Evidence map›Paper›PMID 30886859›Full record

ArticleBioMed research international2019

A Genetic Variant in GPR126 Causing a Decreased Inclusion of Exon 6 Is Associated with Cartilage Development in Adolescent Idiopathic Scoliosis Population.

Enjie Xu, Wei Shao, Heng Jiang, Tao Lin, Rui Gao, Xuhui Zhou

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. The far extracellular CUB domain of the adhesion GPCR ADGRG6/GPR126 is a key regulator of receptor signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. Progesterone activates GPR126 to promote breast cancer development via the Gi pathway.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

6 authors at 1 institution in 1 country.

Enjie XuDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Wei ShaoDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Heng JiangDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Tao LinDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Rui GaoDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.ORCID 0000-0003-0695-7180
Xuhui ZhouDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai, China.ORCID 0000-0002-8026-5468
Second Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adolescent idiopathic scoliosis (AIS) is the most common spinal deformity disease in adolescents but its etiology and pathogenesis are still unclear. The current study aims to identify the relationship between single nucleotide polymorphisms (SNPs) of G protein-coupled receptor 126 (GPR126) gene and AIS predisposition. GPR126 contains 26 exons and alternative splicing of exon 6 and exon 25 produces 4 protein-coding transcripts. We genotyped SNPs of GPR126 gene around exon 6 and exon 25 in 131 Chinese AIS patients and 132 healthy controls and provided evidence that SNP rs41289839 G>A is strongly associated with AIS susceptibility. Linkage disequilibrium analysis suggests that rs41289839 and other AIS-related SNPs were in strong LD. Next, we demonstrated that rs41289839 G>A inhibits the inclusion of exon 6 during alternative splicing, resulting in a decreased expression level of exon 6-included transcript (GPR126-exon6

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdolescentAdultAgedAllelesCartilageCell DifferentiationChildChondrogenesisExonsFemaleGenotypeHumansLinkage DisequilibriumMaleADGRG6 protein, humanReceptors, G-Protein-Coupled

Identifiers

PMID30886859
PMCPMC6388357
OpenAlexW2913333282

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.