Accession PRJCA012140
Title Genetic analysis of variants of the MYH6 gene promoter in tetralogy of fallot
Relevance Medical
Data types Genome sequencing
Organisms Homo sapiens
Description Tetralogy of fallot (TOF) is one of the common congenital heart diseases. The MYH6 gene has a critical role in cardiac development but the role of MYH6 promoter variants in patients with ASD has not been explored. In 315 TOF patients, we investigated the MYH6 gene promoter variants and verified the effect on gene expression by using cellular functional experiments and bioinformatics analysis.
Sample scope Multiisolate
Release date 2022-09-26
Publication
PubMed ID Article title Journal name DOI Year
38135727 Tetralogy of Fallot: variants of MYH6 gene promoter and cellular functional analyses Pediatric Research 10.1038/s41390-023-02955-x 2023
Grants
Agency program Grant ID Grant title
National Natural Science Foundation of China (NSFC) 82170353
National Natural Science Foundation of China (NSFC) 81870288
TEDA International Cardiovascular Hospital 2021-TD-006
Submitter JiyYang Zuo (jiyangzuo@163.com)
Organization Tianjin Medical University
Submission date 2022-09-26

Project Data

Resource name Description