Homo sapiens isolate Y188-sister2 NALCN protein (NALCN) gene, exon 15 - Nucleotide

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.

New insights into the physiology and pathophysiology of the atypical sodium leak channel NALCN. [Physiol Rev. 2024]
New insights into the physiology and pathophysiology of the atypical sodium leak channel NALCN.
Monteil A, Guérineau NC, Gil-Nagel A, Parra-Diaz P, Lory P, Senatore A. Physiol Rev. 2024 Jan 1; 104(1):399-472. Epub 2023 Aug 24.
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection. [Neurol Sci. 2023]
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection.
Tehrani Fateh S, Bagheri S, Sadeghi H, Salehpour S, Fazeli Bavandpour F, Sadeghi B, Jamshidi S, Tonekaboni SH, Mirfakhraie R, Miryounesi M, et al. Neurol Sci. 2023 Dec; 44(12):4491-4498. Epub 2023 Jul 15.
Novel variant c.1838A>G, p.(Gln613Arg) in NALCNcauses camptodactyly and cognitive delay. [Clin Dysmorphol. 2022]
Novel variant c.1838A>G, p.(Gln613Arg) in NALCNcauses camptodactyly and cognitive delay.
Singh P, Agrawal N, Maurya RK, Moirangthem A. Clin Dysmorphol. 2022 Oct 1; 31(4):206-210. Epub 2022 Jun 27.

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the NALCN gene.

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide