SCN3B
protein-coding gene in the species Homo sapiens
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SCN3B
Summary
SCN3B is a gene[1]. SCN3B ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]
Key Facts
- SCN3B's instance of is recorded as gene[3].
- SCN3B is a type of protein-coding gene[4].
- SCN3B's Commons category is recorded as SCN3B[5].
- SCN3B's HomoloGene ID is recorded as 10176[6].
- SCN3B's genomic start is recorded as 123629187[7].
- SCN3B's genomic start is recorded as 123499895[8].
- SCN3B's genomic end is recorded as 123655244[9].
- SCN3B's genomic end is recorded as 123525952[10].
- SCN3B's ortholog is recorded as Scn3b[11].
- SCN3B's ortholog is recorded as Scn3b[12].
- SCN3B's ortholog is recorded as scn3b[13].
- SCN3B's encodes is recorded as Sodium voltage-gated channel beta subunit 3[14].
- SCN3B's encodes is recorded as Sodium channel subunit beta-3[15].
- SCN3B's found in taxon is recorded as Homo sapiens[16].
- SCN3B's chromosome is recorded as human chromosome 11[17].
- SCN3B's genetic association is recorded as Brugada syndrome 7[18].
- SCN3B's genetic association is recorded as atrial fibrillation[19].
- SCN3B's strand orientation is recorded as reverse strand[20].
- SCN3B's exact match is recorded as http://identifiers.org/ncbigene/55800[21].
- SCN3B's cytogenetic location is recorded as 11q24.1[22].
- SCN3B's expressed in is recorded as middle temporal gyrus[23].
- SCN3B's expressed in is recorded as orbitofrontal cortex[24].
- SCN3B's expressed in is recorded as Brodmann area 46[25].
- SCN3B's expressed in is recorded as entorhinal cortex[26].
- SCN3B's expressed in is recorded as superior frontal gyrus[27].
Why It Matters
SCN3B ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]