HGNC:6289 Q86W47 8047 KCNN1 HGNC:6290 Q92952 8048 KCNN2 HGNC:6291 Q9H2S1 8049 KCNN3 HGNC:6292 Q9UGI6 8050 KCNN4 HGNC:6293 O15554 8051 KCNQ1 HGNC:6294 P51787...
277 KB (17 words) - 15:46, 9 May 2024
Maxi-K, KCNMA1) KCa2.x: KCa2.1 (KCNN1) - SK1, KCa2.2 (KCNN2) - SK2, KCa2.3 (KCNN3) - SK3 KCa3.x: KCa3.1 (KCNN4) - SK4 KCa4.x: KCa4.1 (KCNT1) - SLACK, KCa4...
19 KB (1,692 words) - 03:53, 29 November 2023
disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3". Mol. Psychiatry. 6 (5): 565–9. doi:10.1038/sj.mp.4000898. PMID 11526470...
3 KB (395 words) - 01:30, 4 March 2023
Subtypes of SK Channels KCa2.1 (SK1, KCNN1) KCa2.2 (SK2, KCNN2) KCa2.3 (SK3, KCNN3) KCa4.1 (Slack, Slo2.2, KCNT1) KCa4.2 (Slick, Slo2.1, KCNT2) KCa5.1 (Slo3...
16 KB (2,067 words) - 23:40, 2 December 2023
KCNN1 Kca2.1 calmodulin, PP2A, CK2 SK2 KCNN2 Kca2.2 calmodulin, PP2A, CK2 SK3 KCNN3 Kca2.3 calmodulin, PP2A, CK2 SK4 KCNN4 Kca3.1 calmodulin, PP2A, CK2...
24 KB (2,730 words) - 07:06, 16 August 2022
"Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies". European Journal of Human Genetics. 29...
16 KB (1,748 words) - 00:08, 17 July 2024