Paralogue Annotation for RYR1 residue 2454

Residue details

Gene: RYR1
Reference Sequences: Ensembl variant: ENST00000359596 / ENSP00000352608
Amino Acid Position: 2454
Reference Amino Acid: R - Arginine
Protein Domain:


Paralogue Variants mapped to RYR1 residue 2454

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR2R2420WCatecholaminergic polymorphic ventricular tachycarHigh9 19926015, 24025405, 24136861

To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in RYR1.



RYR1SFYAALIDLLGRCAPEMHLIQAGKGEALRI>R<AILRSLVPLEDLVGIISLPLQIPTLGKDGA2484
RYR2TFYSALIDLLGRCAPEMHLIHAGKGEAIRI>R<SILRSLIPLGDLVGVISIAFQMPTIAKDGN2450
RYR3SFYSALIDLLGRCAPEMHLIQTGKGEAIRI>R<SILRSLVPTEDLVGIISIPLKLPSLNKDGS2347
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR1

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.R2454Cc.7360C>T Other MyopathySIFT:
Polyphen:
ReportsOther Myopathy Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in vitro contracture test. Hum Mol Genet. 1999 8(11):2055-62. 10484775
p.R2454Hc.7361G>A Other MyopathySIFT:
Polyphen:
ReportsOther Myopathy Mutation screening of the RYR1 gene and identification of two novel mutations in Italian malignant hyperthermia families. J Med Genet. 1999 36(2):115-8. 10051009
Other Myopathy Functional characterization of ryanodine receptor (RYR1) sequence variants using a metabolic assay in immortalized B-lymphocytes. Hum Mutat. 2009 30(4):E575-90. 19191333
Other Myopathy Genetic variation in RYR1 and malignant hyperthermia phenotypes. Br J Anaesth. 2009 103(4):538-48. doi: 10.1093/bja/aep204. 19648156
Unknown Clinical utility gene card for: Multi-minicore disease. Eur J Hum Genet. 2012 20(2). doi: 10.1038/ejhg.2011.180. 22009146