netrin-G2 isoform X8 [Homo sapiens]

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Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. [Am J Hum Genet. 2019]
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
Dias CM, Punetha J, Zheng C, Mazaheri N, Rad A, Efthymiou S, Petersen A, Dehghani M, Pehlivan D, Partlow JN, et al. Am J Hum Genet. 2019 Nov 7; 105(5):1048-1056. Epub 2019 Oct 24.
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features. [Neurogenetics. 2019]
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features.
Abu-Libdeh B, Ashhab M, Shahrour M, Daana M, Dudin A, Elpeleg O, Edvardson S, Harel T. Neurogenetics. 2019 Oct; 20(4):209-213. Epub 2019 Aug 2.
Crystal structure of the ligand binding domain of netrin G2. [J Mol Biol. 2011]
Crystal structure of the ligand binding domain of netrin G2.
Brasch J, Harrison OJ, Ahlsen G, Liu Q, Shapiro L. J Mol Biol. 2011 Dec 16; 414(5):723-34. Epub 2011 Oct 25.

RefSeq mRNA
See reference mRNA sequence for the NTNG2 gene (XM_011519112.3).
RefSeq protein isoforms
See 51 reference sequence protein isoforms for the NTNG2 gene.

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Mus musculus 10 days neonate skin cDNA, RIKEN full-length enriched library, clon...
Mus musculus 10 days neonate skin cDNA, RIKEN full-length enriched library, clone:4732474C02 product:RIKEN cDNA E130106L15 gene, full insert sequence
gi|26081098|dbj|AK028953.1|

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