In silico analysis of nonsynonymous single‐nucleotide polymorphisms (nsSNPs) of the SMPX gene-Reference-Cited by-同舟云学术

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In silico analysis of nonsynonymous single‐nucleotide polymorphisms (nsSNPs) of the SMPX gene

Published:2019-10-03 Issue:1 Volume:84 Page:54-71
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Arifuzzaman Md.¹^ORCID,Mitra Sarmistha²^ORCID,Das Raju³^ORCID,Hamza Amir⁴^ORCID,Absar Nurul³,Dash Raju⁵^ORCID

Affiliation:

1. College of Pharmacy Yeungnam University Gyeongbuk Republic of Korea

2. Plasma Bioscience Research Center, Plasma‐Bio Display Kwangwoon University Seoul Republic of Korea

3. Department of Biochemistry and Biotechnology University of Science & Technology Chittagong Chittagong Bangladesh

4. Department of Biochemistry Hallym University Gangwon Republic of Korea

5. Department of Anatomy Dongguk University Graduate School of Medicine Gyeongju Republic of Korea

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12350

Reference128 articles.

1. A Novel Deletion inSMPXCauses a Rare form of X-Linked Progressive Hearing Loss in Two Families Due to a Founder Effect

2. In-Silico Computing of the Most Deleterious nsSNPs in HBA1 Gene

3. The rs61742690 (S783N) single nucleotide polymorphism is a suitable target for disrupting BCL11A-mediated foetal-to-adult globin switching

4. Predicting Functional Effect of Human Missense Mutations Using PolyPhen‐2

5. A method and server for predicting damaging missense mutations

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1. Mutational analysis and prediction of the potential impact of missense mutations in the HOXA9 gene in B-cell acute lymphoblastic leukemia;Human Gene;2024-09

2. Computational Exploration of Single-Nucleotide Polymorphisms in the Human hRAS Gene: Implications and Insights;Cureus;2024-01-28

3. Identification of Diseases caused by non-Synonymous Single Nucleotide Polymorphism using Random Forest and Linear Regression Algorithms;2023-06-26

4. The pathogenic effect of SNPs on structure and function of human TLR4 using a computational approach;Journal of Biomolecular Structure and Dynamics;2023-01-17

5. DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research;Frontiers in Genetics;2023-01-06

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