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Whole exome sequencing identifies a rare variant in DAAM2 as a potential candidate in idiopathic pulmonary ossification

   
@article{ATM26415,
	author = {Sheng-Wen Sun and Mei Zhou and Long Chen and Jiang-Hua Wu and Zhao-Ji Meng and Shuai-Ying Miao and Hong-Li Han and Chen-Chen Zhu and Xian-Zhi Xiong},
	title = {Whole exome sequencing identifies a rare variant in  DAAM2  as a potential candidate in idiopathic pulmonary ossification},
	journal = {Annals of Translational Medicine},
	volume = {7},
	number = {14},
	year = {2019},
	keywords = {},
	abstract = {Background: Diffuse pulmonary ossification (DPO) is a rare disease characterized by bone tissue formation in the lung. DPO can be classified into idiopathic pulmonary ossification (IPO) and secondary pulmonary ossification. Cases with no identified etiology are classified as IPO. Variants of dishevelled associated activator of morphogenesis 2 (DAAM2) have been reported to be involved in the bone-resorption of osteoclasts.
Methods: Whole exome sequencing (WES) was used on samples from a patient with IPO and his healthy parents. The effects of all variants were determined using functional predictors (PolyPhen-2, SIFT, FATHMM and MutationTaster); variants existing only in the patient were further screened compared with his healthy parents. 
Results: Forty deleterious variants, including 25 single nucleotide variants (SNVs) and 15 insertions and deletions (indels), were identified by WES. Finally, DAAM2 (c.G2960T:p.R987L) was screened by pathway analysis. 
Conclusions: We identified a novel variant of DAAM2 (c.G2960T:p.R987L) that might participate in the disease process of IPO.},
	issn = {2305-5847},	url = {https://atm.amegroups.org/article/view/26415}
}