PREDICTED: Homo sapiens leucine rich repeat LGI family member 4 (LGI4) - Nucleotide

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Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations. [Glia. 2021]
Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations.
Booth DG, Kozar N, Bradley S, Meijer D. Glia. 2021 Nov; 69(11):2605-2617. Epub 2021 Jul 21.
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. [Am J Hum Genet. 2017]
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita.
Xue S, Maluenda J, Marguet F, Shboul M, Quevarec L, Bonnard C, Ng AY, Tohari S, Tan TT, Kong MK, et al. Am J Hum Genet. 2017 Apr 6; 100(4):659-665. Epub 2017 Mar 16.
Intratumoral heterogeneity of ADAM23 promotes tumor growth and metastasis through LGI4 and nitric oxide signals. [Oncogene. 2015]
Intratumoral heterogeneity of ADAM23 promotes tumor growth and metastasis through LGI4 and nitric oxide signals.
Costa ET, Barnabé GF, Li M, Dias AA, Machado TR, Asprino PF, Cavalher FP, Ferreira EN, Del Mar Inda M, Nagai MH, et al. Oncogene. 2015 Mar 5; 34(10):1270-9. Epub 2014 Mar 24.

RefSeq protein product
See the reference protein sequence for leucine-rich repeat LGI family member 4 isoform X1 (XP_016881919.1).

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Nucleotide