Paralogue Annotation for RYR2 residue 4775

Residue details

Gene: RYR2
Reference Sequences: LRG: LRG_402, Ensembl variant: ENST00000366574 / ENSP00000355533
Amino Acid Position: 4775
Reference Amino Acid: A - Alanine
Protein Domain: Transmembrane region


Paralogue Variants mapped to RYR2 residue 4775

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
RYR1A4846VMyotonic dystrophy, type 1High9 17204054

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.



RYR2DIAMGFKTLRTILSSVTHNGKQLVLTVGLL>A<VVVYLYTVVAFNFFRKFYNKSEDGDTPDMK4805
RYR1DIAMGVKTLRTILSSVTHNGKQLVMTVGLL>A<VVVYLYTVVAFNFFRKFYNKSEDEDEPDMK4876
RYR3DIAMGFKTLRTILSSVTHNGKQLVLTVGLL>A<VVVYLYTVVAFNFFRKFYNKSEDDDEPDMK4708
cons                              > <                              

See full Alignment of Paralogues


Known Variants in RYR2

There are currently no reported variants at residue 4775 for RYR2.