Evidence map›Paper›PMID 31746431›Full record

Trial reportMolecular medicine reports2020

A novel GPR143 mutation in a Chinese family with X‑linked ocular albinism type 1.

Xuhui Gao, Tiecheng Liu, Xuan Cheng, Aiai Dai, Wei Liu, Runpu Li, Maonian Zhang

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Genes · 2025
    Review
  2. Review
  3. Article
  4. Molecular vision · 2023
    Article
  5. Article
  6. 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

7 authors at 1 institution in 1 country.

Xuhui GaoDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Tiecheng LiuDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Xuan ChengDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Aiai DaiDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Wei LiuDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Runpu LiDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Maonian ZhangDepartment of Ophthalmology, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ocular albinism type 1 (OA1) is a genetic disorder characterized by reduced eye pigmentation and nystagmus, which is often accompanied by decreased visual acuity, strabismus and other symptoms, whereas skin and hair color remain normal. The present study aimed to assess the clinical features and perform genotype analysis of a family with OA1, and to determine the disease‑causing mutation. A total of 18 family members (nine affected patients and nine normal subjects) from Hainan, China, were recruited to the present study in December 2017. A detailed clinical ophthalmic examination was performed for all participants, including a visual acuity test, anterior segment slit lamp examination, eye fundus examination and optical coherence tomography. Mutations in the G protein‑coupled receptor 143 (GPR143) gene were determined by DNA sequencing assays and polymerase chain reaction assays for deletions; all exon coding sequences, exons at the 5'‑ and 3'‑ends, and non‑coding region sequences of intron splicing were assessed. Within the family, nine male patients exhibited disease occurrence at the age of 0‑6 months. All patients presented with different degrees of iris depigmentation, horizontal jerk nystagmus, foveal hypoplasia and reduced visual acuity. The fundus of only one patient exhibited choroid coloboma; in the remaining patients, their fundi exhibited different degrees of irregular retinal depigmentation. The mutation c.360+5G>T in the GPR143 gene was identified in this family. In conclusion, the present study identified the splicing mutation c.360+5G>T in the GPR143 gene in a Chinese family with OA1 and successfully identified the site. To the best of our knowledge, there have been no previous reports regarding this mutation in any major genome databases; therefore, this outcome may enrich the mutation spectrum of the GPR143 gene.

Indexed as

Asian PeopleFamilyMutationAdolescentAdultAgedAlbinism, OcularChinaEye ProteinsFemaleHumansMaleMembrane GlycoproteinsMiddle AgedEye ProteinsGPR143 protein, humanMembrane GlycoproteinsG protein-coupled receptor 143 genemutationocular albinism type 1X-linked recessive inheritance

Identifiers

PMID31746431
PMCPMC6896309
OpenAlexW2986824595

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.