Human ryanodine receptor mRNA, complete cds

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.

Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy. [Int J Mol Sci. 2024]
Compound Heterozygous RYR1 Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive RYR1-Related Myopathy.
Janßen S, Erbe LS, Kneifel M, Vorgerd M, Döring K, Lubieniecki KP, Lubieniecka JM, Gerding WM, Casadei N, Güttsches AK, et al. Int J Mol Sci. 2024 Oct 9; 25(19). Epub 2024 Oct 9.
Individuals and Families Affected by RYR1-Related Diseases: The Patient/Caregiver Perspective. [J Neuromuscul Dis. 2024]
Individuals and Families Affected by RYR1-Related Diseases: The Patient/Caregiver Perspective.
van de Camp SAJH, Stinissen L, Huseth A, Simon B, Ryan J, Sarkozy A, Van Petegem F, Goldberg MF, Jungbluth H, Böhm J, et al. J Neuromuscul Dis. 2024; 11(5):1067-1083.
Lethal multiple pterygium syndrome, large cystic hygroma, and cleft palate: Rare and severe fetal presentations of RYR1- and NEB-related congenital myopathies. [Prenat Diagn. 2024]
Lethal multiple pterygium syndrome, large cystic hygroma, and cleft palate: Rare and severe fetal presentations of RYR1- and NEB-related congenital myopathies.
Jackson M, Thomas MA, Suchet I, Mahallati H, Kuret V, Lauzon J. Prenat Diagn. 2024 Apr; 44(4):522-526. Epub 2024 Mar 23.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the RYR1 gene.

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide