Human dihydropyridine-sensitive L-type calcium channel alpha-1 subunit - 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.

Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth. [Prenat Diagn. 2023]
Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth.
Seed E, Noon F, Milnes D, Roscioli T, Kristensen K, Ellwood D, DaSilva Costa F. Prenat Diagn. 2023 Dec; 43(13):1678-1681. Epub 2023 Dec 18.
CACNA1S Variant Associated With a Myalgic Myopathy Phenotype. [Neurology. 2023]
CACNA1S Variant Associated With a Myalgic Myopathy Phenotype.
Periviita V, Palmio J, Jokela M, Hartikainen P, Vihola A, Rauramaa T, Udd B. Neurology. 2023 Oct 31; 101(18):e1779-e1786. Epub 2023 Sep 7.
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature. [Genes (Basel). 2023]
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.
Marinella G, Orsini A, Scacciati M, Costa E, Santangelo A, Astrea G, Frosini S, Pasquariello R, Rubegni A, Sgherri G, et al. Genes (Basel). 2023 Jun 28; 14(7). Epub 2023 Jun 28.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the CACNA1S gene.

reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
GeneCopoeia Inc.

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide