Homo sapiens neurexin 1 (NRXN1), transcript variant alpha12, mRNA

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Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids. [Nat Commun. 2023]
Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids.
Sebastian R, Jin K, Pavon N, Bansal R, Potter A, Song Y, Babu J, Gabriel R, Sun Y, Aronow B, et al. Nat Commun. 2023 Jun 24; 14(1):3770. Epub 2023 Jun 24.
Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure. [Genes (Basel). 2022]
Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure.
Rhoades R, Henry B, Prichett D, Fang Y, Teng S. Genes (Basel). 2022 Apr 28; 13(5). Epub 2022 Apr 28.
Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings. [Clin Neurol Neurosurg. 2022]
Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings.
Aksu Uzunhan T, Ayaz A. Clin Neurol Neurosurg. 2022 Mar; 214:107141. Epub 2022 Jan 24.

RefSeq protein product
See the reference protein sequence for neurexin-1 isoform alpha12 precursor (NP_001317022.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide