Paralogue Annotation for RYR2 residue 1721

Residue details

Gene: RYR2
Reference Sequences: LRG: LRG_402, Ensembl variant: ENST00000366574 / ENSP00000355533
Amino Acid Position: 1721
Reference Amino Acid: M - Methionine
Protein Domain: Cytoplasmic region


Paralogue Variants mapped to RYR2 residue 1721

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR1M1729RMalignant hyperthermiaHigh6 16917943

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 RYR2.



RYR2NKYMPGLLRAGYYDLLIDIHLSSYATARLM>M<NNEYIVPMTEETKSITLFPD------ENKK1745
RYR1DAHLPGPLRAGYYDLLISIHLESACRSRRS>M<LSEYIVPLTPETRAITLFPPGRSTENGHPR1759
RYR3NKYLPGLLRSGFYDLLISIHLASAKERKLM>M<KNEYIIPITSTTRNIRLFPD------ESKR1649
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR2

There are currently no reported variants at residue 1721 for RYR2.