SCN5A

Summary

SCN5A is a gene^[1]. SCN5A ranks in the top 1% of gene entities by monthly Wikipedia readership (89 views/month).^[2]

Key Facts

• SCN5A's instance of is recorded as gene^[3].
• SCN5A is a type of protein-coding gene^[4].
• SCN5A's HomoloGene ID is recorded as 22738^[5].
• SCN5A's genomic start is recorded as 38548057^[6].
• SCN5A's genomic start is recorded as 38589548^[7].
• SCN5A's genomic end is recorded as 38691164^[8].
• SCN5A's genomic end is recorded as 38649687^[9].
• SCN5A's ortholog is recorded as Scn5a^[10].
• SCN5A's ortholog is recorded as Scn5a^[11].
• SCN5A's ortholog is recorded as scn5lab^[12].
• SCN5A's ortholog is recorded as scn12aa^[13].
• SCN5A's ortholog is recorded as para^[14].
• SCN5A's encodes is recorded as Sodium voltage-gated channel alpha subunit 5^[15].
• SCN5A's found in taxon is recorded as Homo sapiens^[16].
• SCN5A's chromosome is recorded as human chromosome 3^[17].
• SCN5A's genetic association is recorded as long QT syndrome 3^[18].
• SCN5A's genetic association is recorded as Brugada syndrome 1^[19].
• SCN5A's genetic association is recorded as sudden infant death syndrome^[20].
• SCN5A's genetic association is recorded as dilated cardiomyopathy 1E^[21].
• SCN5A's genetic association is recorded as atrial fibrillation^[22].
• SCN5A's genetic association is recorded as heart conduction disease^[23].
• SCN5A's genetic association is recorded as heart arrhythmia^[24].
• SCN5A's genetic association is recorded as idiopathic ventricular fibrillation, non Brugada type^[25].
• SCN5A's genetic association is recorded as Romano–Ward syndrome^[26].
• SCN5A's genetic association is recorded as progressive familial heart block^[27].

Why It Matters

SCN5A ranks in the top 1% of gene entities by monthly Wikipedia readership (89 views/month).^[2] SCN5A has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.^[28] SCN5A is known by 16 alternative names across languages and contexts.^[29]