RecName: Full=Multiple epidermal growth factor-like domains protein 10 - Protein

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[A family with early onset myopathy caused by MEGF10 gene defect and literature review]. [Zhonghua Er Ke Za Zhi. 2023]
[A family with early onset myopathy caused by MEGF10 gene defect and literature review].
Lin YF, Wu XY, Yang L, Cheng GQ, Huang Y, Zhuang DY. Zhonghua Er Ke Za Zhi. 2023 Mar 2; 61(3):261-265.
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course. [Acta Myol. 2022]
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course.
Croci C, Traverso M, Baratto S, Iacomino M, Pedemonte M, Caroli F, Scala M, Bruno C, Fiorillo C. Acta Myol. 2022; 41(3):111-116. Epub 2022 Sep 30.
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. [Genes (Basel). 2021]
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.
AlMuhaizea M, Dabbagh O, AlQudairy H, AlHargan A, Alotaibi W, Sami R, AlOtaibi R, Ali MM, AlHindi H, Colak D, et al. Genes (Basel). 2021 Nov 10; 12(11). Epub 2021 Nov 10.

RefSeq genomic sequence
See the genomic reference sequence for the MEGF10 gene (NG_032072.3).
RefSeq protein isoforms
See 10 reference sequence protein isoforms for the MEGF10 gene.

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Q96KG7 [Domain Mapping of Disease Mut...]
Q96KG7
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome

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Protein