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. 2019 Nov 11;176(Suppl 1):S142–S228. doi: 10.1111/bph.14749
Nomenclature http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=522 http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=523 http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=524 http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=525 http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=526 http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=527
Common abbreviation THIK2 THIK1 TASK5 TALK1 TALK2 TRESK
HGNC, UniProt https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:6274, http://www.uniprot.org/uniprot/Q9HB15 https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:6275, http://www.uniprot.org/uniprot/Q9HB14 https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:13814, http://www.uniprot.org/uniprot/Q9H427 https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:14464, http://www.uniprot.org/uniprot/Q96T55 https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:14465, http://www.uniprot.org/uniprot/Q96T54 https://www.genenames.org/data/gene‐symbol‐report/#!/hgnc_id/HGNC:19439, http://www.uniprot.org/uniprot/Q7Z418
Endogenous inhibitors http://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=2391 (studied at 10‐50 μM) [http://www.ncbi.nlm.nih.gov/pubmed/12754259?dopt=AbstractPlus]
Inhibitors http://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=2401 (studied at 5 mM) [http://www.ncbi.nlm.nih.gov/pubmed/25148687?dopt=AbstractPlus]
Functional Characteristics Does not function as a homodimer [http://www.ncbi.nlm.nih.gov/pubmed/11060316?dopt=AbstractPlus] but can form a functional heterodimer with K2P13 [http://www.ncbi.nlm.nih.gov/pubmed/25148687?dopt=AbstractPlus]. Background current Unknown Background current Background current Background current
Comments Forms a heterodimer with K2P12 [http://www.ncbi.nlm.nih.gov/pubmed/25148687?dopt=AbstractPlus]. K2P16.1 current is increased by alkaline pHo with a pKa of 7.8 [http://www.ncbi.nlm.nih.gov/pubmed/14985088?dopt=AbstractPlus]. K2P17.1 current is increased by alkaline pHo with a pKa of 8.8 [http://www.ncbi.nlm.nih.gov/pubmed/14985088?dopt=AbstractPlus]. A frame‐shift mutation (F139WfsX24) in the KCNK18 gene, is associated with migraine with aura in humans [http://www.ncbi.nlm.nih.gov/pubmed/20871611?dopt=AbstractPlus].