STXBP1
protein-coding gene in the species Homo sapiens
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STXBP1
Summary
STXBP1 is a gene[1]. STXBP1 ranks in the top 1% of gene entities by monthly Wikipedia readership (130 views/month).[2]
Key Facts
- STXBP1's instance of is recorded as gene[3].
- STXBP1 is a type of protein-coding gene[4].
- STXBP1's HomoloGene ID is recorded as 2382[5].
- STXBP1's genomic start is recorded as 127579370[6].
- STXBP1's genomic start is recorded as 130374544[7].
- STXBP1's genomic end is recorded as 130457460[8].
- STXBP1's genomic end is recorded as 127696027[9].
- STXBP1's ortholog is recorded as Stxbp1[10].
- STXBP1's ortholog is recorded as Stxbp1[11].
- STXBP1's ortholog is recorded as stxbp1a[12].
- STXBP1's ortholog is recorded as unc-18[13].
- STXBP1's ortholog is recorded as Rop[14].
- STXBP1's encodes is recorded as Syntaxin binding protein 1[15].
- STXBP1's encodes is recorded as Syntaxin-binding protein 1[16].
- STXBP1's found in taxon is recorded as Homo sapiens[17].
- STXBP1's chromosome is recorded as human chromosome 9[18].
- STXBP1's genetic association is recorded as infancy electroclinical syndrome[19].
- STXBP1's genetic association is recorded as Dravet syndrome[20].
- STXBP1's strand orientation is recorded as forward strand[21].
- STXBP1's exact match is recorded as http://identifiers.org/ncbigene/6812[22].
- STXBP1's cytogenetic location is recorded as 9q34.11[23].
- STXBP1's expressed in is recorded as middle temporal gyrus[24].
- STXBP1's expressed in is recorded as lateral nuclear group of thalamus[25].
- STXBP1's expressed in is recorded as Brodmann area 23[26].
- STXBP1's expressed in is recorded as pons[27].
Why It Matters
STXBP1 ranks in the top 1% of gene entities by monthly Wikipedia readership (130 views/month).[2] STXBP1 has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] STXBP1 is known by 8 alternative names across languages and contexts.[29]