KCNQ1
protein-coding gene in the species Homo sapiens
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KCNQ1
Summary
KCNQ1 is a gene[1]. KCNQ1 ranks in the top 1% of gene entities by monthly Wikipedia readership (58 views/month).[2]
Key Facts
- KCNQ1's instance of is recorded as gene[3].
- KCNQ1 is a type of protein-coding gene[4].
- KCNQ1's HomoloGene ID is recorded as 85014[5].
- KCNQ1's genomic start is recorded as 2444684[6].
- KCNQ1's genomic start is recorded as 2465914[7].
- KCNQ1's genomic end is recorded as 2870339[8].
- KCNQ1's genomic end is recorded as 2849105[9].
- KCNQ1's ortholog is recorded as Kcnq1[10].
- KCNQ1's ortholog is recorded as Kcnq1[11].
- KCNQ1's ortholog is recorded as kqt-3[12].
- KCNQ1's ortholog is recorded as kcnq1.1[13].
- KCNQ1's encodes is recorded as Potassium voltage-gated channel subfamily Q member 1[14].
- KCNQ1's found in taxon is recorded as Homo sapiens[15].
- KCNQ1's chromosome is recorded as human chromosome 11[16].
- KCNQ1's genetic association is recorded as type 2 diabetes[17].
- KCNQ1's genetic association is recorded as familial atrial fibrillation[18].
- KCNQ1's genetic association is recorded as long QT syndrome[19].
- KCNQ1's genetic association is recorded as Jervell-Lange Nielsen syndrome[20].
- KCNQ1's genetic association is recorded as Romano–Ward syndrome[21].
- KCNQ1's genetic association is recorded as short QT syndrome[22].
- KCNQ1's strand orientation is recorded as forward strand[23].
- KCNQ1's exact match is recorded as http://identifiers.org/ncbigene/3784[24].
- KCNQ1's cytogenetic location is recorded as 11p15.5-p15.4[25].
- KCNQ1's expressed in is recorded as left adrenal cortex[26].
- KCNQ1's expressed in is recorded as right adrenal cortex[27].
Why It Matters
KCNQ1 ranks in the top 1% of gene entities by monthly Wikipedia readership (58 views/month).[2] KCNQ1 is known by 14 alternative names across languages and contexts.[28]