Homo sapiens membrane metalloendopeptidase (MME), transcript variant 4 - Nucleotide

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A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing. [J Peripher Nerv Syst. 2024]
A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing.
Grosz BR, Parmar JM, Ellis M, Bryen S, Simons C, Reis ALM, Stevanovski I, Deveson IW, Nicholson G, Laing N, et al. J Peripher Nerv Syst. 2024 Jun; 29(2):262-274. Epub 2024 Jun 11.
"Evaluation of neprilysin activity in Adipose-Derived stem cells from Alzheimer's disease patients". [Neurosci Lett. 2024]
"Evaluation of neprilysin activity in Adipose-Derived stem cells from Alzheimer's disease patients".
Shigematsu K, Komori N, Ideno M, Yamagishi H. Neurosci Lett. 2024 Mar 10; 825:137705. Epub 2024 Feb 28.
miRNA-211-5p inhibition enhances the protective effect of hucMSC-derived exosome in Aβ(1-40) -induced SH-SY5Y cells by increasing NEP expression. [J Biochem Mol Toxicol. 2024]
miRNA-211-5p inhibition enhances the protective effect of hucMSC-derived exosome in Aβ(1-40) -induced SH-SY5Y cells by increasing NEP expression.
Chen H, Huang Z, Lei A, Yu X, Shen M, Wu D. J Biochem Mol Toxicol. 2024 Jan; 38(1):e23624.

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the MME gene.
RefSeq protein product
See the reference protein sequence for neprilysin isoform a (NP_001341572.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide