RYR1

Summary

RYR1 is a gene^[1]. RYR1 ranks in the top 2% of gene entities by monthly Wikipedia readership (40 views/month).^[2]

Key Facts

• RYR1's instance of is recorded as gene^[3].
• RYR1 is a type of protein-coding gene^[4].
• RYR1's HomoloGene ID is recorded as 68069^[5].
• RYR1's genomic start is recorded as 38924339^[6].
• RYR1's genomic start is recorded as 38433691^[7].
• RYR1's genomic end is recorded as 39078204^[8].
• RYR1's genomic end is recorded as 38595273^[9].
• RYR1's ortholog is recorded as Ryr1^[10].
• RYR1's ortholog is recorded as Ryr1^[11].
• RYR1's ortholog is recorded as ryr1b^[12].
• RYR1's ortholog is recorded as RyR^[13].
• RYR1's encodes is recorded as Ryanodine receptor 1^[14].
• RYR1's found in taxon is recorded as Homo sapiens^[15].
• RYR1's chromosome is recorded as human chromosome 19^[16].
• RYR1's genetic association is recorded as malignant hyperthermia^[17].
• RYR1's genetic association is recorded as malignant hyperthermia, susceptibility to, 1^[18].
• RYR1's genetic association is recorded as central core myopathy^[19].
• RYR1's genetic association is recorded as congenital multicore myopathy with external ophthalmoplegia^[20].
• RYR1's genetic association is recorded as moderate multiminicore disease with hand involvement^[21].
• RYR1's genetic association is recorded as multiminicore myopathy^[22].
• RYR1's genetic association is recorded as King-Denborough syndrome^[23].
• RYR1's strand orientation is recorded as forward strand^[24].
• RYR1's exact match is recorded as http://identifiers.org/ncbigene/6261^[25].
• RYR1's cytogenetic location is recorded as 19q13.2^[26].
• RYR1's expressed in is recorded as glutes^[27].

Why It Matters

RYR1 ranks in the top 2% of gene entities by monthly Wikipedia readership (40 views/month).^[2] RYR1 is known by 10 alternative names across languages and contexts.^[28]