
==== Front
Heliyon
Heliyon
Heliyon
2405-8440
Elsevier

S2405-8440(24)13208-2
10.1016/j.heliyon.2024.e37177
e37177
Research Article
Discovery of a novel mutation F184S (c.551T>C) in GATA4 gene causing congenital heart disease in a consanguineous Saudi family
Rasool Mahmood mahmoodrasool@yahoo.com
mrahmed1@kau.edu.sa
a⁎
Pushparaj Peter Natesan a
Haque Absarul b
Shorbaji Ayat Mohammed ac
Mira Loubna Siraj a
Bakhashab Sherin ac
Alama Mohamed Nabil d
Farooq Muhammad e
Karim Sajjad a
Larsen Lars Allan f
a Center of Excellence in Genomic Medicine Research, Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
b King Fahd Medical Research Center, Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
c Department of Biochemistry, King Abdulaziz University, Jeddah, Saudi Arabia
d Department of Cardiology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia
e Department of Bioinformatics and Biotechnology, Government College University, Faisalabad, Pakistan
f Department of Cellular and Molecular Medicine, University of Copenhagen, Denmark
⁎ Corresponding author. mahmoodrasool@yahoo.commrahmed1@kau.edu.sa
29 8 2024
15 9 2024
29 8 2024
10 17 e3717727 11 2023
25 8 2024
28 8 2024
© 2024 The Authors
2024
https://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Background & aim

Congenital heart disease (CHD) is the most common cause of non-infectious deaths in infants worldwide. However, the molecular mechanisms underlying CHD remain unclear. Approximately 30 % of the causes are believed to be genetic mutations and chromosomal abnormalities. In this study, we aimed to identify the genetic causes of CHD in consanguineous families.

Methods

Fourth-generation pedigrees with CHD were recruited. The main cardiac features of the patient included absence of the right pulmonary artery and a large dilated left pulmonary artery. To determine the underlying genetic cause, whole-exome sequencing was performed and subsequently confirmed using Sanger sequencing and different online databases to study the pathogenesis of the identified gene mutation. An in-silico homology model was created using the Alphafold homology model structure of GATA4 (AF-P43694-F1). The missense3D online program was used to evaluate the structural alterations.

Results

We identified a deleterious mutation c.551T > C (p.Phe184Ser) in GATA4. GATA4 is a highly conserved zinc-finger transcription factor, and its continuous expression is essential for cardiogenesis during embryogenesis. The in-silico model suggested a compromised binding efficiency with other proteins. Several variant interpretation algorithms indicated that the F184S missense variant in GATA4 is damaging, whereas HOPE analysis indicated the functional impairment of DNA binding of transcription factors and zinc-ion binding activities of GATA4.

Conclusion

The variant identified in GATA4 appears to cause recessive CHD in the family. In silico analysis suggested that this variant was damaging and caused multiple structural and functional aberrations. This study may support prenatal screening of the fetus in this family to prevent diseases in new generations.

Keywords

GATA4
F184S
Congenital heart disease
Whole exome sequencing
Homology modelling
==== Body
pmc1 Introduction

Congenital heart disease (CHD) is the most common birth defect that affects the heart and great vessels, accounts for approximately 1 % of all live births [1], and is responsible for approximately 29 % of non-infectious neonatal deaths. CHD is a multifactorial disease [2], and many environmental events lead to this disease, including maternal conditions such as diabetes mellitus, which results in elevated glycosylated hemoglobin levels and increases the risk 2–3 times higher than that in the normal population [3]. Autoimmune diseases, such as systemic lupus erythematosus and Sjogren syndrome, may also increase the risk of atrioventricular block [4]. Different types of infections also contribute to heart problems, such as varicella and rubella, which result in structural damage to the heart [5,6], and parvoviruses, which lead to heart failure secondary to myocarditis and severe anemia [7]; [8]. Exposure to different chemicals in maternity may also enhance the chances of CHD, and alcohol is one of the most prevalent agents. Other routine drugs, such as misoprostol and isotretinoin, and anticonvulsant agents, such as valproic acid, are associated with CHD [9].

In addition to environmental factors, approximately 30 % of CHD cases are caused by genetic factors (chromosomal abnormality or mutation in a single gene or multiple genes) [10]. The heart is one of the earliest developed organs during embryogenesis, and multiple molecular mechanisms and pathways are involved in its development and function [11]. Unfortunately, to date, the molecular mechanisms responsible for CHDs are largely unknown. About 142 genes have been identified so far in humans to be responsible for CHD (https://chdgene.victorchang.edu.au/). In mouse models, this number is much higher (>400) [12]. During heart development, aberrations in genes encoding transcription factors, chromatin modifiers, extracellular matrix proteins, and signalling pathway transducers may lead to anomalies in heart structure and function [12].

Transcription factors and cofactors seem to be crucial for proper structural development of the heart and its functions. The GATA family is a zinc finger transcription factor, and its role in heart development and cardiogenesis has been well established [13]. Pathogenic mutations in GATA4 have been reported to decrease transcriptional activity, leading to ventricular septal defects and bicuspid aortic valves [14]. Moreover, mutations in GATA4 regulatory genes, such as NEXN, also cause CHD [15]. Mouse knockout models for GATA4/6 fail to develop hearts and generate only second heart field (SHF) progenitor cells [16].

The primary aim of this study was to investigate the causative gene mutations in an extended family suffering from CHD and perform further analysis using in silico tools.

2 Materials & methods

2.1 Subjects recruitment

A four-generation family with CHD features was enrolled in this study at King Abdulaziz University Hospital (KAUH). The clinical features of the patient, physical examination results, and medical records were recorded. This study was approved by the Ethics Committee of the Center of Excellence in Genomic Medicine Research (07-CEGMR-Bioeth-2020). Written informed consent was obtained from all the participants prior to the start of the study. The patient was a male with heart problems. The patient showed an absence of the right pulmonary artery (RPA) and dilated left pulmonary artery (LPA), with multiple major aortopulmonary collateral arteries (MAPCAs) extending to the right lung, the largest originating from the subclavian artery. Unfortunately, the child died at 18 months of age due to cardiac complications.

2.2 Whole exome sequencing & Sanger sequencing

Blood samples were collected and immediately transported to the Center of Excellence in Genomic Medicine Research (CEGMR) for further molecular studies. DNA was extracted using a DNeasy® Blood & Tissue Kit (QIAGEN). The quantity and quality of the DNA were monitored using a Nanodrop™ 2000/2000c spectrophotometer (Thermo Fisher Scientific Waltham, Massachusetts, USA). After ensuring the quality and quantity of the DNA, we performed whole-exome sequencing using NovaSeq6000. In brief, the raw sequencing data folder was copied from Novaseq600 to Aziz-supercomputer for in-house NGS analysis. First, the base calls in the BCL files are converted to FASTQ format using a “bcl2fastq” followed by pre-processing FASTQ files consists of: (i) Removing adapters, (ii) Trimming low-quality bases “<20” and (iii) Filtering short reads” <20 pb”. The fastq files were aligned and mapped to the reference human genome reference UCSC hg19 GRCh37 using the BWA mapping (version 0.7.12) application to generate a SAM file format that was converted to a BAM file, a compressed binary version of a SAM file. The ANNOVAR tool was used to annotate the variants with allele frequencies. Base quality score recalibration (BQSR) was performed before variant calling using GATK-Haplotype Caller in vcf file format, with approximately 40,000 variants in the WES data that could be reduced to 3000 after applying the following filtration criteria: (I) filter out the common variant among populations based on minor allele frequency (MAF 0.001). (II) Variant-based filtration [i) DP > 2; otherwise, it was classified as LowDP. MQ > 40.0; otherwise, it was classified as LowMQ, iii. FS < 60.00; otherwise, it was reported as a high FS, iv. QD > 2.0; otherwise, it was reported as LowQD v. QUAL >10.4139; otherwise, it was reported as LowQUAL]. The Variant Interpreter (illumine) tool was used for the annotation, interpretation, and detection of disease-associated variants. The pathogenicity of detected variants and disease-associated information were extracted from databases such as ClinVar, OMIM, Varsome, and PubMed. In addition to database resources, in silico prediction tools (MutationAssessor SIFT, PolyPhen, MutationTaster, PROVEAN, GeneSplicer, and Human Splicing Finder) were used to evaluate the pathogenicity of missense and splice site variants.

The pathogenic mutation in the gene was confirmed by ABI XL3500 using the Big Dye Terminator® with forward and reverse primers: forward primer sequence, 5-GGAAGCTGCGGCCTACAG-3 and reverse primer sequence, 5-AACAAGAGGCCCTCGACAG-3. BioEdit Sequence Alignment Editor Version 7.2.5 was employed to examine sequencing peaks and interpret the results.

2.3 GATA4 mutation analysis using missense 3D

To predict the structural impact of the missense mutation F184S, we used the Alphafold homology model structure of GATA4 (AF-P43694-F1) [17,18]. The missense3D online program (http://missense3d.bc.ic.ac.uk/missense3d/) was used to evaluate structural alterations in GATA4 due to the F184S mutation [19]; [20].

2.4 Structural analysis of wild type and mutated structures of GATA4

The SwissModel Structure Assessment Online program was used to examine the coordinates of wild-type and mutant GATA4 homology model structures. GATA4 structures were uploaded to the structural assessment and comparison tool to obtain structural details in terms of Ramachandran Plots [[21], [22], [23]], evaluation of model quality at both the global and local levels using MolProbity (Version 4.4) [24], and quality estimation using the QMEANDisCo method [25].

2.5 GATA4 mutation analysis using Mutation Taster, Polymorphism Phenotyping v2 and SIFT

The GATA4 mutation (F184S) was examined using the Mutation Taster online tool (https://www.genecascade.org/MutationTaster2021/#), based on a single-base exchange in the coding sequence c.551T > C using the Ensemble Transcript ID ENST00000335135 [26]. Polymorphism Phenotyping v2 (PolyPhen-2) (http://genetics.bwh.harvard.edu/pph2/) and SIFT (https://sift.bii.a-star.edu.sg/) mutation analysis web tools were used to evaluate the impact of the F184S mutation on GATA4 [27]; [28].

2.6 GATA4 mutation analysis using HOPE

GATA4 F184S mutation analysis was performed using the HOPE online tool (https://www3.cmbi.umcn.nl/hope/input/) and the input supplied for each missense mutation [29]. The annotations for GATA4 were derived from the UniProt entry P43694 (https://www.uniprot.org/uniprot/P43694).

3 Results

The patient with CHD in this family was from a consanguineous marriage, and most of the marriages that took place in this family were consanguineous. This may have led to the transfer of the mutated allele in the patient in the homozygous form, as shown in Fig. 1. The patient had an absence of the right pulmonary artery (RPA) and a dilated left pulmonary artery (LPA), with multiple major aortopulmonary collateral arteries (MAPCAs) extending to the right lung, the largest originating from the subclavian artery. Cardiac complications led to death of the child at 18 months of age.Fig. 1 Pedigree of consanguineous family. The arrow indicates the proband (patient).

Fig. 1

3.1 Whole-exome sequencing and Sanger sequencing

Whole exome sequencing revealed many genes; however, upon applying different bioinformatics tools (SIFT, Polyphen, HOPE, Mutation Tester, etc.) and subsequent filtration, we found GATA4 as the main candidate gene, as the other genes were not involved in cardiogenesis and showed pathogenicity. In GATA4, thymine at nucleotide position 551 was substituted with cytosine (c.551T > C); consequently, the amino acid at position 184 was substituted from Phenylalanine to Serine at position 184 (p.Phe184Ser or p.F184S). Sorting Intolerant From Tolerant (SIFT) tool suggested a score of 0, which suggests deleterious, and Polymorphism Phenotyping (PolyPhen) suggested a score of 0.99, resulting in probable damage. Therefore, both tools predicted the mutation to be highly lethal to protein function and may cause disease. Other GATA4 mutations have also been reported in the literature to cause similar cardiac features. Therefore, Sanger sequencing was performed to confirm this mutation. This mutation was confirmed in the patient in a homozygous state. Both the parents were heterozygous for the mutated allele (Fig. 2).Fig. 2 Shows chromatograms of the family. The patient was homozygous for the allele c.551T > C, while the parents were heterozygous.

Fig. 2

We obtained a homology model for GATA4 from the Alphafold server (Fig. 3) to investigate the structural impact of missense mutations (F184S) on patients with heart disease. First, we examined the structural effects of the F184S missense mutation using a missense 3D tool. According to missense 3D study, missense mutation F184S did not induce structural damage in GATA4.Fig. 3 Wild-type (WT) and mutant (F184S) GATA-4 homology models based on the Swiss-Model server. The color schemes are depicted for the WT GATA-4 homology model based on (A) confidence (gradient), (B) hydrophobicity, (C) polarity, and (D) size of the amino acids. The color schemes are depicted for the mutant GATA-4 (F184S) homology model based on (E) confidence (gradient), (F) hydrophobicity (G) polarity, and (H) size of amino acids. (I) Superimposed structures of the WT and Mutant GATA-4 homology models. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3

Structural assessment of mutant protein structures obtained from missense 3D analysis using the SwissModel Structure Assessment tool showed slight variations in the QMEAN Z scores compared with the wild-type GATA4 structure (Fig. 3A–D).However, the clash scores of the GATA4 F184S mutant and the WT homology models were 6.05 and 0.98, respectively. Importantly, the mutant GATA4 structure had more bad bonds (43/3206) than the wild-type GATA4 homology structure (0/3212) (Fig. 3E–H). However, no significant differences were observed between the wild-type GATA4 structure and the mutant structure (Fig. 3I) in terms of Ramachandran Plots, MolProbity Score, or other metrics studied in the SwissModel structure assessment tool.

The impact of the F184S missense mutation in GATA4 was further studied using online web tools such as PolyPhen-2 (score 0.979), SIFT (score 0.99), Mutation Taster (score 155), and HOPE (functional damage). The PolyPhen-2, SIFT, and Mutation Taster analyses indicated that the F184S missense mutation in GATA4 is probably damaging, whereas the HOPE analysis indicated the functional impairment of DNA binding of transcription factor and zinc-ion binding activities of GATA4 (Table 1).Table 1 GATA4 missense mutation analysis using various cutting-edge online tools as indicated in table below.

Table 1
Missense Mutation in GATA-4	Missense3D Prediction	SwissModel
Structural Assessment	PoyPhen-2	SIFT	HOPE	Mutation Taster Score	
QMEAN	Cβ	Torsion	Solvation	All Atoms	Clash Score	
Wild Type	NA	−14.13	−0.46	−9.20	−16.95	−5.16	0.98	NA	NA	NA	NA	
F184S	Structural Damage was not predicted based on Alphafold GATA-4 homology model	−14.07	−0.55	−9.21	−16.68	−5.21	6.05	0.979 (Sensitivity:0.75; Specificity: 0.96
Based on HumDiv)
0.755 (Sensitivity: 0.77; Specificity: 0.86 based on HumVar)	0.99	Functional Damage (DNA binding transcription factor and Zinc-ion binding activities are impacted)	155	

4 Discussion

CHD remains one of the most common causes of non-infectious deaths in newborns [30]. Causative variants underlying CHD remain unknown in approximately 60 % of the cases [31]. In our study, we performed whole-exome sequencing to identify the underlying causative gene and found a pathogenic mutation, F184S, in GATA4. GATA4 is a zinc finger transcription factor located on chromosome 8p23.1-p22. It has six coding exons, comprises 442 amino acid proteins [32], and is highly expressed in cardiomyocytes at different developmental stages [14]. GATA4 contains two zinc finger domains, two transcriptional activation domains, and one nuclear location-signal domain [33]. Abnormalities in GATA4 during embryogenesis or in adult life cause structural and functional anomalies in the heart, such as ventricular septal defect (VSD), atrial septal defect (ASD), patent ductus arteriosus, endocardial cushion defect, tetralogy of Fallot, and pulmonary stenosis [34]; [35]. In addition, GATA4 forms complexes with other transcriptional factors, such as NKX2-5, SMAD1 and 4, and SRF [36].

The SwissModel server structural assessment and comparison tools indicated that the clash score and bad bonds were significantly increased in the GATA-4 F184S mutant homology structure. Furthermore, the impact of the F184 S missense mutation in GATA4 was evaluated using mutation analysis web tools such as missense 3D, PolyPhen-2, SIFT, Mutation Taster, and HOPE. PolyPhen-2 employs a supervised naïve Bayes classifier trained on annotations, conservation scores, and structural characteristics that describe amino acid substitutions. SIFT predicts whether an amino acid substitution affects protein function based on sequence homology and physical properties of amino acids. SIFT can be applied to naturally occurring non-synonymous polymorphisms and laboratory-induced missense mutations. MutationTaster predicts a variant to be deleterious or benign. The Grantham Matrix, an amino acid substitution matrix [37], was used to assess the physicochemical properties of amino acids and provides a score ranging from 0.0 to 215 based on the degree of difference between the wild-type amino acid (F) and the new amino acid (S) in GATA4.

HOPE is a web-based program that analyzes the structural consequences of point mutations in protein sequences [29]. The missense mutation F184S observed in GATA4 can interfere with the normal function of a cell and exert molecular effects by altering a protein's orthosteric or allosteric positions, interaction with substrates, or stability. HOPE predicted that the F184S missense mutation observed in a patient with CHD affects the binding of GATA4 with the DNA and the Zinc ions, thus potentially impairing the normal function of GATA4 transcription factors.

5 Conclusion

In conclusion, we identified a pathogenic variant of GATA4 that is responsible for CHD. This new variant may shed light on GATA4 function and its interactions with other proteins. Further studies using animal models are needed to identify the associated signalling pathways, better understand the disease, and search for potential gene therapy.

Data availability

The data of this study is available from the corresponding author upon reasonable request.

CRediT authorship contribution statement

Mahmood Rasool: Investigation, Data curation, Conceptualization. Peter Natesan Pushparaj: Software, Formal analysis. Absarul Haque: Writing – review & editing. Ayat Mohammed Shorbaji: Investigation. Loubna Siraj Mira: Validation, Data curation. Sherin Bakhashab: Supervision. Mohamed Nabil Alama: Data curation. Muhammad Farooq: Formal analysis. Sajjad Karim: Formal analysis. Lars Allan Larsen: Writing – review & editing, Supervision.

Declaration of competing interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgement

The authors extend their appreciation to the Deputyship for Research & Innovation, 10.13039/100009950 Ministry of Education in Saudi Arabia, for funding this research work through project number (574 ).
==== Refs
References

1 Aidinidou L. Chatzikyriakidou A. Giannopoulos A. Karpa V. Tzimou I. Aidinidou E. Fidani L. Association of NFKB1, NKX2-5, GATA4 and RANKL gene polymorphisms with sporadic congenital heart disease in Greek patients Balkan J. Med. Genet. 24 1 2021 Jul 27 15 20 10.2478/bjmg-2021-0014 PMID: 34447654; PMCID: PMC8366470
2 Meller C.H. Grinenco S. Aiello H. Córdoba A. Sáenz-Tejeira M.M. Marantz P. Otaño L. Congenital heart disease, prenatal diagnosis and management Arch. Argent. Pediatr. 118 2 2020 Apr e149 e161 10.5546/aap.2020.eng.e149 English, Spanish 32199055
3 Miller J.L. De Veciana M. Turan S. Kush M. Firsttrimester detection of fetal anomalies in pregestational diabetes using nuchal translucency, ductus venosus Doppler, and maternal glycosylated hemoglobin Am. J. Obstet. Gynecol. 208 5 2013 385.e1 385.e8
4 Panaitescu A.M. Nicolaides K. Maternal autoimmune disorders and fetal defects J. Matern. Fetal Neonatal Med. 31 13 2018 1798 1806 28627279
5 Mandelbrot L. Fetal varicella - diagnosis, management, and outcome Prenat. Diagn. 32 6 2012 511 518 22514124
6 Boucoiran I. Castillo E. No. 368-Rubella in pregnancy J. Obstet. Gynaecol. Can. 40 12 2018 1646 1656 30527073
7 Prefumo F. Fichera A. Fratelli N. Sartori E. Fetal anemia: diagnosis and management Best Pract. Res. Clin. Obstet. Gynaecol. 58 2019 Jul 2 14 30718211
8 Keighley C.L. Skrzypek H.J. Wilson A. Bonning M.A. Gilbert G.L. Infections in pregnancy Med. J. Aust. 211 3 2019 Aug 134 141 31271467
9 Weston J. Bromley R. Jackson C.F. Adab N. Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child Cochrane Database Syst. Rev. 11 2016 CD010224
10 Tong Y.F. Mutations of NKX2.5 and GATA4 genes in the development of congenital heart disease Gene 588 1 2016 86 94 27154817
11 Zhang X. Wang J. Wang B. Chen S. Fu Q. Sun K. A novel missense mutation of GATA4 in a Chinese family with congenital heart disease PLoS One 11 7 2016 Jul 8 e0158904
12 Williams K. Carson J. Lo C. Genetics of congenital heart disease Biomolecules 9 12 2019 Dec 16 879 31888141
13 Pikkarainen S. Tokola H. Kerkelä R. Ruskoaho H. GATA transcription factors in the developing and adult heart Cardiovasc. Res. 63 2004 196 207 15249177
14 Li R.G. Xu Y.J. Wang J. Liu X.Y. Yuan F. Huang R.T. Xue S. Li L. Liu H. Li Y.J. GATA4 loss-of-function mutation and the congenitally bicuspid aortic valve Am. J. Cardiol. 121 2018 469 474 29325903
15 Yang F. Zhou L. Wang Q. You X. Li Y. Zhao Y. Han X. Chang Z. He X. Cheng C. Wu C. Wang W.J. Hu F.Y. Zhao T. Li Y. Zhao M. Zheng G.Y. Dong J. Fan C. Yang J. Meng X. Zhang Y. Zhu X. Xiong J. Tian X.L. Cao H. NEXN inhibits GATA4 and leads to atrial septal defects in mice and humans Cardiovasc. Res. 103 2 2014 228 237 10.1093/cvr/cvu134 Epub 2014 May 27. PMID: 24866383; PMCID: PMC4498134 24866383
16 Zhao R. Watt A.J. Battle M.A. Li J. Bondow B.J. Duncan S.A. Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice Dev. Biol. 317 2008 614 619 18400219
17 Jumper J. Evans R. Pritzel A. Green T. Figurnov M. Ronneberger O. Tunyasuvunakool K. Bates R. Žídek A. Potapenko A. Bridgland A. Meyer C. Kohl S.A.A. Ballard A.J. Cowie A. Romera-Paredes B. Nikolov S. Jain R. Adler J. Back T. Petersen S. Reiman D. Clancy E. Zielinski M. Steinegger M. Pacholska M. Berghammer T. Bodenstein S. Silver D. Vinyals O. Senior A.W. Kavukcuoglu K. Kohli P. Hassabis D. Highly accurate protein structure prediction with AlphaFold Nature 596 7873 2021 Aug 583 589 10.1038/s41586-021-03819-2 Epub 2021 Jul 15. PMID: 34265844; PMCID: PMC8371605 34265844
18 Varadi M. Anyango S. Deshpande M. Nair S. Natassia C. Yordanova G. Yuan D. Stroe O. Wood G. Laydon A. Žídek A. Green T. Tunyasuvunakool K. Petersen S. Jumper J. Clancy E. Green R. Vora A. Lutfi M. Figurnov M. Cowie A. Hobbs N. Kohli P. Kleywegt G. Birney E. Hassabis D. Velankar S. AlphaFold Protein Structure Database: massively expanding the structural coverage of protein-sequence space with high-accuracy models Nucleic Acids Res. 50 D1 2022 Jan 7 D439 D444 10.1093/nar/gkab1061 PMID: 34791371; PMCID: PMC8728224 34791371
19 Ittisoponpisan S. Islam S.A. Khanna T. Alhuzimi E. David A. Sternberg M.J.E. Can predicted protein 3D structures provide reliable insights into whether missense variants are disease associated? J. Mol. Biol. 431 2019 2197 2212 30995449
20 Khanna T. Hanna G. Sternberg M.J.E. David A. Missense3D-DB web catalogue: an atom-based analysis and repository of 4M human protein-coding genetic variants Hum. Genet. 140 5 2021 805 812 33502607
21 Ramachandran G.N. Ramakrishnan C. Sasisekharan V. Stereochemistry of polypeptide chain configurations J. Mol. Biol. 7 1963 95 99 13990617
22 Ramachandran G.N. Sasisekharan V. Conformation of polypeptides and proteins Adv. Protein Chem. 23 1968 283 438 4882249
23 Porter L.L. Rose G.D. Redrawing the Ramachandran plot after inclusion of hydrogen-bonding constraints Proc. Natl. Acad. Sci. U. S. A. 108 1 2011 Jan 4 109 113 21148101
24 Chenn V.B. Arendall W.B. Headd J.J. Keedy D.A. Immormino R.M. Kapral G.J. Murray L.W. Richardson J.S. Richardson D.C. Acta Crystallogr. D66 2010 16 21
25 Benkert P. Biasini M. Schwede T. Toward the estimation of the absolute quality of individual protein structure models Bioinformatics 27 2011 343 350 21134891
26 Steinhaus R. Proft S. Schuelke M. Cooper D.N. Schwarz J.M. Seelow D. MutationTaster2021 Nucleic Acids Res. 49 W1 2021 Jul 2 W446 W451 10.1093/nar/gkab266 33893808
27 Adzhubei I.A. Schmidt S. Peshkin L. Ramensky V.E. Gerasimova A. Bork P. Kondrashov A.S. Sunyaev S.R. Nat. Methods 7 4 2010 248 249 20354512
28 Sim N.L. Kumar P. Hu J. Henikoff S. Schneider G. Ng P.C. SIFT web server: predicting effects of amino acid substitutions on proteins Nucleic Acids Res. 40 Web Server issue 2012 Jul W452 W457 10.1093/nar/gks539 Epub 2012 Jun 11. PMID: 22689647; PMCID: PMC3394338 22689647
29 Venselaar H. Te Beek T.A. Kuipers R.K. Hekkelman M.L. Vriend G. Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces BMC Bioinf. 11 2010 Nov 8 548
30 Sadowski S.L. Congenital cardiac disease in the newborn infant: past, present, and future Crit. Care Nurs. Clin. 21 2009 37 48
31 Zaidi S. Brueckner M. Genetics and genomics of congenital heart disease Circ. Res. 120 2017 923 940 28302740
32 Soheili F. Jalili Z. Rahbar M. Khatooni Z. Mashayekhi A. Jafari H. Novel mutation of GATA4 gene in Kurdish population of Iran with nonsyndromic congenital heart septals defects Congenit. Heart Dis. 13 2 2018 Mar 295 304 29377543
33 Chen J. Qi B. Zhao J. Liu W. Duan R. Zhang M. A novel mutation of GATA4 (K300T) associated with familial atrial septal defect Gene 575 2 Pt 2 2016 473 477 26376067
34 McCulley D.J. Black B.L. Transcription factor pathways and congenital heart disease Curr. Top. Dev. Biol. 100 2012 253 277 22449847
35 Rajagopal S.K. Ma Q. Obler D. Shen J. Manichaikul A. Tomita-Mitchell A. Boardman K. Briggs C. Garg V. Srivastava D. Goldmuntz E. Broman K.W. Benson D.W. Smoot L.B. Pu W.T. Spectrum of heart disease associated with murine and human GATA4 mutation J. Mol. Cell. Cardiol. 43 6 2007 Dec 677 685 17643447
36 Brody M.J. Cho E. Mysliwiec M.R. Kim T.G. Carlson C.D. Lee K.H. Lee Y. Lrrc10 is a novel cardiac-specific target gene of Nkx2-5 and GATA4 J. Mol. Cell. Cardiol. 62 2013 237 246 23751912
37 Grantham R. Amino acid difference formular to help explain protein evolution Science 185 1974 862 864 4843792
