMID 28455698›Full record

ArticleMolecular neurobiology2018

TMEM230 Mutations Are Rare in Han Chinese Patients with Autosomal Dominant Parkinson's Disease.

Qianqian Wei, Ruwei Ou, Qingqing Zhou, Yongping Chen, Bei Cao, Xiaojing Gu, Bi Zhao, Ying Wu, Wei Song, Hui-Fang Shang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Glycosylation Regulation by TMEM230 in Aging and Autoimmunity.International journal of molecular sciences · 2025
    Article
  2. Review
  3. Article
  4. The Role of TMEM230 Gene in Parkinson's Disease.Journal of Parkinson's disease · 2018
    Review
  5. 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 at 2 institutions in 1 country.

Qianqian WeiDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Ruwei OuDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Qingqing ZhouDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Yongping ChenDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Bei CaoDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Xiaojing GuDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Bi ZhaoDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Ying WuDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Wei SongDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.
Hui-Fang ShangDepartment of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China. hfshang2002@163.com.
Sichuan University · CNWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the gene encoding the transmembrane protein 230 (TMEM230) have been reported in patients with familial, autosomal dominant inherited Parkinson's disease (ADPD). The aim of the present study was to explore the role and the prevalence of TMEM230 mutations in Chinese patients with ADPD. A cohort of 120 patients with ADPD and 650 healthy controls (HCs) from the Department of Neurology, West China Hospital of Sichuan University was screened. The entire coding exons of TREM230 in all the patients, as well as exon 5 of this gene in the 650 HCs, were directly sequenced with the Sanger sequencing approach. Novel identified mutations or variants of Parkinson's disease were tested in all HCs in the corresponding chromosomal regions. Two novel variants of the TMEM230 gene were identified. The c.46G>T [p. Gly16Trp] variant in exon 1 was identified in a male PD patient, while a heterozygous frameshift variant, c.429delT [p. Val143ValfsX4], in exon 5 was found in an HC. However, the most commonly reported mutation, p.*184ProGlyext*5, was not detected in either the patients or control subjects in this study. Our findings suggested that TMEM230 mutations are very rare in the ADPD Han Chinese population. Further evaluation of genetic data from a larger sample population is required to understand the genetic role of TMEM230 in the etiology of PD.

Indexed as

Amino Acid SequenceAsian PeopleBase SequenceEthnicityFemaleHumansMaleMembrane ProteinsMiddle AgedMutationParkinson DiseaseMembrane ProteinsTMEM230 protein, humanAutosomal dominant inheritanceMutationParkinson’s diseaseTMEM230

Identifiers

PMID28455698
OpenAlexW2609595681

What OpenQuestion holds

Textmetadata
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.