SCN1A
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SCN1A
Summary
SCN1A is a gene[1]. SCN1A ranks in the top 1% of gene entities by monthly Wikipedia readership (16 views/month).[2]
Key Facts
- SCN1A's instance of is recorded as gene[3].
- SCN1A is a type of protein-coding gene[4].
- SCN1A's Commons category is recorded as SCN1A[5].
- SCN1A's HomoloGene ID is recorded as 21375[6].
- SCN1A's genomic start is recorded as 166845670[7].
- SCN1A's genomic start is recorded as 165984641[8].
- SCN1A's genomic end is recorded as 166149214[9].
- SCN1A's genomic end is recorded as 166984523[10].
- SCN1A's ortholog is recorded as Scn1a[11].
- SCN1A's ortholog is recorded as Scn1a[12].
- SCN1A's ortholog is recorded as para[13].
- SCN1A's encodes is recorded as sodium voltage-gated channel alpha subunit 1[14].
- SCN1A's found in taxon is recorded as Homo sapiens[15].
- SCN1A's chromosome is recorded as human chromosome 2[16].
- SCN1A's genetic association is recorded as epilepsy[17].
- SCN1A's genetic association is recorded as Dravet syndrome[18].
- SCN1A's genetic association is recorded as generalized epilepsy with febrile seizures plus[19].
- SCN1A's strand orientation is recorded as reverse strand[20].
- SCN1A's exact match is recorded as http://identifiers.org/ncbigene/6323[21].
- SCN1A's cytogenetic location is recorded as 2q24.3[22].
- SCN1A's expressed in is recorded as Brodmann area 23[23].
- SCN1A's expressed in is recorded as lateral nuclear group of thalamus[24].
- SCN1A's expressed in is recorded as primary visual cortex[25].
- SCN1A's expressed in is recorded as pons[26].
- SCN1A's expressed in is recorded as right uterine tube[27].
Why It Matters
SCN1A ranks in the top 1% of gene entities by monthly Wikipedia readership (16 views/month).[2] SCN1A is known by 15 alternative names across languages and contexts.[28]