Literature DB >> 35179696

Identification of causative gene mutation in an Iranian family with coloboma and nephropathy using whole exome sequencing.

Emran Esmaeilzadeh1, Zhila Ghaderi1, Arman Moradi2, Hamid Reza Khorram Khorshid3,4.   

Abstract

Pathogenic variants in FAT1 gene have recently been described in association with coloboma, nephropathy, and facial dismorphism. Here we describe a 5-year-old Iranian boy with iris coloboma and nephropathy, born to an Iranian family. Extracted genomic DNA from blood sample was used to perform whole exome sequencing in the patient. The mutational screening revealed a homozygote Fat1 gene mutation c.5320A > G (p.17747Val), not previously reported in homozygote state in Iran. Our findings establish FAT1 as a gene with pleiotropic effects in human, emphasizing it as one of the causative genes in syndromic nephropathies.
© 2022. The Author(s) under exclusive licence to The Japan Society of Nephrology.

Entities:  

Keywords:  Coloboma; FAT1; Nephropathy; Whole exome sequencing

Year:  2022        PMID: 35179696     DOI: 10.1007/s13730-022-00692-4

Source DB:  PubMed          Journal:  CEN Case Rep        ISSN: 2192-4449


  1 in total

1.  Comparative integromics on FAT1, FAT2, FAT3 and FAT4.

Authors:  Yuriko Katoh; Masaru Katoh
Journal:  Int J Mol Med       Date:  2006-09       Impact factor: 4.101

  1 in total

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