Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis
| العنوان: | Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis |
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| المؤلفون: | Hina Iqbal, Zubair Anwar, Farida Anjum, Asif Mir, Tayyba Sarfaraz |
| المصدر: | Journal of Biomedicine and Biotechnology, Vol 2011 (2011) Journal of Biomedicine and Biotechnology |
| بيانات النشر: | Hindawi Limited, 2011. |
| سنة النشر: | 2011 |
| مصطلحات موضوعية: | Male, Models, Molecular, Health, Toxicology and Mutagenesis, Mutant, DNA Mutational Analysis, lcsh:Medicine, Missense mutation, Child, Conserved Sequence, Genetics, General Medicine, Middle Aged, Pedigree, Chromosomes, Human, Pair 1, Mutation (genetic algorithm), Molecular Medicine, Female, medicine.symptom, Biotechnology, Research Article, Adult, Article Subject, Adolescent, Hearing loss, Hearing Loss, Sensorineural, lcsh:Biotechnology, Molecular Sequence Data, Mutation, Missense, Biology, Bartter syndrome, Young Adult, Genetic linkage, Chloride Channels, lcsh:TP248.13-248.65, medicine, Humans, Family, Amino Acid Sequence, Molecular Biology, Aged, CLCNKB, Base Sequence, Genetic heterogeneity, lcsh:R, Computational Biology, medicine.disease, Haplotypes, biology.protein, Lod Score |
| الوصف: | Nonsyndromic hearing loss is a paradigm of genetic heterogeneity with 85 loci and 39 nuclear disease genes reported so far. Mutations of BSND have been shown to cause Bartter syndrome type IV, characterized by significant renal abnormalities and deafness and nonsyndromic nearing loss. We studied a Pakistani consanguineous family. Clinical examinations of affected individuals did not reveal the presence of any associated signs, which are hallmarks of the Bartter syndrome type IV. Linkage analysis identified an area of 18.36 Mb shared by all affected individuals between markers D1S2706 and D1S1596. A maximum two-point LOD score of 2.55 with markers D1S2700 and multipoint LOD score of 3.42 with marker D1S1661 were obtained. BSND mutation, that is, p.I12T, cosegregated in all extant members of our pedigree. BSND mutations can cause nonsyndromic hearing loss, and it is a second report for this mutation. The respected protein, that is, BSND, was first modeled, and then, the identified mutation was further analyzed by using different bioinformatics tools; finally, this protein and its mutant was docked with CLCNKB and REN, interactions of BSND, respectively. |
| وصف الملف: | text/xhtml |
| اللغة: | English |
| تدمد: | 1110-7251 1110-7243 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e289ec4394515d6f9f5171fee2b832caTest https://doaj.org/article/c200ea95cbc249b7b3e6e8c9bb416173Test |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....e289ec4394515d6f9f5171fee2b832ca |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 11107251 11107243 |
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