iBet uBet web content aggregator. Adding the entire web to your favor.

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.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...
Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

RYR2 Variant and Sudden Death in Patients With Dilated Cardiomyopathy. [J Am Coll Cardiol. 2024]
RYR2 Variant and Sudden Death in Patients With Dilated Cardiomyopathy.
Ben-Haim Y, Bird M, Johnson D, Mohiddin S, Favaloro L, Dyrberg Andersen J, Sheppard MN, Pittman A, Futema M, Behr ER. J Am Coll Cardiol. 2024 Mar 19; 83(11):1105-1107.
Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene. [Front Endocrinol (Lausanne). 2...]
Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene.
Bansal V, Winkelmann BR, Dietrich JW, Boehm BO. Front Endocrinol (Lausanne). 2024; 15:1258982. Epub 2024 Feb 20.
Calcium Signaling Consequences of RyR2-S4938F Mutation Expressed in Human iPSC-Derived Cardiomyocytes. [Int J Mol Sci. 2023]
Calcium Signaling Consequences of RyR2-S4938F Mutation Expressed in Human iPSC-Derived Cardiomyocytes.
Toth N, Zhang XH, Zamaro A, Morad M. Int J Mol Sci. 2023 Oct 18; 24(20). Epub 2023 Oct 18.

RefSeq alternative splicing
See 31 reference mRNA sequence splice variants for the RYR2 gene.
RefSeq protein product
See the reference protein sequence for ryanodine receptor 2 (NP_001026.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
Full text in PMC
Free full text articles in PMC
Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
Probe
Related Probe entry
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
Order TALEN/CRISPR clone [GeneCopoeia Inc.]
Order TALEN/CRISPR clone
GeneCopoeia Inc.
Order qPCR primer [GeneCopoeia Inc.]
Order qPCR primer
GeneCopoeia Inc.
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
GeneCopoeia Inc.
UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser

Homo sapiens ryanodine receptor 2 (RYR2), mRNA
Homo sapiens ryanodine receptor 2 (RYR2), mRNA
gi|1519313221|ref|NM_001035.3|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide