Homo sapiens multiple EGF like domains 10 (MEGF10), transcript variant - Nucleotide

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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 alternative splicing
See 10 reference mRNA sequence splice variants for the MEGF10 gene.
RefSeq protein product
See the reference protein sequence for multiple epidermal growth factor-like domains protein 10 isoform b precursor (NP_001295050.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens multiple EGF like domains 10 (MEGF10), transcript variant 4, mRNA
Homo sapiens multiple EGF like domains 10 (MEGF10), transcript variant 4, mRNA
gi|1889699909|ref|NM_001308121.2|

Nucleotide

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Nucleotide