KCNH2
protein-coding gene in the species Homo sapiens
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KCNH2
Summary
KCNH2 is a gene[1].
Key Facts
- KCNH2's instance of is recorded as gene[2].
- KCNH2 is a type of protein-coding gene[3].
- KCNH2's HomoloGene ID is recorded as 201[4].
- KCNH2's genomic start is recorded as 150944961[5].
- KCNH2's genomic start is recorded as 150642049[6].
- KCNH2's genomic end is recorded as 150675403[7].
- KCNH2's genomic end is recorded as 150978321[8].
- KCNH2's ortholog is recorded as Kcnh2[9].
- KCNH2's ortholog is recorded as Kcnh2[10].
- KCNH2's ortholog is recorded as kcnh2a[11].
- KCNH2's encodes is recorded as Potassium voltage-gated channel subfamily H member 2[12].
- KCNH2's found in taxon is recorded as Homo sapiens[13].
- KCNH2's chromosome is recorded as human chromosome 7[14].
- KCNH2's genetic association is recorded as short QT syndrome[15].
- KCNH2's genetic association is recorded as long QT syndrome[16].
- KCNH2's genetic association is recorded as atrial fibrillation[17].
- KCNH2's genetic association is recorded as heart arrhythmia[18].
- KCNH2's genetic association is recorded as Romano–Ward syndrome[19].
- KCNH2's strand orientation is recorded as reverse strand[20].
- KCNH2's exact match is recorded as http://identifiers.org/ncbigene/3757[21].
- KCNH2's cytogenetic location is recorded as 7q36.1[22].
- KCNH2's expressed in is recorded as apex of heart[23].
- KCNH2's expressed in is recorded as right auricle of heart[24].
- KCNH2's expressed in is recorded as left ventricle[25].
- KCNH2's expressed in is recorded as muscle layer of sigmoid colon[26].