KCNH5
protein-coding gene in the species Homo sapiens
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KCNH5
Summary
KCNH5 is a gene[1]. KCNH5 ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]
Key Facts
- KCNH5's instance of is recorded as gene[3].
- KCNH5 is a type of protein-coding gene[4].
- KCNH5's HomoloGene ID is recorded as 15858[5].
- KCNH5's ortholog is recorded as Kcnh5[6].
- KCNH5's ortholog is recorded as Kcnh5[7].
- KCNH5's ortholog is recorded as kcnh5a[8].
- KCNH5's encodes is recorded as Potassium voltage-gated channel subfamily H member 5[9].
- KCNH5's found in taxon is recorded as Homo sapiens[10].
- KCNH5's genetic association is recorded as major depressive disorder[11].
- KCNH5's genetic association is recorded as unipolar depression[12].
- KCNH5's exact match is recorded as http://identifiers.org/ncbigene/27133[13].
- KCNH5's cytogenetic location is recorded as 14q23.2[14].
- KCNH5's expressed in is recorded as secondary oocyte[15].
- KCNH5's expressed in is recorded as retinal pigment epithelium[16].
- KCNH5's expressed in is recorded as prefrontal cortex[17].
- KCNH5's expressed in is recorded as Brodmann area 9[18].
- KCNH5's expressed in is recorded as superior frontal gyrus[19].
- KCNH5's expressed in is recorded as Brodmann area 46[20].
- KCNH5's expressed in is recorded as Brodmann area 23[21].
- KCNH5's expressed in is recorded as postcentral gyrus[22].
- KCNH5's expressed in is recorded as hypothalamus[23].
- KCNH5's expressed in is recorded as corpus callosum[24].
Why It Matters
KCNH5 ranks in the top 2% of gene entities by monthly Wikipedia readership (10 views/month).[2]